Nervous system of man
The nervous system lets the body detect stimuli, process the information and respond quickly. This unit follows a message from receptor to effector: the structure and types of neuron, the reflex arc, the nerve impulse and the synapse, then the brain, spinal cord and nerves, the sense receptors, the effects of drugs and pain medicines, nervous disorders and the tests used to diagnose them.
Learning outcomes (32)
- Recognize receptors as transducers sensitive to various stimuli.
- Trace the path of a message transmitted to the CNS (central nervous system) for processing.
- Identify the three neurons (sensory, intermediate, motor) involved in nervous transmission.
- Identify muscles and glands as the effectors.
- Annotate the detailed structure of a sensory neuron, associative and motor neuron.
- Relate the structure of neurons with functions.
- Differentiate between myelinated and non-myelinated neurons.
- Explain the function of the three types of neurons with the help of a reflex arc.
- Define nerve impulse.
- Describe the generation and transmission of nerve impulse.
- Name the factors responsible for the resting membrane potential of neuron.
- Evaluate from a graph the phenomena of polarization, depolarization and hyperpolarization of membrane.
- Compare the velocities of nerve impulse in the axon membrane and in the synaptic cleft.
- Describe the role of local circuits in saltatory conduction of nerve impulse.
- Outline the structure of synapse.
- Explain synaptic transmission of nerve impulse.
- Classify neurotransmitters as inhibitory and excitatory and list some common examples.
- Identify the main components of the nervous system.
- Explain briefly the major parts, functions of major divisions of the brain and its functions.
- Describe the architecture of human brain.
- Describe cranial and spinal nerves in man.
- Explain the structure, types and functions of the autonomic nervous system.
- Explain the structure and functioning of the receptors for smell, taste, and touch/pain.
- Define narcotic drugs as agents that interact with normal nervous activity.
- Compare the use and abuse of drugs with respect to heroine, Cannabis, nicotine, alcohol and inhalants like nail polish remover and glue.
- Explain the terms drug addiction and drug tolerance with reference to caffeine and nicotine and their adverse effects.
- Associate the effects of drug addiction and tolerance with the functioning of the nervous system.
- Describe the way how pain medicines can reduce or numb pain in the human body.
- Discuss that certain pain medications are addictive.
- Classify nervous disorders into vascular, infectious, structural, functional and degenerative disorders.
- Describe the causes, symptoms and treatment of one type of each category of disorders outlined above (e.g., stroke as vascular, meningitis as infectious, brain tumor as structural, headache as functional, and Alzheimer disease as degenerative disorder).
- Explain the principles of important diagnostic tests for nervous disorders i.e., EEG, CT scan and MRI.
The nervous system
The body of an animal is frequently exposed to a variety of stimuli in its daily life. To respond to a particular stimulus, usually more than one body part is involved, and their activities are coordinated either by the nervous system or the endocrine system or both.
- Nervous system
- The system of the body that provides coordination through electric signals among different body parts for the response to a particular stimulus.
- Neurology
- The study of the structure and functions of the nervous system. The term comes from "neuron" (nerve) and "logia" (the study of).
The human nervous system is the most evolved among all the animals. Nervous coordination in higher animals consists of three basic steps.
- Reception of the stimulus by receptors.
- Processing or analysis of the information by the nervous system.
- Response to the stimulus by an effector.
5.1Receptors are transducersOften examined
A transducer is an electronic device that converts energy from one form to another. A cell that responds to a stimulus is called a receptor cell. Receptor cells are transducers: they convert energy from one form such as light, heat or sound into energy in an electrical impulse (electrochemical energy) within a sensory neuron. So receptors are transducers sensitive to various stimuli.
- Transducer
- A device or cell that converts energy from one form to another.
- Receptor cell
- A cell that responds to a stimulus.
Receptors are biological transducers that convert energy from both the external and internal environments into electrical impulses. They may be massed together to form a sense organ, such as the eye or ear, or they may be scattered, as are those of the skin and viscera.
5.2Path of a message transmitted to the central nervous system
Sensory information travels from the body to the spinal cord before reaching the brain. The path is a relay of three neurons, named by their order along the pathway.
| Neuron | Where it lies | What it does |
|---|---|---|
| First-order neuron (sensory or afferent neuron) | From the periphery (skin, muscles or organs) to the CNS | The initial neuron of a sensory pathway. Detects stimuli (touch, pain, temperature) and relays the information to the second-order neuron, usually in the spinal cord or brainstem. |
| Second-order neuron (interneuron) | Usually in the spinal cord or brainstem | Receives input from the first-order neuron, processes it, may integrate it with other sensory inputs, and sends it to higher brain centres (such as the thalamus) or directly to the brain regions involved in perception. |
| Third-order neuron | Thalamus to cortex | Picks up the impulses from the thalamus and relays them to the somatosensory portion of the cerebrum. |
In the pain pathway, the second-order neuron may be located in the dorsal horn of the spinal cord, where it receives signals from the first-order neurons and then projects to the thalamus. Somatosensory sensations are pressure, pain, temperature and the body's senses.
5.3NeuronOften examined
Nervous coordination mainly comprises highly specialized cells called neurons (new-ronz). Neurons are the basic structural and functional unit of the nervous system.
Structure of neuron (5.3.1)
Although neurons vary considerably in size and shape, they all have three basic components: a cell body, dendrites and an axon.
Cell body
The cell body is the main part of a neuron. It contains a mass of granular cytoplasm and a cell membrane. The single large nucleus is centrally placed with a prominent nucleolus. Golgi apparatus, mitochondria and other organelles are present. The cytoplasm is characterised by the presence of Nissl's granules, which are groups of ribosomes and rough ER associated with protein synthesis.
Dendrites
Dendrites are short and thin, often highly branched cytoplasmic extensions that gradually taper from their bases to their tips. Axons of other neurons form synapses with the dendrites. The function of the dendrite is to receive stimuli and conduct impulses to the cell body.
Axon
An axon is comparatively a long and thick nerve fibre which has a constant diameter and can vary in size from a few mm to more than a metre in length. It may be branched or un-branched. Axons terminate by branching to form small extensions with enlarged ends called presynaptic terminals. Functionally, axons conduct action potentials from the neuron cell body to the presynaptic terminals, that is, they conduct the signal (information) away from the cell body.
| Part | Structure | Function |
|---|---|---|
| Cell body (soma) | Granular cytoplasm, cell membrane, a large central nucleus with nucleolus, Golgi apparatus, mitochondria, Nissl's granules | Main part of the neuron; Nissl's granules make proteins |
| Dendrites | Short, thin, highly branched and tapering cytoplasmic extensions | Receive stimuli and conduct impulses to the cell body |
| Axon | Long, thick fibre of constant diameter (a few mm to over 1 m), branched or un-branched, ending in presynaptic terminals | Conducts action potentials away from the cell body to the presynaptic terminals |
- Neuron
- A highly specialised cell that is the basic structural and functional unit of the nervous system.
- Nissl's granules
- Groups of ribosomes and rough ER in the cytoplasm of the cell body, associated with protein synthesis.
- Presynaptic terminals
- The small extensions with enlarged ends at which an axon terminates.
Use the position of each leader line: a structure inside the cell body, a branched process, the long fibre, the white wrapping, the gap between wrappings and the branched end.
| Letter | Structure | Function |
|---|---|---|
| A | Nucleus | Controls the whole neuron |
| B | Dendrite | Receives stimuli and conducts impulses to the cell body |
| C | Axon | Conducts the impulse away from the cell body (here to the axon terminal) |
| D | Myelin sheath | Insulates the axon and speeds up the signal |
| E | Schwann cell | Produces the myelin sheath that wraps the axon |
| F | Axon terminal | Forms junctions (synapses) with other cells |
5.3.2Types of neuronOften examined
All neurons vary somewhat in size, shape and characteristics depending on the function and role of the neuron. Based upon the function there are three types of neurons: sensory neurons, motor neurons and interneurons.
| Type | Structure | Function |
|---|---|---|
| Sensory neuron | Pseudo-unipolar | Converts signals received from the environment into corresponding stimuli. The sensory inputs activate the sensory neurons, which carry sensory information to the brain and spinal cord. |
| Motor neuron | Multipolar; located in the CNS, with the axon extending outside the CNS. The most common type of neuron | Transmits information from the brain to the effector (muscles or gland) of the body. |
| Interneuron | Multipolar; the axons connect only to the nearby sensory and motor neurons | Helps in passing signals between two neurons. |
Types of neuron based on structure
Neurons can also be classified by the number of processes that leave the cell body. Fig. 5.4 shows four kinds.
| Structural type | Processes from the cell body |
|---|---|
| Anaxonic | Many processes that look alike; no distinct axon |
| Bipolar | Two processes, one at each end of the cell body |
| Unipolar | A single process that divides into two branches (sensory neurons are described in the book as unipolar or pseudo-unipolar) |
| Multipolar | Many dendrites and one axon (motor neurons and interneurons) |
5.3.3Effectors
The two examples of effectors are muscles and glands. The nervous system responds by sending signals to muscles and glands. The signals cause muscles to contract. The signals cause glands to produce secretions. Muscles and glands are called effectors because they cause an effect in response to directions from the nervous system.
- Effector
- A muscle or gland that responds to the signals of the nervous system (muscles contract, glands secrete).
5.3.4Detailed structure of a sensory neuron, associative and motor neuronOften examined
a. Sensory neurons (afferent neurons)
The cell body or soma is located in the dorsal root ganglion outside the CNS. Sensory neurons often have their cell bodies close to the spinal cord. Dendrites are specialized extensions that receive signals from sensory receptors. They are often long in peripheral sensory neurons. The axon extends from the sensory receptors to the CNS. In some cases they may be myelinated to speed up the signal transmission.
Most sensory neurons are unipolar, having a single elevated process that branches into two. One branch connects to the sensory receptors and the other branch connects to the CNS. The signal pathway starts from the sensory receptor, moves along the axon and reaches the spinal cord or brain where further processing occurs.
b. Motor neurons (efferent neurons)
The cell body is located in the spinal cord (for lower motor neurons) or in the brain's cortex (for upper motor neurons). Motor neurons have many dendrites that receive inputs from interneurons and other neurons. The axon is long and often myelinated to allow rapid signal transmission from the CNS to the muscles or glands. Most motor neurons are multipolar. Motor neurons transmit signals from the CNS to muscles and glands, allowing for movement and glandular response.
c. Interneurons
The cell body is located entirely within the brain and spinal cord. Dendrites are highly branched to receive information from multiple neurons, making them important for processing complex information. Their axons are generally short and unmyelinated, as they primarily transmit signals locally within the CNS. An interneuron is often multipolar, which allows it to communicate with many neurons simultaneously. Interneurons serve as connectors between sensory and motor neurons. They are critical in reflexes, neural processing and communication within the CNS.
5.3.5Relate the structure of neurons with functionsOften examined
The structure of each type of neuron is intricately designed to support its specific function within the nervous system, ensuring efficient communication and response mechanisms. Fig. 5.8 relates each part of a neuron to its function.
Structure and function of each type
- Motor neurons have long axons, which are essential for covering the considerable distances between the central nervous system and the target muscles or organs. The axons are myelinated, which enhances the speed of signal transmission, allowing the rapid communication necessary for quick muscle responses.
- Sensory neurons possess long dendrites and axons, which are vital for receiving signals from sensory receptors and transmitting them over distances to the central nervous system. Sensory neurons are myelinated and often located in ganglia, which are clusters of neuron cell bodies. This arrangement aids in processing sensory information and contributes to reflex actions.
- Interneurons are generally shorter than both motor and sensory neurons, which is suitable for their role in local processing. Interneurons have numerous branches of axons and dendrites, allowing them to form multiple connections with other neurons. Their partial myelination and clustering in large groups help to enhance the speed of signal transmission despite their shorter length.
| Neuron type | Function | Structure | Location |
|---|---|---|---|
| Sensory neuron | Transmit sensory information to the CNS | Unipolar, with a long axon; cell body in the dorsal root ganglia | Sensory organs to the CNS |
| Motor neuron | Transmit motor commands from the CNS to muscles | Multipolar, with a long axon; neuromuscular junction | CNS to muscles or glands |
| Interneuron | Relay signals between sensory and motor neuron; involved in processing information | Multipolar, with a short axon and highly branched dendrites | CNS (brain and spinal cord) |
5.3.6Differences between myelinated and non-myelinated neuronsOften examined
The axons may be categorized into myelinated (with sheath) and non-myelinated (without sheath). The myelinated fibres are present in the white part of the brain and also in the spinal cord, while the non-myelinated nerve fibre is present in the autonomic nervous system. Myelinated axons tend to be larger in diameter than the non-myelinated axons.
| Myelinated neuron | Non-myelinated neuron |
|---|---|
| They possess a myelin sheath. | These do not possess a myelin sheath. |
| The Schwann cells show wrapping around the nerve axon. | The Schwann cells do not show wrapping but are only present in the groove. |
| This shows two sheaths in the axis of the cylinder. | This shows only one sheath in the axis of the cylinder. |
| These transfer nerve impulses very fast. | These transfer nerve impulses very slowly. |
| These appear white in their fresh form. | These appear grey in their fresh form. |
| They possess nodes and internodes. | These do not possess nodes and internodes. |
| Nodes of Ranvier are present in these neurons. | Nodes of Ranvier are not present in these. |
| Collateral fibres are produced. | Collateral fibres are not produced. |
5.4Reflex arcOften examined
- Reflex action
- An immediate, automatic and involuntary response to external and internal environmental changes.
- Reflex arc
- The path of the nerve impulse during a reflex action.
A typical reflex arc includes five fundamental parts: receptors, sensory neurons, interneuron, motor neuron and effectors.
- A person unexpectedly touches a hot object. Receptors in the skin of the hand are activated by the heat of the object.
- The receptors stimulate a sensory neuron, which leads to the spinal cord through a spinal nerve. The cell body of the sensory neuron is outside the cord (in the dorsal root ganglion) and the neuron enters a dorsal nerve root of the spinal cord.
- The impulse then crosses a synapse to an interneuron, which lies completely within the cord.
- The impulse travels along the interneuron and then passes across a synapse to the dendrites and cell body of a motor neuron, which lies within the spinal cord.
- The motor neuron eventually branches to form synapses with several muscle cells, that is, an effector.
- The nerve impulses move along the motor neuron to the muscles, which contract. The hand is rapidly removed from the source of heat.
| Part | In the hot-object example |
|---|---|
| Receptor | Pain (heat) receptors in the skin of the hand |
| Sensory neuron | Carries the impulse through the dorsal root into the spinal cord |
| Interneuron | Lies wholly inside the spinal cord and relays the impulse |
| Motor neuron | Cell body in the spinal cord; carries the impulse out to the muscle |
| Effector | Muscle of the arm that contracts and withdraws the hand |
5.5Nerve impulseOften examined
- Nerve impulse
- Information or signal about a stimulus that is transmitted from receptors to the CNS and from the CNS to the effectors. In technical terms, a nerve impulse is a wave of electrochemical changes that travel along the length of a neuron from one end to the other.
Generation and transmission of nerve impulse (5.5.1)
The word "electrochemical" refers to the electrical potential (a capacity to do electrical work) that exists on the neuron membrane. In the case of a neuron, the electrical potential is termed the membrane potential, which is exhibited in two different forms: the Resting Membrane Potential (RMP) and the Active Membrane Potential (AMP).
| Form of membrane potential | State of the neuron | Charge distribution |
|---|---|---|
| Resting membrane potential (RMP) | At rest, not being stimulated (polarised) | Outside more positive than inside; about −70 mV |
| Active membrane potential (AMP, action potential) | Stimulated and conducting an impulse (depolarised, then recovering) | Inside more positive than outside for a short time |
5.5.2Resting membrane potentialOften examined
The resting membrane potential is characterised by a more positive outer surface of the neuron membrane than the inner surface. This state is also referred to as the polarised state and the neuron is supposed to be at rest. This means that there is an unequal distribution of ions on the two sides of the nerve cell membrane. The potential measures about 70 mV, with the inside of the membrane negative with respect to the outside. So the resting membrane potential is expressed as −70 mV, and the minus sign indicates that the inside is negative relative to (compared to) the outside.
It is called a resting membrane potential because it occurs when a membrane is not being stimulated or conducting impulses. The resting membrane potential is established by the following factors.
1. Distribution and active movement of Na⁺ and K⁺ ions
The concentration of potassium (K⁺) is about 30 times greater in the fluid inside the neuron than outside, and the concentration of sodium ions (Na⁺) is nearly 10 times greater in the fluid outside the cell than inside. These ions are continuously moved against their concentration gradient through sodium-potassium pumps by the expenditure of energy. For every two K⁺ that are actively transported inward, three Na⁺ are pumped out. So the inside becomes more negative than the outside of the neuron membrane.
2. Negative organic ions
There are many types of organic compounds in the neuron cytoplasm that also have negative charges. These ions include some amino acids, many proteins and RNA. The presence of these ions in the neuron cytoplasm makes the inside of the neuron more negative than the outside.
3. Leakage of K⁺ ions
The cell membrane of a neuron also has many channel proteins called gates. K⁺ ions leak continuously through the leaky K⁺ gates. This also makes the outside of the neuron more positive than the inside.
| Factor | Effect on the charge of the inside |
|---|---|
| Na⁺-K⁺ pump (3 Na⁺ out, 2 K⁺ in) | Removes more positive charge than it brings in, so the inside becomes more negative |
| Negative organic ions (amino acids, proteins, RNA) | Add negative charge inside the cytoplasm |
| Leakage of K⁺ through leaky K⁺ gates | K⁺ leaves, so the outside is more positive than the inside |
Overall there are more positive charges on the outside than on the inside. This is known as the resting membrane potential. It will be maintained until the membrane is disturbed or stimulated by a sufficiently strong stimulus (threshold), when an action potential will be produced.
5.5.3Active membrane potentialOften examined
The active membrane potential (also called action potential) is characterised by a more positive inside of the neuron than outside (depolarised state). This happens when positive charges tend to move inside the neuron on receiving a particular stimulus. This electrochemical change appears on a short region of the neuron for a brief period of time, followed by the recovery of the polarised state. In this way a wave of action potential begins to move towards the other end of the neuron.
Threshold stimulus
- Threshold stimulus
- A stimulus that is capable of producing an action potential in a neuron.
- Sub-threshold stimulus
- A stimulus that is not capable of exciting the neuron or of raising any response.
Influx of Na⁺ ions (depolarization)
When a neuron fibre is stimulated by a threshold stimulus, it causes the opening of voltage-regulated Na⁺ gates. As a result the Na⁺ gates permit the influx of Na⁺ ions by diffusion. Since more Na⁺ ions enter than leave, the electrical potential of the membrane changes from −70 mV towards zero and then reaches about +50 mV. This reversal of polarity across the two sides of the membrane is called depolarization. This electropositivity inside and electronegativity outside lasts for about one millisecond, until the Na⁺ gates are closed.
Repolarization of neuron fibre
A fraction of a second after the sodium gates open, depolarization of the axon membrane causes the potassium gates to open. Potassium therefore diffuses out of the cell. Since the potassium is positively charged, this makes the inside of the cell more negative and starts the process of repolarization.
Hyperpolarization
At the peak of the action potential, the sodium gates start to close again. Sodium permeability therefore declines. The sodium-potassium pump continues to work during this time, so it gradually begins to restore the original resting potential. This repolarization is shown by the falling phase of the action potential spike and results in the membrane potential returning to its original level. In fact, there is a slight overshoot into a more negative potential than the original resting potential. This is called hyperpolarization. It is due to the slight delay in closing all the potassium gates compared with the sodium gates.
| Phase | Gates | Ion movement | Membrane potential |
|---|---|---|---|
| Resting (polarised) | Na⁺ and K⁺ voltage-regulated gates closed; leaky K⁺ gates open | Pump: 3 Na⁺ out, 2 K⁺ in; K⁺ leaks out | −70 mV, inside negative |
| Depolarization | Voltage-regulated Na⁺ gates open | Na⁺ diffuses in | Rises from −70 mV through zero to about +50 mV; inside positive |
| Repolarization | Na⁺ gates close; K⁺ gates open | K⁺ diffuses out | Falls back towards −70 mV; inside negative again |
| Hyperpolarization | K⁺ gates close a little later than Na⁺ gates | Extra K⁺ lost; pump restores the balance | Slightly below −70 mV, then returns to −70 mV |
Refractory period
After an action potential, the nerve fibre undergoes a period of recovery in which it regains its original ionic distribution and polarity and prepares itself for the next stimulation. This period of recovery of the nerve fibre is called the refractory period. Although a repolarised neuron fibre has the same polarity as that of a polarised neuron fibre, it has a different ionic distribution: it has more K⁺ outside and more Na⁺ inside. So the repolarised nerve fibre undergoes a refractory period of a few milliseconds, during which the original ionic distribution is restored by the sodium-potassium pump, which actively transports Na⁺ ions out and K⁺ ions in. This returns the membrane to its resting potential, that is, −70 mV. The refractory period lasts for about 4 milliseconds, so a neuron can conduct 250 impulses per second.
- (a) Read the dashed lines. The resting potential is −70 mV and the threshold is about −55 mV. The stimulus must raise the potential from −70 mV to −55 mV before the spike starts.
- (b) At 2.0 ms the curve is rising steeply through the threshold: this is depolarization. Voltage-regulated Na⁺ gates open and Na⁺ diffuses in, so the inside is becoming positive.
- At 2.9 ms the curve is at its peak (about +40 mV). The inside is positive. The Na⁺ gates start to close and the K⁺ gates are opening.
- At 4.6 ms the curve is below the resting level (about −79 mV): this is hyperpolarization. K⁺ has been leaving, and the K⁺ gates are slightly slower to close than the Na⁺ gates. The pump then restores −70 mV.
- (c) Each impulse needs 4 ms before the next can start. In one second (1000 ms) the neuron can conduct impulses.
- The pain stimulus acts on the pain receptors and tries to raise the membrane potential of the sensory neuron from −70 mV to the threshold.
- An action potential needs Na⁺ to diffuse in through the voltage-regulated Na⁺ gates. With the gates blocked, Na⁺ cannot enter.
- So the membrane never depolarises. It stays at the resting potential (−70 mV) and no action potential is formed.
- No impulse travels along the neuron, so no pain signal reaches the brain and the patient feels no pain. The resting potential itself is unchanged, because it depends on the pump, the negative organic ions and the leaky K⁺ gates, not on the voltage-regulated gates.
5.5.4Velocities of nerve impulseOften examined
The velocities of nerve impulse in the axon membrane and in the synaptic cleft are variable. In human non-myelinated fibres, nerve impulses travel at 1 to 3 metres per second. Myelinated fibres conduct at speeds of up to 120 metres per second.
| Where the impulse travels | Speed or time |
|---|---|
| Non-myelinated axon (human) | 1 to 3 m per second |
| Myelinated axon | Up to 120 m per second (saltatory conduction, up to 50 times faster than the fastest unmyelinated axons) |
| Synaptic cleft | The short journey across the synapse takes about a millisecond, longer than a nerve impulse takes to travel the same distance (synaptic delay) |
What makes a nerve impulse faster
- Saltatory conduction. The rapid transmission of a nerve impulse along an axon, resulting from the action potential jumping from one node of Ranvier to another, skipping the myelinated regions of membrane. It is up to 50 times faster than conduction through the fastest unmyelinated axons because the impulse does not have to travel through every single space before moving to the next.
- Myelin sheath as an insulator. Myelin acts as an insulating sheath and prevents loss of energy, so myelinated neuron fibres require less energy.
- Diameter of the fibre. Thick neuron fibres conduct impulses faster than thin fibres, because resistance to electrical current flow is inversely proportional to the cross-sectional area of the conductor. With an increase in thickness of the neuron fibre there is a decrease in resistance of the fibre to the nerve impulse.
- Saltatory conduction
- The rapid transmission of a nerve impulse along an axon, resulting from the action potential jumping from one node of Ranvier to another, skipping the myelinated regions of membrane.
- Synaptic delay
- The time of about a millisecond that the short journey across the synapse takes, which is longer than a nerve impulse takes to travel the same distance in an axon.
- Use time = distance ÷ speed.
- (a) Non-myelinated: , .
- (b) Myelinated: .
- Compare the two times. This is the effect of saltatory conduction (impulse jumping from node to node) and of the insulating myelin sheath.
- Each synapse adds a synaptic delay of about 1 ms, so a pathway with one synapse in (b) takes about .
| Fibre | Speed | Time for 1.2 m |
|---|---|---|
| Non-myelinated | 2 m per second | 600 ms |
| Myelinated | 100 m per second | 12 ms |
5.5.5Role of local circuits in saltatory conductionOften examined
- Local circuits
- Circuits of current that create depolarization in the next section of the axon membrane. They play a key role in saltatory conduction, the process by which nerve impulses jump from node to node in myelinated nerve fibres.
Local circuits, or the diffusion of sodium ions along the axon, trigger the depolarization of the next section of the axon membrane. This process causes the action potential to appear and jump from one node of Ranvier to the next.
- At a node the voltage-regulated Na⁺ channels open and Na⁺ enters: this node is at its action potential (node 2).
- The Na⁺ ions diffuse along the inside of the axon, and current returns outside the sheath. This local circuit of current reaches the next node but cannot cross the myelin, which insulates the axon between nodes.
- The next node (node 3) becomes depolarised: its membrane potential moves towards the threshold level, and its Na⁺ channels start to open.
- When the threshold is reached the new node fires. The action potential has therefore "jumped" from node to node.
- Behind the impulse, the node (node 1) is repolarising: its K⁺ channels are open and its Na⁺ channels are closed (refractory period). Ahead of the impulse the node (node 4) is still at resting potential, about −70 mV.
5.6SynapseOften examined
- Synapse
- The junction between the axon terminal of one neuron and the dendrite of another neuron, where information from one neuron is transmitted or relayed (handed over) to another neuron.
Structure of synapse (5.6.1)
The neurons are not in direct contact at a synapse. There is a gap, called the synaptic cleft, between them. A single neuron may form synapses with many incoming fibres of different neurons.
- Presynaptic neuron
- The neuron that carries an impulse toward a synapse.
- Postsynaptic neuron
- The neuron that receives the impulse after it crosses the synapse.
- Synaptic cleft
- The gap between the axon terminal of the presynaptic neuron and the postsynaptic neuron.
| Part of a synapse | What it is |
|---|---|
| Presynaptic neuron | Sends the impulse; its axon ends in rounded synaptic knobs that contain synaptic vesicles |
| Synaptic knob | Rounded swelling at the distal end of the axon (dendrites lack these knobs) |
| Synaptic vesicles | Membranous sacs in the knob that hold the neurotransmitter |
| Synaptic cleft | Gap between the two neurons; the neurons are not in direct contact |
| Postsynaptic neuron | Receives the impulse; its membrane has receptor molecules and ion channels |
5.6.2Mechanism of synaptic transmission of nerve impulseOften examined
The movement of an impulse across the synapse is called synaptic transmission. It takes place by the formation of a message which is transmitted across the synapse in the form of a chemical messenger called a neurotransmitter. The axons usually have several rounded synaptic knobs at their distal ends, which dendrites lack. These knobs contain numerous membranous sacs, called synaptic vesicles, and when a nerve impulse reaches a knob, some of the vesicles respond by releasing a neurotransmitter.
- An action potential arrives at the synaptic knob. Calcium channels open in the presynaptic membrane. As the calcium ion concentration inside the knob is lower than outside, calcium ions rush in. As the calcium concentration increases, synaptic vesicles move towards the membrane.
- The neurotransmitter vesicles fuse with the plasma membrane of the transmitting cell.
- The fused vesicles release their neurotransmitter molecules into the synaptic cleft.
- The released neurotransmitter molecules diffuse across the cleft and bind to receptor molecules on the postsynaptic cell surface membrane.
- Binding of the neurotransmitter to the postsynaptic receptors opens some channels and allows Na⁺ ions to diffuse across the postsynaptic membrane. As a result the postsynaptic membrane depolarises and an action potential is generated. Since this depolarization brings the membrane potential towards threshold level, it is called an excitatory postsynaptic potential (EPSP).
- Once the neurotransmitters have acted on the postsynaptic membrane, they are immediately broken down by enzymes: acetylcholine is hydrolysed by acetylcholinesterase and adrenaline by monoamine oxidase.
- Synaptic transmission
- The movement of an impulse across the synapse, by means of a chemical messenger.
- Neurotransmitter
- A chemical messenger released from the synaptic vesicles that carries the message across the synaptic cleft.
- Excitatory postsynaptic potential (EPSP)
- The depolarization of the postsynaptic membrane towards threshold level caused by the neurotransmitter, which can generate an action potential.
| Step | Where | Why it matters |
|---|---|---|
| Ca²⁺ enters the knob | Presynaptic membrane | Calcium concentration is higher outside, so it flows in and makes the vesicles move to the membrane |
| Vesicles fuse and release | Presynaptic membrane | Puts the neurotransmitter into the cleft |
| Neurotransmitter diffuses and binds | Cleft and postsynaptic membrane | Binding opens ion channels |
| Na⁺ enters | Postsynaptic membrane | Depolarizes the membrane (EPSP) and can start an action potential |
| Enzyme breaks down the neurotransmitter | Cleft | Stops the signal so the membrane can reset |
5.6.3Classifications of neurotransmitters
Neurotransmitters are classified as excitatory and inhibitory.
Excitatory neurotransmitters
Neurotransmitters that cause increased membrane permeability to sodium ions and, thus, trigger nerve impulses are said to be excitatory. Acetylcholine is an excitatory neurotransmitter of the peripheral nervous system, whereas biogenic amines (amino acid derivatives) are important neurotransmitters in the central nervous system. They include epinephrine, norepinephrine, serotonin and dopamine, all of which also function as hormones. Epinephrine and norepinephrine increase the heartbeat rate during stress. Serotonin and dopamine affect sleep, mood, attention and learning.
Inhibitory neurotransmitters
Other neurotransmitters cause decreased membrane permeability to sodium ions, thus causing the threshold of stimulus to be raised. This action is called inhibitory, because it lessens the chance that a nerve impulse will be transferred to an adjoining neuron, for example amino acids gamma-aminobutyric acid (GABA) and glycine. The endorphins are peptides that function as both neurotransmitters and hormones, decreasing our perception of pain.
| Feature | Excitatory | Inhibitory |
|---|---|---|
| Effect on Na⁺ permeability of the postsynaptic membrane | Increased | Decreased |
| Effect on the nerve impulse | Triggers it | Lessens the chance that it will be transferred (threshold is raised) |
| Examples | Acetylcholine (peripheral nervous system); epinephrine, norepinephrine, serotonin and dopamine (biogenic amines in the CNS) | GABA and glycine (amino acids); endorphins (peptides) |
| Functions noted by the book | Epinephrine and norepinephrine: heartbeat rate in stress. Serotonin and dopamine: sleep, mood, attention, learning | Endorphins: decrease the perception of pain |
5.7Main components of nervous systemOften examined
The human nervous system consists of the central nervous system (CNS) and the peripheral nervous system (PNS). The CNS is a coordinating centre and it lies in the midline of the body, whereas the PNS transmits information from receptors to the CNS and transmits orders and commands from the CNS to effectors.
| Division | Parts | Function |
|---|---|---|
| Central nervous system (CNS) | Brain; spinal cord | Brain: receives and processes sensory information, initiates responses, stores memories, generates thoughts and emotions. Spinal cord: conducts signals to and from the brain and controls reflex activities |
| Peripheral nervous system (PNS) | Motor neurons; sensory neurons | Motor neurons: CNS to muscles and glands. Sensory neurons: sensory organs to the CNS |
| Somatic nervous system | Part of the motor side of the PNS | Controls voluntary movements |
| Autonomic nervous system | Part of the motor side of the PNS | Controls involuntary responses; has a sympathetic ("fight or flight") and a parasympathetic ("rest or digest") division |
5.7.1Architecture of human brain and spinal cord and their functionsOften examined
The central nervous system consists of the brain and spinal cord, and both are hollow. The brain and spinal cord are covered with three protective membranes called meninges (singular: meninx). The brain is enclosed within the cranium, while the spinal cord is enclosed within the vertebral column.
- Dura matter (next to the cranium)
- Arachnoid matter (middle membrane)
- Pia matter (next to the nervous tissue)
Between the arachnoid and pia matter there is a fluid, the cerebrospinal fluid (CSF), which helps to cushion the brain from shock.
- Meninges
- The three protective membranes covering the brain and spinal cord: dura matter, arachnoid matter and pia matter.
- Cerebrospinal fluid (CSF)
- The fluid between the arachnoid and pia matter that helps to cushion the brain from shock.
5.7.1The brainOften examined
The brain is divided into three parts: forebrain, midbrain and hindbrain. The forebrain consists of the cerebrum, thalamus and limbic system. The hindbrain consists of the cerebellum, medulla oblongata and pons.
Forebrain
Cerebrum
The cerebrum is the largest part of the human brain. It is divided into two cerebral hemispheres which are interconnected with each other by a band of axons, called the corpus callosum. Each hemisphere contains four surface lobes: frontal, parietal, temporal and occipital lobe.
Each lobe further contains different functional areas, for example auditory (hearing) and visual areas. Each functional area consists of three sub-areas: sensory area, association area and motor area. The sensory area receives impulses from different body parts. The association area interprets or analyses the incoming information. The motor area controls the responses of the body. The cerebrum also functions in the analysis and interpretation of memory, reasoning, judgement, thoughts and dreams.
| Sub-area of a functional area | Function |
|---|---|
| Sensory area | Receives impulses from different body parts |
| Association area | Interprets or analyses the incoming information |
| Motor area | Controls the responses of the body |
Thalamus and limbic system
The thalamus is below the cerebrum. It receives all sensory impulses (except the sense of smell) and channels them to the limbic system and to the appropriate regions of the cortex for interpretation. The limbic system is a complex set of structures that lies on both sides of the thalamus, just under the cerebrum. It includes the hypothalamus, the amygdala, the hippocampus and several other nearby areas.
- Hypothalamus: on the ventral side of the thalamus. It maintains homeostasis and contains centres for regulating hunger, sleep, thirst, body temperature, water balance and blood pressure, menstrual cycle and sleep-wake cycle. It also controls the pituitary gland and thereby serves as a link between the nervous and endocrine system.
- Amygdalae: two almond-shaped masses of neurons on either side of the thalamus. They control feelings and emotions of love, hate, anger, fear, rage and sexual arousal.
- Hippocampus: consists of two "horns" that curve back from the amygdala. It appears to be very important in converting things that are "in your mind" at the moment (in short-term memory) into things that you will remember for the long run (long-term memory).
Midbrain
The midbrain is reduced in humans. It acts as a relay station for tracts passing between the cerebrum and the spinal cord or cerebellum. The midbrain contains the reticular formation, which is a relay centre connecting the hindbrain with the forebrain.
Hindbrain
The hindbrain consists of the cerebellum, medulla oblongata and pons.
- Cerebellum controls equilibrium, that is, body position, and coordination of the actions of individual muscles to produce complex activities such as walking, running, riding bicycles and doing delicate work with the hand. The cerebellum is also involved in learning and memory storage for behaviour.
- Pons acts as a bridge between the cerebellum, medulla and cerebrum. It also controls the rate and pattern of heartbeat and breathing.
- Medulla controls the automatic functions of the body, such as heartbeat, blood pressure, respiration and swallowing.
The brain is a hollow structure as it has cavities called ventricles. There are four ventricles in the brain.
| Part of the brain | Main function |
|---|---|
| Cerebrum | Sensory, association and motor areas; memory, reasoning, judgement, thoughts and dreams |
| Thalamus | Receives all sensory impulses (except smell) and channels them to the limbic system and cortex |
| Hypothalamus | Homeostasis: hunger, sleep, thirst, body temperature, water balance, blood pressure, menstrual cycle, sleep-wake cycle; controls the pituitary gland |
| Amygdalae | Feelings and emotions: love, hate, anger, fear, rage and sexual arousal |
| Hippocampus | Converts short-term memory into long-term memory |
| Midbrain | Relay station between cerebrum, spinal cord and cerebellum; reticular formation |
| Cerebellum | Equilibrium and coordination of muscles; learning and memory storage for behaviour |
| Pons | Bridge between cerebellum, medulla and cerebrum; rate and pattern of heartbeat and breathing |
| Medulla | Automatic functions: heartbeat, blood pressure, respiration, swallowing |
In a cross-section of the brain the cerebral cortex forms the outer grey matter and the cerebral medulla forms the inner white matter. The arrangement of grey and white matter in the brain is opposite to that of the spinal cord.
5.7.1Spinal cordOften examined
The spinal cord is the most important structure between the body and the brain. It extends from the medulla to the level of the lumbar vertebrae. It is a vital link between the brain and the body.
A transverse section of the adult spinal cord shows white matter in the periphery, grey matter inside and a tiny central canal filled with CSF at its centre. The grey matter is shaped like the letter "H" or a "butterfly".
| Feature | Grey matter | White matter |
|---|---|---|
| Position in the spinal cord | Inside, shaped like "H" or a butterfly | Periphery (outside) |
| Made of | Neuron cell bodies and non-myelinated parts of the fibres | Bundles of myelinated fibres |
| Position in the brain | Outside (cerebral cortex) | Inside (cerebral medulla) |
Several pairs of spinal nerves originate from the ventral and dorsal horn of the grey matter. The dorsal root of the spinal nerves also contains ganglia present just beside the spinal cord.
5.7.2Cranial and spinal nerves in manOften examined
Cranial nerves
The peripheral nervous system consists of the nerves that branch out from the central nervous system and connect it to other body parts. The peripheral nervous system includes cranial nerves, which arise from the brain, and spinal nerves, which arise from the spinal cord.
A number of cranial nerves send electrical signals between the brain and different parts of the neck, head and torso. These signals help us to smell, taste, hear and move our facial muscles. The cranial nerves begin toward the back of the brain. There are twelve cranial nerve pairs. Each nerve pair splits to serve the two sides of the brain and body. For example, we have one pair of olfactory nerves: one olfactory nerve is on the left side of the brain and one is on the right side of the brain. The twelve nerves are numbered from I to XII using Roman numerals according to the order in which they emerge from the front of the brain to the back of the brain. The twelve cranial nerves each have a specific function. The cranial nerves have been categorised based on number and function.
| No. | Cranial nerve | Type | Function |
|---|---|---|---|
| I | Olfactory nerve | Sensory | Sense of smell |
| II | Optic nerve | Sensory | Sense of sight |
| III | Oculomotor nerve | Motor | Movement of eyes |
| IV | Trochlear nerve | Motor | Rotation of the eye ball |
| V | Trigeminal nerve | Mixed | Functioning of the facial parts |
| VI | Abducens nerve | Mixed | Rotation of the eye ball |
| VII | Facial nerve | Mixed | Facial expression and sense of taste |
| VIII | Auditory (vestibular) nerve | Sensory | Sense of hearing and balance |
| IX | Glossopharyngeal nerve | Mixed | Ability to taste and swallow |
| X | Vagus nerve | Mixed | Digestion and heart rate |
| XI | Cranial (spinal) accessory nerve | Motor | Shoulder and neck movement |
| XII | Hypoglossal nerve | Motor | Ability to move the tongue |
Spinal nerves
A spinal nerve carries motor, sensory and autonomic signals between the spinal cord and the body. Each spinal nerve is a mixed nerve. It is formed from the combination of nerve root fibres from its dorsal and ventral roots.
There are 31 pairs of spinal nerves, one on each side of the vertebral column. These include eight cervical nerve pairs (nerves starting in the neck and running mostly to face and head), twelve thoracic nerve pairs (nerves in the upper body that extend to chest, upper back and abdomen), five lumbar nerve pairs (nerves in the low back that run to legs and feet), five sacral nerve pairs (nerves in the low back extending into the pelvis) and one pair of coccygeal nerves. The spinal nerves are part of the peripheral nervous system.
| Region | Pairs | Serves (book) |
|---|---|---|
| Cervical | 8 | Neck, running mostly to face and head |
| Thoracic | 12 | Upper body: chest, upper back and abdomen |
| Lumbar | 5 | Low back: legs and feet |
| Sacral | 5 | Low back: extending into the pelvis |
| Coccygeal | 1 | (not described further) |
| Total | 31 |
Outside the vertebral column, the nerve divides into branches. The dorsal ramus contains nerves that serve the posterior portions of the trunk. The ventral ramus contains nerves that serve the remaining anterior parts of the trunk and the upper and lower limbs.
| Feature | Cranial nerves | Spinal nerves |
|---|---|---|
| Arise from | The brain | The spinal cord |
| Number | 12 pairs | 31 pairs |
| Type | Sensory, motor or mixed (see the table) | All are mixed nerves (dorsal root sensory, ventral root motor) |
| Part of | Peripheral nervous system | Peripheral nervous system |
5.7.3Peripheral nervous systemOften examined
The peripheral nervous system can also be subdivided into the somatic and autonomic nervous systems.
Somatic nervous system
Generally, the somatic nervous system consists of the cranial and spinal nerve fibres that connect the CNS to the skin and skeletal muscles; it is involved in conscious activities.
Autonomic nervous system
The autonomic nervous system includes those fibres that connect the CNS to the visceral organs, such as the heart, stomach, intestines and various glands. It is concerned with unconscious activities. The autonomic system is divided into the sympathetic and parasympathetic systems. Both of these systems function automatically and usually subconsciously, in an involuntary manner.
Sympathetic division
The sympathetic division controls various autonomic functions during the state of emergency. It prepares the body for the fight or flight response. It consists of only spinal nerves. These nerves arise from the first thoracic segment to the second lumbar segment of the spinal cord.
Parasympathetic division
A few cranial nerves, including the vagus nerve, together with nerves that arise from the sacral portion of the spinal cord, form the parasympathetic division. It controls various autonomic functions during the state of rest. In short, the parasympathetic system returns the body functions to normal after they have been altered by sympathetic stimulation. In times of danger, the sympathetic system prepares the body for violent activity. The parasympathetic system reverses these changes when the danger is over.
| Feature | Somatic nervous system | Autonomic nervous system |
|---|---|---|
| Connects the CNS to | Skin and skeletal muscles | Visceral organs (heart, stomach, intestines) and glands |
| Nerves | Cranial and spinal nerve fibres | Sympathetic and parasympathetic divisions |
| Kind of activity | Conscious (voluntary movements) | Unconscious (involuntary responses) |
Choose three points the book gives: the state each controls, where its nerves arise, and what it does to the body.
| Point | Sympathetic division | Parasympathetic division |
|---|---|---|
| State controlled | Emergency: "fight or flight" | Rest: "rest or digest" |
| Origin of nerves | Spinal nerves only, from the first thoracic to the second lumbar segment of the cord (T1 to L2) | A few cranial nerves (including the vagus) and nerves from the sacral part of the cord |
| Effect on the body | Prepares the body for violent activity | Returns the body functions to normal and reverses the changes when the danger is over |
5.7.4Sensory receptors and their workingOften examined
The body must detect what is occurring inside and outside the body, and this is performed by sensory receptors. Here we discuss receptors for smell, taste, touch and pain.
Olfactory receptors
The smell or olfactory receptors are chemoreceptors, stimulated by chemicals dissolved in liquids. The olfactory organs, which contain the olfactory receptors, are present in the upper part of the nasal cavity. The olfactory receptor cells are neurons. These cells are surrounded by columnar epithelial cells having cilia at the distal ends. Chemicals that stimulate the olfactory receptors enter the nasal cavity as gases. They must dissolve at least partially in the watery fluids that surround the cilia before they can be detected.
Taste receptors
Taste buds occur primarily on the surface of the tongue and are associated with tiny elevations called papillae. Each taste bud includes a group of modified epithelial cells, the taste cells, which function as receptors. The taste bud has an opening, the taste pore, on its surface. Tiny projections, called taste hairs, protrude from the outer ends of the taste cells and just protrude through the taste pore. There are four primary taste sensations: sweet, sour, salty and bitter, which are situated at various regions on the tongue. All the four regions overlap at certain places.
Sensory receptors in human skin
The dermis of the skin contains receptors for touch, pressure, temperature and pain. Meissner's corpuscles and Merkel disks are touch receptors. These consist of small, oval masses of flattened connective tissue cells. Two or more sensory nerve fibres branch into each corpuscle. Meissner's corpuscles are especially numerous in the lips, fingertips, palm and soles. Paccinian's corpuscles are also encapsulated nerve endings present in the fatty layer deep into the skin. They are concerned with the sensation of pressure. Receptors for touch and pressure are also called mechanoreceptors. The skin also has cold and heat receptors to detect the temperature variations.
Pain receptors are technically called nociceptors. Pain receptors are located at the top of the skin in the epidermis area to detect pain. These receptors are free nerve endings that respond to chemicals released by damaged tissues or excess stimuli of heat or pressure. These receptors are widely distributed throughout the skin and inter tissues, except in the tissue of the brain.
| Receptor | Where | Detects |
|---|---|---|
| Olfactory receptor cells (chemoreceptors) | Upper part of the nasal cavity | Smell: chemicals that dissolve in the watery fluid around the cilia |
| Taste cells in taste buds | Tongue, with papillae | Sweet, sour, salty and bitter (regions overlap) |
| Meissner's corpuscles and Merkel disks | Dermis (Meissner's numerous in lips, fingertips, palm, soles) | Touch |
| Pacinian corpuscles | Fatty layer deep in the skin | Pressure |
| Ruffini endings, Krause end bulbs | Skin | Heat; cold |
| Free nerve endings (nociceptors) | Epidermis | Pain: chemicals from damaged tissue, excess heat or pressure |
5.8Effects of drugs on nervous coordinationOften examined
A narcotic is a group of substances which, when administered, diminish the perception of pain. Narcotics bind to certain painkilling sites in the brain. With constant use, they build up in the brain and block the production of endorphins, the brain's natural painkilling chemicals. Their side effects are inhibition of the endocrine and autonomic nervous system and so on. The narcotics are the drugs that act as agents which interact with normal nervous activity.
- Narcotic drugs
- Drugs that act as agents which interact with normal nervous activity; they diminish the perception of pain by binding to painkilling sites in the brain.
- Endorphins
- The brain's natural painkilling chemicals, whose production is blocked when narcotics build up with constant use.
5.8.1Narcotic drugsOften examined
Common narcotic drugs are heroin, Cannabis, nicotine and alcohol and so on.
Heroin
Heroin gives a feeling of euphoria along with relief of pain. Side effects can include nausea, vomiting, respiratory and circulatory depression leading to death.
Cannabis
It is the dried flowering tops, leaves and stem of the Indian hemp plant Cannabis sativa. It includes marijuana and hashish. Usually the users report a mild euphoria, along with alterations in vision and judgement. Intoxication is recognised by the presence of hallucinations, anxiety and depression.
Nicotine
It is an alkaloid derived from tobacco. When smoking a cigarette, nicotine is quickly distributed to all body organs. In the peripheral nervous system, nicotine stimulates postsynaptic receptors (like acetylcholine) and leads to increased skeletal muscular activity. It also increases heartbeat rate and blood pressure.
Alcohol
Alcohol acts as a depressant and slows down nervous communication. Its short-term effects are impairment of vision, judgement and alertness. Long-term chronic drinking can damage the nervous system, liver and pancreas.
Withdrawal symptoms of alcohol
Individuals who eliminate addictive substances from their lives often feel withdrawal symptoms. Alcohol withdrawal refers to a group of symptoms that may occur from suddenly stopping the use of alcohol. The symptoms are: feeling of anxiety, irritability, depression, headache and hallucinations.
Inhalants
These are volatile organic chemicals, commonly referred to as "glue sniffing". Inhalant abuse now includes aerosols (for example hair spray) and anaesthetics (for example ether). Inhalants rapidly start euphoria followed by central nervous system depression. Deep breathing of the toxic vapours may result in hallucinations or even death.
| Drug | Source or nature | Effects named by the book |
|---|---|---|
| Heroin | Narcotic | Euphoria and relief of pain; side effects: nausea, vomiting, respiratory and circulatory depression leading to death |
| Cannabis | Dried flowering tops, leaves and stem of Indian hemp (Cannabis sativa); marijuana and hashish | Mild euphoria, alterations in vision and judgement; intoxication: hallucinations, anxiety, depression |
| Nicotine | Alkaloid from tobacco | Stimulates postsynaptic receptors (like acetylcholine), increases skeletal muscular activity, heartbeat rate and blood pressure |
| Alcohol | Depressant | Slows nervous communication; short term: impaired vision, judgement and alertness; long term: damage to nervous system, liver and pancreas; withdrawal: anxiety, irritability, depression, headache, hallucinations |
| Inhalants | Volatile organic chemicals (glue, hair spray aerosols, ether) | Rapid euphoria followed by CNS depression; hallucinations or death on deep breathing of vapours |
5.8.2Drug addiction and drug toleranceOften examined
- Drug addiction
- A dependence on an illegal drug or a medication. You may want to quit, but most people find they can't do it on their own.
- Drug tolerance
- A person's diminished response to a drug, which occurs when the drug is used repeatedly and the body adapts to the continued presence of the drug, for example caffeine and nicotine.
a. Caffeine
Caffeine is a drug, and individuals can develop both tolerance and a form of dependence.
- Caffeine tolerance: tolerance to caffeine means that the body becomes accustomed to its effects, requiring higher doses to achieve the same level of alertness or stimulation.
- Caffeine addiction: it does not cause classic addiction the way some drugs do.
- Harmful effects of caffeine: insomnia, rapid heart rate, anxiety, frequent urination, digestive issues, fatigue, high blood pressure and irritability tremors.
b. Nicotine
Nicotine is the chemical in tobacco that makes it hard to quit.
- Nicotine tolerance: it occurs when the body requires increasing amounts of nicotine to achieve the same effects initially felt with lower doses.
- Nicotine addiction: nicotine produces pleasing effects in your brain, but these effects are temporary. So you reach for another cigarette. The more you smoke the more nicotine you need to feel good.
- Harmful effects of nicotine: cancer, nausea, dizziness, emphysema, infertility, insomnia, cardiovascular diseases, headache and mouth ulcer.
| Feature | Caffeine | Nicotine |
|---|---|---|
| Tolerance | Body becomes accustomed to it; higher doses needed for the same alertness | Increasing amounts needed for the same effect that lower doses first gave |
| Addiction | Does not cause classic addiction (a form of dependence) | Pleasing but temporary effects in the brain, so the person reaches for another cigarette |
| Harmful effects | Insomnia, rapid heart rate, anxiety, frequent urination, digestive issues, fatigue, high blood pressure, irritability tremors | Cancer, nausea, dizziness, emphysema, infertility, insomnia, cardiovascular diseases, headache, mouth ulcer |
5.8.3Effects of drug addiction and tolerance on the central nervous system
Drugs are chemicals that interfere with the way neurons normally send, receive and process information. Some drugs can activate neurons because their chemical structure mimics that of a natural neurotransmitter. Drugs interact with the brain and body to alter moods, emotions and behaviours by changing brain chemistry. The regions of the brain affected by drug abuse are the brain stem, limbic system and cerebral cortex.
- Depressants all work by slowing down the functioning of the central nervous system.
- Stimulants can produce a number of effects on the body such as increased heart rate, improved concentration and increased respiratory rate.
| Class | Effect on the central nervous system | Effects named by the book |
|---|---|---|
| Depressants | Slow down the functioning of the CNS | (for example alcohol slows nervous communication) |
| Stimulants | Produce a number of effects on the body | Increased heart rate, improved concentration, increased respiratory rate |
5.9Pain medicines reduce or numb pain in human bodyOften examined
Analgesics are also called painkillers. These medicines reduce or numb pain in the body through various mechanisms that affect the nervous system. There are different types of pain medications and each works in a unique way to interfere with pain signals. The main categories of pain medications and how they function are as follows.
- a. Non-steroid anti-inflammatory drugs (NSAIDs): these medicines work by inhibiting the activity of an enzyme called cyclooxygenase (COX), which plays a key role in the production of prostaglandins. Prostaglandins are chemicals released at the site of injury or inflammation that cause pain, swelling and fever. By reducing the production of prostaglandins, NSAIDs help to reduce inflammation and numb pain.
- b. Acetaminophen (paracetamol): it is believed that it works by acting on the brain's pain centre. It likely inhibits COX enzymes in the brain, which reduces the perception of pain without the anti-inflammatory effect.
- c. Opioids: these are also called narcotics. Opioids bind to opioid receptors in the brain, spinal cord and other parts of the nervous system. These receptors are involved in the transmission and perception of pain. When opioids bind to these receptors they block pain signals from being transmitted to the brain and increase the brain's threshold for pain, essentially dulling or eliminating the sensation of pain.
- d. Local anaesthetics: these work by blocking sodium channels in nerve cells. Sodium channels are essential for the transmission of electric signals along nerves. By blocking these channels, local anaesthetics prevent pain signals from travelling from the site of injury to the brain. These are commonly used for procedures where localised numbing is required, such as dental work or minor surgeries.
- e. Antidepressants and anticonvulsants: these medicines are used to treat chronic pain, particularly nerve pain. They work by modulating the neurotransmitters involved in pain perception, such as serotonin and norepinephrine.
- f. Corticosteroids: they reduce swelling and inflammation, which in turn reduces pain. They work by inhibiting the production of inflammatory chemicals and suppressing the immune response.
- g. Other medicines: these numb a localised area. Some are used to relax muscles.
| Pain medicine | How it works | Where it acts |
|---|---|---|
| NSAIDs | Inhibit cyclooxygenase (COX), so fewer prostaglandins (pain, swelling, fever) | Site of injury or inflammation |
| Acetaminophen (paracetamol) | Probably inhibits COX in the brain; no anti-inflammatory effect | Brain's pain centre |
| Opioids (narcotics) | Bind opioid receptors; block pain signals and raise the brain's pain threshold | Brain, spinal cord and other parts of the nervous system |
| Local anaesthetics | Block sodium channels in nerve cells, so signals cannot travel to the brain | Nerve cells at the site of injury |
| Antidepressants and anticonvulsants | Modulate neurotransmitters (serotonin, norepinephrine) involved in pain perception; for chronic nerve pain | Nervous system |
| Corticosteroids | Inhibit inflammatory chemicals and suppress the immune response | Site of swelling and inflammation |
5.9.1Certain pain medications are addictive
Physicians typically prescribe opioids to manage moderate to severe pain. However, opioids can become addictive because they not only dull pain, but also produce a sense of euphoria (intense happiness). This, combined with tolerance build-up (needing to increase doses to produce the same effect), can lead to opioid use disorder.
Opioids also cause neurons that produce dopamine to respond. Dopamine is a neurotransmitter that plays a role in how we feel pleasure, or strong reactions to something. This creates feelings of euphoria. Physicians reduce the length and strength of opioids to try to prevent addiction.
- Opioids dull pain and produce euphoria.
- The body adapts, so higher doses are needed for the same effect (tolerance).
- Dopamine-producing neurons are affected, which creates feelings of pleasure.
- Pleasure plus rising doses can lead to opioid use disorder (addiction). Physicians therefore reduce the length and strength of opioid treatment.
5.10Disorders of the nervous system
The disorders of the nervous system may be classified as vascular, infectious, structural, functional and degenerative. While classifying, the site of involvement is also considered. The book discusses the causes, symptoms and treatment of a few diseases of the major categories.
| Category | What it means (book) | Example described |
|---|---|---|
| Vascular | Abnormality in blood circulation of the nervous system | Stroke |
| Infectious | Caused by an infectious agent: viruses, bacteria, fungi, protozoa and Platyhelminthes | Meningitis |
| Structural | Disturb the structure of the brain | Tumour |
| Functional | Disorders of the function of the nervous system (the book describes headache under this heading) | Headache |
| Degenerative | Degeneration of different parts of the nervous system without an identifiable external cause; genetic factors are involved | Alzheimer's disease |
5.10.1Vascular disorders of the CNS
Any disorder of the nervous system which occurs due to abnormality in blood circulation is called a vascular disorder of the nervous system, for example strokes and brain haemorrhage.
Stroke
It occurs due to rupture of small cerebral arteries.
- Cause: the cause and risk factors for stroke include hypertension, cigarette smoking, diabetes mellitus, high alcohol intake, thrombosis, blood disorders, blood embolism and cocaine abuse.
- Symptoms: sudden loss of function in one region of the brain. Weakness and heaviness occur in the arm, leg or face. Paralysis occurs on the side of the body opposite the cerebral infarction (a portion of the tissue that is dying because the blood supply to it has been cut off). Aphasia (inability to express through words) may be present.
- Treatment: medical treatment is aimed at preventing further attacks and stroke. Anticoagulants and platelet aggregation inhibitors (such as aspirin) are given. Blood pressure management and nursing care are essential.
- Cerebral infarction
- A portion of the brain tissue that is dying because its blood supply has been cut off.
- Aphasia
- Inability to express through words.
5.10.2Infectious disorders of the CNS
Infections of the central nervous system can be caused by almost any infectious agent, including viruses, bacteria, fungi, protozoa and Platyhelminthes.
Meningitis
It is an inflammation of the meninges.
- Cause: bacterial or viral infection of the meninges.
- Symptoms: usually include stiffness in the neck, headache and fever. In severe cases, meningitis may also cause paralysis, coma or death.
- Treatment: for viral meningitis there is no specific treatment. Bacterial meningitis is treated with antibiotics and steroids.
5.10.3Structural disorders of the CNS
Several disorders disturb the structure of the brain and are referred to as structural disorders, such as tumours.
Tumour
A tumour (tumor) is an abnormal mass of neuroglial cells produced as a result of uncontrolled cell division.
- Cause: it is caused by mutation, which may occur at any age in the brain and spinal cord.
- Symptoms: these vary widely, depending on the location of the tumour, but may include headaches, severe nerve pain, paralysis, seizures, coma and death.
- Treatment: surgical removal of the tumour.
5.10.4Functional disorders of the CNS
Headache
Headache is the pain anywhere in the region of the head or neck. It can be a symptom of a number of different conditions of the head and neck. The brain tissue itself is not sensitive to pain because it lacks pain receptors. Rather, the pain is caused by disturbance of the pain-sensitive structures around the brain.
| Category | Cause | Examples |
|---|---|---|
| Primary headaches | Due to the headache condition itself and not due to another cause | Migraine, tension headache |
| Secondary headaches | Due to an underlying structural problem in the head or neck | Bleeding in the brain, tumour, meningitis and so on |
Treatment: several analgesic drugs are available for the treatment of any kind of headache.
5.10.5Degenerative disorders of the CNS
Many diseases cause degeneration in different parts of the nervous system without an identifiable external cause. Genetic factors are known to be involved. An example of such diseases is Alzheimer's disease.
Alzheimer's disease
Alzheimer's disease is a slowly progressive disease of the brain that is characterised by impairment of memory and eventually by disturbances in reasoning, planning, language and perception. Although the onset of this disease occurs in aged people, it is not particularly associated with ageing.
- Cause: there is genetic predisposition, so it tends to run in families.
- Symptoms: the most prominent symptom is short-term memory loss.
- Treatment: there is no effective treatment for this disease.
| Disease (category) | Cause | Symptoms | Treatment |
|---|---|---|---|
| Stroke (vascular) | Rupture of small cerebral arteries; risk factors: hypertension, smoking, diabetes, high alcohol intake, thrombosis, blood disorders, embolism, cocaine abuse | Sudden loss of function in one region of the brain; weakness; paralysis on the opposite side; aphasia | Prevent further attacks: anticoagulants, aspirin, blood pressure management, nursing care |
| Meningitis (infectious) | Bacterial or viral infection of the meninges | Stiff neck, headache, fever; in severe cases paralysis, coma or death | Viral: no specific treatment. Bacterial: antibiotics and steroids |
| Tumour (structural) | Mutation causing uncontrolled division of neuroglial cells | Headaches, severe nerve pain, paralysis, seizures, coma, death | Surgical removal |
| Headache (functional) | Disturbance of pain-sensitive structures around the brain (primary or secondary) | Pain in the head or neck | Analgesic drugs |
| Alzheimer's disease (degenerative) | Genetic predisposition; runs in families | Short-term memory loss, then disturbed reasoning, planning, language, perception | No effective treatment |
5.11Principles of diagnostic tests for nervous disordersOften examined
These days a number of diagnostic tests have been developed for nervous disorders. The principles of EEG, CT scan and MRI are discussed here.
Electroencephalography (EEG)
Neurons within the cerebral cortex continuously generate electrical activity. This activity can be recorded by electrodes attached to precise locations on the scalp, producing an electroencephalogram, and this technique is called electroencephalography (EEG). An EEG pattern is commonly called brain waves.
Computed Tomography scan (CT scan)
Computerised tomography is more commonly known by its abbreviated name, CT scan. It is an X-ray procedure that combines many X-ray images with the aid of a computer to generate cross-sectional views and, if needed, three-dimensional images of the internal organs and structures of the body. A CT scan is used to define normal and abnormal structures in the body and/or assist in procedures by helping to accurately guide the placement of instruments or treatments.
Magnetic Resonance Imaging (MRI)
A Magnetic Resonance Imaging (MRI) scan is a radiology technique that uses magnetism, radio waves and a computer to produce images of body structures. The MRI scanner is a tube surrounded by a giant circular magnet. The patient is placed on a moveable bed that is inserted into the magnet. The patient is exposed to a strong magnetic field and a beam of radio waves. The receiver information is processed by a computer and an image is produced. The image and resolution produced by MRI is quite detailed and can detect tiny changes of structures within the body.
| Test | Principle | What it records or produces |
|---|---|---|
| EEG | Electrodes on precise locations of the scalp record the electrical activity continuously generated by neurons of the cerebral cortex | Electroencephalogram: EEG pattern (brain waves) |
| CT scan | X-ray source and detectors rotate around the body; a computer combines many X-ray images | Cross-sectional (and if needed 3-D) images, tomograms |
| MRI | Strong magnetic field and a beam of radio waves; receiver signals processed by a computer | Detailed images that can detect tiny changes of structure |
| State | EEG activity | Description |
|---|---|---|
| Fully awake | Alpha and beta | Alpha: medium frequency waves. Beta: irregular low amplitude waves when very alert and attentive |
| Drowsy (transition) | Theta | Transition stage between wakefulness and sleep |
| Sleeping | Irregular theta with sleep spindles (12 to 14 Hz) and K complexes; next stage: delta | Delta: high-amplitude waves, 20 to 50 percent of the time |
STEAM Activity 5.1
Investigating reflex actions
Researchers can carry out a number of investigations to determine the effect of a specific factor on human reaction times. A suitable investigation could be the effect of caffeine or the amount of background noise in the room. A simple method to measure the effect is to use the ruler drop test.
- Work with a partner.
- Person A holds out their hand with a gap between their thumb and first finger.
- Person B holds the ruler with the zero at the top of person A's thumb.
- Person B drops the ruler without telling person A, and person A must catch it.
- The number level with the top of person A's thumb is recorded in a suitable table. Repeat this ten times.
- Swap places and record another ten attempts.
- Use the conversion table to convert your ruler measurements into reaction time, or just record the catch distance in cm.
| Catch distance (cm) | Reaction time (ms) |
|---|---|
| 1 | 50 |
| 5 | 90 |
| 10 | 140 |
| 15 | 170 |
| 20 | 200 |
| 25 | 230 |
| 30 | 250 |
Important: 1 millisecond (ms) is one thousandth of a second (1/1000 s).
Example results
| Attempt | Distance on ruler (cm), with noise | Distance on ruler (cm), without noise |
|---|---|---|
| 1 | 25 | 18 |
| 2 | 38 | 15 |
| 3 | 36 | 22 |
| 4 | 31 | 24 |
| 5 | 38 | 13 |
| Mean | 33.6 | 18.4 |
The mean catch distance is greater with noise (168\div5=33.6 cm) than without noise (92\div5=18.4 cm). A longer catch distance means a slower reaction, so background noise slowed the reaction time. Using the conversion table, 18.4 cm lies between 15 cm (170 ms) and 20 cm (200 ms), so the reaction time without noise is about 190 ms. A catch distance of 33.6 cm is beyond the last value of the table (30 cm, 250 ms), so the reaction time with noise is more than 250 ms.
- Find each mean.\begin{aligned}\bar d_{\text{without}}&=\dfrac{16+18+17+20+19}{5}=\dfrac{90}{5}=18\ \mathrm{cm}\\ \bar d_{\text{with}}&=\dfrac{12+10+14+9+15}{5}=\dfrac{60}{5}=12\ \mathrm{cm}\end{aligned}
- Convert 18 cm. It lies between 15 cm (170 ms) and 20 cm (200 ms). The table rises by 30 ms for every 5 cm, so for 3 cm above 15 cm add \tfrac35\times30=18 ms.170+18=188\ \mathrm{ms}
- Convert 12 cm. It lies between 10 cm (140 ms) and 15 cm (170 ms). For 2 cm above 10 cm add \tfrac25\times30=12 ms.140+12=152\ \mathrm{ms}
- Compare. The difference in reaction time is 188-152=36 ms. In this small sample, caffeine shortened the reaction time, so the student caught the ruler sooner.
| Condition | Mean catch distance (cm) | Reaction time (ms) |
|---|---|---|
| Without caffeine | 18 | 188 |
| With caffeine | 12 | 152 |
Key terms
- Nervous system
- The system of the body that provides coordination through electric signals among different body parts for the response to a stimulus.
- Neuron
- A highly specialised cell that is the basic structural and functional unit of the nervous system; it has a cell body, dendrites and an axon.
- Receptor cell
- A cell that responds to a stimulus; it is a transducer that converts the stimulus energy (light, heat, sound) into an electrical impulse in a sensory neuron.
- Effector
- A muscle or gland that responds to the signals of the nervous system.
- Nissl's granules
- Groups of ribosomes and rough ER in the cell body of a neuron, associated with protein synthesis.
- Dendrites
- Short, thin, branched extensions of a neuron that receive stimuli and conduct impulses to the cell body.
- Axon
- A long, thick nerve fibre of a neuron that conducts action potentials away from the cell body to the presynaptic terminals.
- Sensory neuron
- A neuron that carries sensory information from receptors to the brain and spinal cord (afferent neuron); its cell body is in the dorsal root ganglion.
- Motor neuron
- A multipolar neuron that carries information from the CNS to an effector, a muscle or gland (efferent neuron).
- Interneuron
- A multipolar neuron within the CNS that passes signals between sensory and motor neurons; also called a relay or association neuron.
- Reflex action
- An immediate, automatic and involuntary response to external and internal environmental changes.
- Reflex arc
- The path of the nerve impulse during a reflex action: receptor, sensory neuron, interneuron, motor neuron and effector.
- Nerve impulse
- A wave of electrochemical changes that travels along the length of a neuron from one end to the other.
- Resting membrane potential
- The potential of a neuron that is not conducting an impulse (polarised state): about −70 mV, the inside negative relative to the outside.
- Active membrane potential
- The action potential: a brief state in which the inside of a neuron is more positive than the outside (depolarised state).
- Depolarization
- The reversal of polarity across the membrane (inside becoming positive) caused by the influx of Na⁺ ions through voltage-regulated Na⁺ gates.
- Repolarization
- The return of the inside of the membrane towards negative, as K⁺ ions diffuse out of the cell.
- Hyperpolarization
- A slight overshoot to a potential more negative than the resting potential, because the K⁺ gates close slightly later than the Na⁺ gates.
- Threshold stimulus
- A stimulus that is capable of producing an action potential in a neuron.
- Refractory period
- The recovery period (about 4 ms) after an action potential in which the Na⁺-K⁺ pump restores the original ionic distribution and −70 mV.
- Saltatory conduction
- The rapid transmission of a nerve impulse along a myelinated axon as the action potential jumps from one node of Ranvier to the next.
- Synaptic delay
- The time of about a millisecond that an impulse takes to cross the synapse, longer than it takes to travel the same distance along an axon.
- Local circuits
- Circuits of current that depolarise the next section of the axon membrane and so carry the impulse between nodes in saltatory conduction.
- Synapse
- The junction between the axon terminal of one neuron and the dendrite of another, where information is passed on.
- Synaptic cleft
- The gap between the presynaptic and postsynaptic neurons at a synapse.
- Presynaptic neuron
- The neuron that carries an impulse toward a synapse.
- Postsynaptic neuron
- The neuron that receives the impulse after it crosses the synapse.
- Neurotransmitter
- A chemical messenger released from synaptic vesicles that carries the message across the synaptic cleft.
- Excitatory postsynaptic potential (EPSP)
- The depolarization of the postsynaptic membrane towards threshold, caused by a neurotransmitter opening Na⁺ channels.
- Excitatory neurotransmitter
- A neurotransmitter that increases membrane permeability to Na⁺ and triggers nerve impulses, such as acetylcholine, epinephrine, norepinephrine, serotonin and dopamine.
- Inhibitory neurotransmitter
- A neurotransmitter that decreases membrane permeability to Na⁺ and raises the threshold, such as GABA, glycine and the endorphins.
- Meninges
- The three protective membranes covering the brain and spinal cord: dura matter, arachnoid matter and pia matter.
- Cerebrospinal fluid (CSF)
- The fluid between the arachnoid and pia matter that cushions the brain from shock.
- Cerebrum
- The largest part of the human brain, divided into two cerebral hemispheres, each with frontal, parietal, temporal and occipital lobes.
- Thalamus
- A part of the forebrain that receives all sensory impulses (except smell) and channels them to the limbic system and cortex.
- Limbic system
- A complex set of structures on both sides of the thalamus, just under the cerebrum, including the hypothalamus, amygdala and hippocampus.
- Hypothalamus
- The part of the limbic system on the ventral side of the thalamus that maintains homeostasis and controls the pituitary gland.
- Amygdalae
- Two almond-shaped masses of neurons that control feelings and emotions such as love, hate, anger, fear and rage.
- Hippocampus
- A structure of the limbic system that converts short-term memory into long-term memory.
- Cerebellum
- The part of the hindbrain that controls equilibrium and the coordination of muscles.
- Pons
- A part of the hindbrain that acts as a bridge between the cerebellum, medulla and cerebrum and controls the rate and pattern of heartbeat and breathing.
- Medulla
- A part of the hindbrain that controls automatic functions such as heartbeat, blood pressure, respiration and swallowing.
- Grey matter
- Neuron cell bodies and non-myelinated parts of fibres; inside the spinal cord (H-shaped) and the outer cortex of the brain.
- White matter
- Bundles of myelinated fibres; at the periphery of the spinal cord and inside the brain.
- Cranial nerves
- The 12 pairs of nerves of the peripheral nervous system that arise from the brain.
- Spinal nerves
- The 31 pairs of mixed nerves of the peripheral nervous system that arise from the spinal cord.
- Somatic nervous system
- The cranial and spinal nerve fibres that connect the CNS to the skin and skeletal muscles; involved in conscious activities.
- Autonomic nervous system
- The fibres that connect the CNS to the visceral organs; concerned with unconscious activities and divided into sympathetic and parasympathetic divisions.
- Sympathetic division
- The part of the autonomic system, from T1 to L2 of the spinal cord, that prepares the body for "fight or flight" in an emergency.
- Parasympathetic division
- The part of the autonomic system (a few cranial nerves including the vagus, and sacral nerves) that controls functions at rest and reverses the changes of the sympathetic division.
- Nociceptors
- Pain receptors: free nerve endings in the epidermis that respond to chemicals from damaged tissue or excess heat or pressure.
- Narcotic drugs
- Drugs that interact with normal nervous activity and diminish the perception of pain by binding to painkilling sites in the brain.
- Drug addiction
- A dependence on an illegal drug or a medication that most people cannot quit on their own.
- Drug tolerance
- A diminished response to a drug that occurs when the drug is used repeatedly and the body adapts to it, for example caffeine and nicotine.
- Analgesics
- Painkillers: medicines that reduce or numb pain through various mechanisms affecting the nervous system.
- Stroke
- A vascular disorder caused by rupture of small cerebral arteries, with sudden loss of function in one region of the brain.
- Meningitis
- Inflammation of the meninges caused by a bacterial or viral infection.
- Electroencephalography (EEG)
- A technique that records the electrical activity of the cerebral cortex with electrodes on the scalp, giving an electroencephalogram (brain waves).
- CT scan
- Computed tomography: an X-ray procedure combining many X-ray images with a computer to give cross-sectional and 3-D images of the body.
- MRI
- Magnetic resonance imaging: a radiology technique using magnetism, radio waves and a computer to produce detailed images of body structures.
Multiple choice questionsp. 113–114
- Aeffector organ to the spinal cord
- Breceptor cells to the effector organ
- Creceptor cells to the spinal cordAnswer
- Dspinal cord to the effector organ
A sensory (afferent) neuron carries impulses from receptor cells to the spinal cord, where the message is processed.
Option A reverses this path, and option D describes a motor neuron, which carries impulses away from the CNS. Option B skips the spinal cord, which every reflex arc passes through.
- A\ce{Na+} into the axon and \ce{K+} out of the axonAnswer
- B\ce{Na+} into the axon to bond with \ce{K+}
- C\ce{K+} into the axon and \ce{Na+} out of the axon
- D\ce{Na+} and \ce{K+} within the axon towards the axon terminal
During depolarization the voltage-regulated sodium gates open and \ce{Na+} diffuses into the axon, so the inside becomes positive. Potassium leaves the axon later, during repolarization.
Option C reverses the two movements. Option B is wrong because ions do not combine inside the axon, and option D describes movement along the fibre, not the ion change that causes depolarization.
- Ainhibition of acetylcholine
- Binhibition of cholinesterase
- Cmuscle contraction
- Dmuscle paralysisAnswer
Acetylcholine crosses the neuromuscular junction and binds receptors on the muscle membrane. If the receptors are blocked, the muscle membrane cannot depolarize, so the muscle cannot contract: it is paralysed.
Option A is wrong because blocking receptors does not stop acetylcholine being released. Option B would prolong contraction, since cholinesterase breaks acetylcholine down. Option C is the opposite of the result.
- Aaxon and dendrite
- Bsense organ and muscle effectorAnswer
- Cventral horn and dorsal horn
- Dmotor neuron and sensory neuron
A reflex arc starts at a receptor (a sense organ) and ends at an effector (a muscle or gland). The impulse passes through the sensory neuron, interneuron and motor neuron in between.
The other options name structures inside the path (axon, dendrite, horns of the grey matter, neurons), not its two ends.
- Aa nerve impulse is an all or none phenomenon
- Bthe nerves contain myelinated fibresAnswer
- Cthere is a high concentration of \ce{Na+} ions inside the axons
- Dthere is a potential difference across the axon membranes
In myelinated fibres the myelin sheath insulates the axon, so the impulse jumps from one node of Ranvier to the next (saltatory conduction). This is much faster than conduction along an unmyelinated fibre, and myelinated fibres conduct up to about 120 m per second.
Option A is true but does not explain speed. Option D is present in every neuron. Option C is wrong because \ce{Na+} is more concentrated outside the axon, not inside.
- Aon the nuclear membrane
- Bat nodes of Ranvier
- Con the postsynaptic membraneAnswer
- Din the myelin sheath
Neurotransmitter receptors are protein molecules on the post-synaptic membrane. The transmitter released from the presynaptic knob diffuses across the cleft and binds to them.
Nodes of Ranvier are gaps in the myelin sheath where the action potential is regenerated, not sites of receptors.
- Aglial cell
- Bmeninges
- CneuronAnswer
- Dcerebrospinal fluid
The neuron is the basic structural and functional unit of the nervous system. Each neuron receives, conducts and transmits impulses.
Glial cells support neurons, the meninges protect the brain and spinal cord, and cerebrospinal fluid cushions it. None of these conducts impulses.
- APia mater, arachnoid mater, durometerAnswer
- BPericardium, myocardium, endocardium
- CDurometer, pia mater, arachnoid mater
- DDurometer, arachnoid mater, pia mater
From the inside outwards the meninges are pia mater (next to the nervous tissue), arachnoid mater (the middle membrane) and dura mater (next to the skull or vertebrae). Option A gives this order.
Option B lists layers of the heart. Options C and D put the dura mater (printed as durometer) on the inside, which is the wrong order.
Note. The book prints durometer for dura mater in options A, C and D. Option A is correct with dura mater.
- ASchwann cells
- Bsynaptic cleft
- Csynaptic knobs
- Dsynaptic vesiclesAnswer
The neurotransmitter is stored in synaptic vesicles, which are membranous sacs inside the synaptic knob. When an impulse arrives, the vesicles fuse with the membrane and release the transmitter into the cleft.
The synaptic knob holds the vesicles but is the structure around them, and the cleft is where the transmitter goes after release. Schwann cells make the myelin sheath and have no part in storing transmitter.
- A\ce{K+} ions from intracellular to extracellular fluid
- B\ce{K+} ions from extracellular to intracellular fluid
- C\ce{Na+} ions from intracellular to extracellular fluid
- D\ce{Na+} ions from extracellular to intracellular fluidAnswer
The action potential is produced when voltage-regulated sodium gates open and \ce{Na+} ions flow in from the outside fluid down their concentration gradient. The inside becomes positive, and the wave moves along the membrane.
Option C reverses the direction of sodium movement. Options A and B involve potassium, which leaves the axon during repolarization and does not start the impulse.
Note. Misprint: the book numbers two questions 9. This is the second of them (the action potential question).
- Amyelination
- Bconductivity
- CirritabilityAnswer
- Dneurotransmission
Irritability is the ability of a neuron to respond to a stimulus that is strong enough (above threshold) and so start a nerve impulse.
Conductivity is the ability to carry an impulse once it has started, myelination is an insulating sheath, and neurotransmission is the transfer across a synapse.
- Ahypothalamus
- BcerebellumAnswer
- Ccorpus callosum
- Dspinal cord
The hindbrain consists of the cerebellum, the medulla oblongata and the pons. The cerebellum is therefore one of its parts.
The hypothalamus is part of the forebrain, the corpus callosum is a band of axons joining the two cerebral hemispheres, and the spinal cord is outside the brain.
- Aregulation of body temperatureAnswer
- Bdecision making
- Cco-ordination during locomotion
- Dshort-term memory
The hypothalamus maintains homeostasis. It contains centres that regulate body temperature, hunger, thirst, sleep and water balance.
Decision making is a function of the cerebrum, co-ordination of movement belongs to the cerebellum, and short-term memory is converted to long-term memory by the hippocampus.
- ACNS to muscles
- BCNS to receptors
- Creceptors to CNSAnswer
- Deffector organs to CNS
Afferent neurons are the sensory neurons. They carry impulses from receptors towards the central nervous system.
Motor (efferent) neurons carry impulses from the CNS to muscles and glands, so option A describes the opposite direction. Effector organs do not send impulses to the CNS.
- AVII
- BVIII
- CIX
- DXAnswer
Cranial nerve X is the vagus nerve. It is part of the parasympathetic division and helps control heart rate, and it also acts on the digestive organs.
Nerve VII is the facial nerve, VIII the auditory (vestibulocochlear) nerve, and IX the glossopharyngeal nerve, which serves taste and swallowing.
- Aprotein
- Bribosome
- CRNAAnswer
- DDNA
Nissl's granules are groups of ribosomes and rough endoplasmic reticulum in the cytoplasm of the cell body. Their ribosomes are built from RNA, so the granules are rich in RNA and protein synthesis takes place on them.
Ribosomes (option B) are the particles that make up the granules rather than the material they are made of. DNA (option D) is in the nucleus, not in the granules.
Note. The usual key is RNA. Option B is partly true, because the granules are built from ribosomes, so a student may read it as a second answer. RNA is the material the question asks for.
- Aafferent neuronAnswer
- Befferent neuron
- Cboth
- Dnone
An afferent (sensory) neuron carries information from the peripheral nervous system to the central nervous system.
An efferent (motor) neuron carries information the other way, from the CNS to effectors. So the answer is not both, and not none.
- Athalamus
- Bcerebellum
- Cpons
- DhypothalamusAnswer
The hypothalamus contains the centres that regulate body temperature, hunger (urge of eating), thirst, sleep and water balance.
The thalamus relays sensory impulses, the cerebellum co-ordinates movement and balance, and the pons relays signals and helps regulate breathing.
- Abrain and spinal cordAnswer
- Bspinal nerves only
- Ccerebrum and the spinal column
- Dbrain stem and the cerebellum
The central nervous system is made of the brain and the spinal cord. It is the coordinating centre of the body.
Spinal nerves are part of the peripheral nervous system. The spinal column is bone, and the brain stem and cerebellum are only parts of the brain.
- AmedullaAnswer
- Bcerebrum
- Cpons
- Dcerebellum
The medulla oblongata controls automatic (involuntary) activities such as breathing, swallowing, heartbeat and blood pressure, and it contains the reflex centres for coughing and sneezing.
The cerebrum controls conscious and voluntary activity, the pons relays signals and sets the pattern of breathing, and the cerebellum co-ordinates movement.
- Anodes of Ranvier
- BmeningesAnswer
- Caxomembranes
- Dmyelin sheath
The meninges are three protective membranes (dura mater, arachnoid mater and pia mater) that cover the brain and the spinal cord.
Nodes of Ranvier are gaps in the myelin sheath of axons, and the myelin sheath wraps individual axons, not the brain. Axomembranes is not a membrane covering the CNS.
Short answer questionsp. 114–115
Neuron co-ordination lets the body detect a change, decide what to do and respond quickly, so that the body parts work together as one unit.
- Reception: receptors detect a stimulus inside or outside the body and change it into a nerve impulse.
- Processing: the CNS (brain and spinal cord) analyses the information and decides on a response.
- Response: impulses travel to muscles and glands, which contract or secrete, so the body reacts within a fraction of a second (for example, withdrawing a hand from a hot object).
Receptors are biological transducers. A transducer converts one form of energy into another, and a receptor cell converts the energy of a stimulus into an electrochemical nerve impulse in a sensory neuron.
- Conversion: light, heat, sound, pressure and chemicals are changed into electrical impulses that travel to the CNS.
- Sensitivity: each receptor responds to one kind of stimulus. Mechanoreceptors (Meissner's corpuscles, Merkel's disks, Pacinian corpuscles) respond to touch and pressure, thermoreceptors (Ruffini and Krause endings) to heat and cold, and nociceptors (free nerve endings) to pain.
- Arrangement: receptors are massed together in sense organs such as the eye and ear, or scattered in the skin and internal organs.
A reflex arc is the path of the impulse during a reflex action. Its five fundamental parts, in the order the impulse travels, are:
- Receptors (sense organ) that detect the stimulus, for example the pain receptors in the skin.
- Sensory (afferent) neuron that carries the impulse from the receptor to the spinal cord.
- Interneuron (relay neuron) inside the spinal cord that passes the impulse on to the motor neuron.
- Motor (efferent) neuron that carries the impulse from the spinal cord to the effector.
- Effector (a muscle or a gland) that contracts or secretes to produce the response.
A neurotransmitter is a chemical messenger that carries the nerve impulse across a synapse, from the presynaptic neuron to the postsynaptic neuron or effector.
- Release: when an impulse reaches the synaptic knob, vesicles release the neurotransmitter into the synaptic cleft.
- Action: it diffuses across the cleft and binds to receptors on the postsynaptic membrane. Excitatory transmitters, such as acetylcholine, open sodium channels and start a new impulse. Inhibitory transmitters, such as GABA and glycine, make it harder for an impulse to start.
- Removal: enzymes break the neurotransmitter down (acetylcholine is hydrolysed by acetylcholinesterase), so the signal stops and the synapse is ready for the next impulse.
The brain and the spinal cord form the central nervous system, and they share several features.
- Both are the coordinating centre of the body. Together they receive information from the body and send out commands to the effectors.
- Both are hollow and contain cerebrospinal fluid. The brain has four ventricles and the spinal cord has a central canal, and both are bathed in cerebrospinal fluid that cushions them from shock.
- Both are covered by the three meninges (dura mater, arachnoid mater and pia mater), and both are protected by bone (the cranium and the vertebral column). Both also contain grey and white matter, arranged in opposite positions.
The limbic system is a complex set of structures lying on both sides of the thalamus, just under the cerebrum. It includes the hypothalamus, the amygdala, the hippocampus and several nearby areas.
- Hypothalamus: maintains homeostasis by controlling hunger, thirst, sleep, body temperature, water balance and blood pressure.
- Amygdala: controls feeling and emotions such as love, hate, anger and fear.
- Hippocampus: converts things in the short-term memory into long-term memories.
The dermis and epidermis of the skin contain the following sensory receptors.
| Receptor | Detects |
|---|---|
| Meissner's corpuscles | touch (numerous in the lips, fingertips, palm and soles) |
| Merkel's disks | touch |
| Pacinian corpuscles | pressure, deep in the fatty layer |
| Ruffini endings | heat |
| Krause end bulbs | cold |
| Free nerve endings (nociceptors) | pain |
Meissner's corpuscles and Merkel's disks are touch receptors, and pressure and touch are also called mechanoreceptors.
Narcotic drugs are agents that interact with the normal nervous activity. They reduce the perception of pain and alter the brain's chemistry.
- Binding: narcotics bind to the painkilling sites in the brain (opioid receptors). They copy the action of the natural painkilling chemicals and block pain signals.
- Effect: they diminish the perception of pain and cause a feeling of euphoria, while depressing the rate of breathing and circulation.
- Long-term use: with constant use the drugs build up in the brain and block the production of endorphins, the brain's natural painkillers. The body then depends on the drug and needs more of it to feel the same effect.
Alcohol withdrawal is the group of symptoms that appear when a person who has been drinking heavily suddenly stops. The common symptoms are:
- feeling of anxiety
- irritability
- depression
- headache
- hallucinations
Each difference is set out as a comparison table with the main points of difference, which is the form FBISE expects for a three-point answer.
| Feature | Thermoreceptors | Nociceptors |
|---|---|---|
| Stimulus | change in temperature (heat and cold) | tissue damage, excess heat or pressure, and chemicals from damaged tissue |
| Structure | encapsulated endings (Ruffini endings and Krause end bulbs) | free nerve endings with no capsule |
| Location | dermis of the skin | top of the skin (epidermis) and most tissues except the brain |
| Feature | Axoplasm | Axolemma |
|---|---|---|
| What it is | the cytoplasm inside an axon | the plasma membrane that encloses the axon |
| Contents or structure | fluid rich in potassium and negative organic ions | a lipid bilayer with ion gates and the sodium-potassium pump |
| Role in impulse | carries the ions that move during the impulse | its gates open and close, producing the action potential |
| Feature | Neuroglial cells | Schwann cells |
|---|---|---|
| Location | supporting cells of the nervous system (CNS and PNS) | only in the peripheral nervous system |
| Function | support, nourish and protect the neurons | wrap around axons to form the myelin sheath |
| Effect on impulse | no direct role in conduction | myelin speeds conduction by saltatory conduction |
| Feature | Sensory neuron | Motor neuron |
|---|---|---|
| Function | carries impulses from receptors to the CNS | carries impulses from the CNS to muscles and glands |
| Structure | unipolar, with its cell body in the dorsal root ganglion | multipolar, with its cell body in the spinal cord or brain cortex |
| Location | from sensory organs to the CNS | from the CNS to muscles and glands |
| Feature | Reflex action | Reflex arc |
|---|---|---|
| Meaning | an immediate, automatic and involuntary response to a stimulus | the path the nerve impulse follows during a reflex action |
| Parts | the response itself | receptor, sensory neuron, interneuron, motor neuron and effector |
| Example | withdrawing the hand from a hot object | pain receptor in the skin, through the spinal cord, to the arm muscle |
| Feature | Resting membrane potential | Active membrane potential |
|---|---|---|
| Charge across membrane | outside positive, inside negative (about -70\,\mathrm{mV}) | inside briefly positive (about +30 to +50\,\mathrm{mV}) |
| Ion movement | sodium-potassium pump active, sodium gates closed, potassium leaks out | voltage-regulated sodium gates open and sodium flows in |
| Duration | maintained until the membrane is stimulated | brief, about 1 millisecond, and it spreads along the axon |
| Feature | Depolarization | Repolarization |
|---|---|---|
| Potential change | moves from -70\,\mathrm{mV} towards zero and to +50\,\mathrm{mV} | returns from the peak towards the resting value |
| Ions involved | sodium gates open and \ce{Na+} enters | potassium gates open and \ce{K+} leaves |
| Phase of the spike | rising phase | falling phase |
| Feature | Repolarization | Hyperpolarization |
|---|---|---|
| Potential | returns to the resting value of about -70\,\mathrm{mV} | goes slightly beyond the resting value, to a more negative level |
| Cause | sodium gates close and potassium gates open | potassium gates close more slowly than sodium gates |
| Result | the membrane returns to its resting state | the pump then restores the resting potential |
| Feature | Refractory period | Absolute refractory period |
|---|---|---|
| Meaning | the whole recovery time (about 4 milliseconds) after an action potential | the early part of the recovery in which no new impulse can be started, however strong the stimulus |
| Ionic state | the original ion distribution is restored by the sodium-potassium pump | sodium gates are closed and cannot be opened again at once |
| Effect | limits a neuron to about 250 impulses per second | keeps each impulse separate and makes conduction one way |
| Feature | Presynaptic neuron | Postsynaptic neuron |
|---|---|---|
| Role | carries the impulse towards the synapse | receives the impulse after it crosses the synapse |
| Part at the synapse | axon terminal (synaptic knob) with synaptic vesicles | membrane with receptors for the neurotransmitter |
| Action | releases the neurotransmitter | binds the neurotransmitter and generates an impulse or potential |
| Feature | Axon | Dendrite |
|---|---|---|
| Shape and size | long and thick with a constant diameter, may be myelinated and may be branched | short and thin, highly branched and tapering |
| Direction of impulse | conducts the impulse away from the cell body | conducts the impulse towards the cell body |
| Function | carries the impulse to the synaptic terminals | receives stimuli from receptors or other neurons |
| Feature | Synaptic knob | Synaptic vesicles |
|---|---|---|
| What it is | the enlarged end of an axon branch (presynaptic terminal) | small membranous sacs found inside the knob |
| Contents | contains the vesicles; the impulse arrives here | store the neurotransmitter |
| Function | the site where the transmitter is released | fuse with the membrane and release the transmitter into the cleft |
| Feature | Pons | Medulla oblongata |
|---|---|---|
| Position | in the hindbrain, above the medulla and in front of the cerebellum | the lowest part of the brain, continuous with the spinal cord |
| Main role | a bridge linking the cerebellum, medulla and cerebrum; sets the rate and pattern of breathing and heartbeat | controls automatic functions such as heartbeat, blood pressure, breathing and swallowing |
| Type of control | relays and regulates | vital reflex centre |
| Feature | White matter | Grey matter |
|---|---|---|
| Made of | bundles of myelinated nerve fibres | neuron cell bodies, dendrites and nonmyelinated fibres |
| Position in the spinal cord | outside (periphery) | inside, in the shape of an H or a butterfly |
| Position in the brain | inside, below the cortex | outer layer (cerebral cortex) |
| Feature | Myelinated nerve fibre | Nonmyelinated nerve fibre |
|---|---|---|
| Sheath | has a myelin sheath with nodes of Ranvier | has no myelin sheath and no nodes of Ranvier |
| Speed of impulse | very fast, up to about 120 m per second, by saltatory conduction | very slow |
| Colour in fresh tissue | white | grey |
| Feature | Cranial nerves | Spinal nerves |
|---|---|---|
| Origin | arise from the brain | arise from the spinal cord |
| Number | 12 pairs, numbered I to XII in Roman numerals | 31 pairs |
| Area served | head, neck and torso (sense organs and facial muscles) | trunk, arms and legs through the dorsal and ventral rami |
| Feature | Drug addiction | Drug tolerance |
|---|---|---|
| Meaning | dependence on a drug, which the user finds hard to stop | a diminished response to a drug after repeated use, so higher doses are needed |
| Example | heroin and nicotine | caffeine and nicotine |
| Result | compulsive use and withdrawal symptoms when the drug is stopped | the same effect needs more of the drug; it can occur without addiction |
| Feature | Somatic nervous system | Autonomic nervous system |
|---|---|---|
| Control | voluntary, conscious activity | involuntary activity of organs, glands and blood vessels |
| Nerves | cranial and spinal nerves to the skin and skeletal muscles | fibres to the heart, stomach, intestines and glands |
| Divisions | none | sympathetic (fight or flight) and parasympathetic (rest or digest) |
Extensive answer questionsp. 115
The human nervous system is organized into two main parts, the central nervous system (CNS) and the peripheral nervous system (PNS). Together they receive stimuli, process the information and produce responses.
Central nervous system
- Brain: receives and processes sensory information, initiates responses, stores memories, and generates thoughts and emotions.
- Spinal cord: conducts signals to and from the brain and controls reflex actions.
Peripheral nervous system
- Sensory (afferent) neurons: carry impulses from sensory receptors to the CNS.
- Motor (efferent) neurons: carry impulses from the CNS to muscles and glands (effectors).
- Somatic nervous system: cranial and spinal nerves that connect the CNS to the skin and skeletal muscles; it controls voluntary activity.
- Autonomic nervous system: nerves that connect the CNS to the heart, stomach, intestines and glands; it controls involuntary activity.
Working of the nervous system
- Reception: receptors detect a stimulus and send an impulse along a sensory neuron.
- Processing: the brain or spinal cord analyses the information and decides on a response.
- Response: an impulse travels along a motor neuron to a muscle or gland, which contracts or secretes.
A neuron, the basic structural and functional unit of the nervous system, has three basic components: a cell body, dendrites and an axon. Although neurons vary in size and shape, they share this basic plan.
Cell body
- Contains granular cytoplasm and one large, centrally placed nucleus with a prominent nucleolus.
- Contains Golgi apparatus, mitochondria and other organelles.
- Nissl's granules: groups of ribosomes and rough endoplasmic reticulum that carry out protein synthesis.
Dendrites and axon compared
| Feature | Dendrite | Axon |
|---|---|---|
| Length and thickness | short and thin | long and thick, with a constant diameter |
| Branching | often highly branched, tapering to the tips | may be branched or unbranched |
| Direction of impulse | towards the cell body | away from the cell body, to the axon terminals |
| Covering | not myelinated | may be covered by a myelin sheath made by Schwann cells |
| Ends in | receives input from axon terminals of other neurons | axon terminals (synaptic knobs) that form synapses |
Myelin sheath and nodes of Ranvier
In many axons Schwann cells wrap around the axon to form a myelin sheath. The gaps between successive Schwann cells are the nodes of Ranvier. The myelin sheath speeds up the impulse because the impulse jumps from node to node.
Neurons are classified by their function into sensory, interneurons and motor neurons. They form a pathway in which an impulse passes from a receptor, through the CNS, to an effector.
Sensory neurons (afferent neurons)
- Structure: unipolar; the cell body lies in the dorsal root ganglion outside the CNS; a long dendrite reaches the receptor and the axon enters the CNS.
- Function: carry impulses from sensory receptors to the CNS. Many are myelinated, which speeds the impulse.
Interneurons (relay or association neurons)
- Structure: multipolar; the cell body lies entirely within the brain and spinal cord; the dendrites are highly branched.
- Function: connect sensory and motor neurons, process information and take part in reflexes. Local interneurons have short axons, and relay interneurons have long axons that link regions of the brain.
Motor neurons (efferent neurons)
- Structure: multipolar; the cell body lies in the spinal cord (lower motor neurons) or the cerebral cortex (upper motor neurons); the axon is long and often myelinated.
- Function: carry impulses from the CNS to muscles and glands, producing movement or secretion.
Comparison
| Neuron | Structure | Location | Function |
|---|---|---|---|
| Sensory | unipolar, long axon | from sensory organs to the CNS | carries impulses to the CNS |
| Interneuron | multipolar, short axon, branched dendrites | inside the brain and spinal cord | relays impulses between sensory and motor neurons |
| Motor | multipolar, long axon | from the CNS to muscles and glands | carries impulses from the CNS to effectors |
A synapse is the junction between the axon terminal of one neuron (the presynaptic neuron) and the dendrite or cell body of another neuron (the postsynaptic neuron). The two neurons do not touch: a gap called the synaptic cleft separates them, so the impulse is carried across by a chemical messenger, the neurotransmitter.
Steps
- An action potential arrives at the synaptic knob. Calcium channels open, and \ce{Ca^2+} ions flow into the knob because their concentration outside is higher.
- The rise in calcium makes the synaptic vesicles move towards the presynaptic membrane and fuse with it.
- The vesicles release their neurotransmitter molecules into the synaptic cleft (exocytosis).
- The neurotransmitter diffuses across the cleft, which takes about one millisecond, and binds to receptor molecules on the postsynaptic membrane.
- Binding opens channels, and \ce{Na+} ions diffuse into the postsynaptic neuron. The membrane depolarizes, producing an excitatory postsynaptic potential (EPSP). If the threshold is reached, a new action potential starts.
- The neurotransmitter is broken down by enzymes (acetylcholine by acetylcholinesterase), so the signal stops. The products are removed and the synapse is ready for the next impulse.
Neurotransmitters are classified by their effect on the postsynaptic neuron. Excitatory neurotransmitters increase the permeability of the membrane to sodium ions and so trigger an impulse. Inhibitory neurotransmitters decrease that permeability, which raises the threshold and makes an impulse less likely.
Excitatory neurotransmitters
- Acetylcholine: excitatory in the peripheral nervous system, for example at the neuromuscular junction.
- Biogenic amines (amino acid derivatives), important in the central nervous system: epinephrine and norepinephrine (noradrenaline), which increase the heartbeat rate during stress; serotonin and dopamine, which affect sleep, mood, attention and learning.
Inhibitory neurotransmitters
- Gamma-aminobutyric acid (GABA) and glycine: amino acids that lower the chance that an impulse will pass to the next neuron.
- Endorphins: peptides that act both as neurotransmitters and as hormones and reduce the perception of pain.
| Class | Effect on the membrane | Examples | Main role |
|---|---|---|---|
| Excitatory | increases sodium permeability; triggers an impulse | acetylcholine, epinephrine, norepinephrine, serotonin, dopamine | transmit impulses; heartbeat in stress; mood and sleep |
| Inhibitory | decreases sodium permeability; raises the threshold | GABA, glycine, endorphins | reduce transmission; reduce pain perception |
The brain is the largest part of the central nervous system. It is divided into three parts: the forebrain, the midbrain and the hindbrain. It is a hollow structure with four cavities called ventricles, and it is protected by the cranium and the three meninges.
Forebrain
- Cerebrum: the largest part, divided into two cerebral hemispheres joined by the corpus callosum. Each hemisphere has four lobes (frontal, parietal, temporal and occipital). The cortex has sensory, association and motor areas, and it controls reasoning, judgement, memory, thoughts and dreams.
- Thalamus: lies below the cerebrum and receives all sensory impulses except smell. It channels them to the limbic system and to the cortex for interpretation.
- Hypothalamus: lies on the ventral side of the thalamus and keeps the body in homeostasis. It contains centres for hunger, thirst, sleep, body temperature, water balance and blood pressure, and it controls the pituitary gland.
- Limbic system: structures on both sides of the thalamus, including the amygdala (feelings and emotions) and the hippocampus (turns short-term memory into long-term memory).
Midbrain
The midbrain is small in humans. It is a relay station for tracts passing between the cerebrum and the spinal cord or cerebellum, and it contains the reticular formation, which connects the hindbrain with the forebrain.
Hindbrain
- Cerebellum: controls equilibrium, body position and the co-ordination of muscles for complex movements such as walking and running. It is also involved in storing memories of learned movements.
- Pons: a bridge between the cerebellum, medulla and cerebrum. It regulates the rate and pattern of breathing and heartbeat.
- Medulla oblongata: controls automatic functions such as heartbeat, blood pressure, breathing and swallowing.
Summary
| Region | Main parts | Main functions |
|---|---|---|
| Forebrain | cerebrum, thalamus, hypothalamus, limbic system | thought, memory, reasoning, sensory relay, homeostasis, emotions |
| Midbrain | relay tracts and reticular formation | relays between cerebrum, spinal cord and cerebellum |
| Hindbrain | cerebellum, pons, medulla oblongata | co-ordination, balance, breathing and heartbeat |
The spinal cord is the link between the brain and the body. It extends from the medulla to the level of the lumbar vertebrae and is enclosed in the vertebral column. It is covered by the three meninges, and cerebrospinal fluid surrounds it.
Transverse section
- White matter (outside): bundles of myelinated nerve fibres that carry impulses up and down the cord.
- Grey matter (inside): neuron cell bodies, dendrites and nonmyelinated fibres, in the shape of an H or a butterfly. The dorsal horn receives sensory fibres and the ventral horn contains motor neuron cell bodies.
- Central canal: a tiny cavity in the centre, filled with cerebrospinal fluid.
- Dorsal root: carries sensory fibres into the cord. It has a dorsal root ganglion just outside the cord, which contains the sensory cell bodies.
- Ventral root: carries motor fibres out of the cord.
- Spinal nerve: formed where the dorsal and ventral roots join. Each spinal nerve is mixed, carrying sensory, motor and autonomic fibres.
Arrangement compared with the brain
The arrangement of grey and white matter in the brain is the opposite of that in the spinal cord. In the brain the grey matter forms the outer cortex and the white matter lies inside.
Function
The spinal cord conducts signals between the body and the brain and controls reflex actions, such as withdrawing a hand from a hot object, without the brain.
The peripheral nervous system can be divided into the somatic and the autonomic nervous systems. Both carry impulses between the CNS and the rest of the body, but they differ in what they control and in whether the control is conscious.
Somatic nervous system
- Made of cranial and spinal nerve fibres that connect the CNS to the skin and the skeletal muscles.
- Involved in conscious, voluntary activities such as walking, writing and speaking.
Autonomic nervous system
- Made of fibres that connect the CNS to the visceral organs, such as the heart, stomach, intestines and various glands.
- Concerned with unconscious, involuntary activities that work automatically.
Sympathetic and parasympathetic divisions
| Feature | Sympathetic division | Parasympathetic division |
|---|---|---|
| State | emergency: prepares the body for fight or flight | rest: returns body functions to normal, digests food |
| Origin in the spinal cord | first thoracic to second lumbar segments | cranial nerves (including the vagus) and nerves from the sacral region |
| Effect | increases heart rate and activity | reverses the sympathetic changes once the danger is over |
Comparison of the two systems
| Feature | Somatic | Autonomic |
|---|---|---|
| Control | voluntary, conscious | involuntary, unconscious |
| Target | skin and skeletal muscles | heart, stomach, intestines, glands |
| Nerves | cranial and spinal nerves | fibres of cranial and spinal nerves, in two divisions |
Narcotics are substances that diminish the perception of pain. They bind to painkilling sites in the brain and interact with the normal activity of the nervous system. Common narcotic drugs are heroin, cannabis, nicotine, alcohol and inhalants.
Common narcotic drugs
| Drug | Source or nature | Effects on the nervous system | Harmful effects |
|---|---|---|---|
| Heroin | narcotic that gives euphoria and pain relief | euphoria and relief of pain | nausea, vomiting, respiratory and circulatory depression leading to death |
| Cannabis | dried flowering tops, leaves and stem of the Indian hemp plant Cannabis sativa (marijuana, hashish) | mild euphoria; changes in vision and judgement | hallucinations, anxiety and depression |
| Nicotine | alkaloid derived from tobacco; spreads quickly to all organs | stimulates postsynaptic receptors (like acetylcholine); increases skeletal muscle activity | increases heartbeat and blood pressure; cancer, insomnia, cardiovascular disease, mouth ulcers |
| Alcohol | depressant | slows nervous communication; impairs vision, judgement and alertness | long-term drinking damages the nervous system, liver and pancreas |
| Inhalants | volatile organic chemicals (glue, aerosols, hair spray, ether) | rapid euphoria followed by depression of the central nervous system | hallucinations or death |
How narcotics act
- They bind to the painkilling sites in the brain and block pain signals.
- With constant use they build up in the brain and block the production of endorphins, the brain's natural painkillers.
- Depressants (such as alcohol) slow down the functioning of the central nervous system, while stimulants increase heart rate and concentration.
- The regions most affected are the brain stem, the limbic system and the cerebral cortex.
Addiction and tolerance
Drug addiction is dependence on a drug, which the user finds hard to stop. Drug tolerance is a diminished response to a drug after repeated use, so higher doses are needed for the same effect. Alcohol withdrawal, which occurs when drinking is suddenly stopped, causes anxiety, irritability, depression, headache and hallucinations.
Cause
A stroke occurs when a small cerebral artery ruptures, or when the blood supply to part of the brain is cut off, so that the tissue dies (cerebral infarction). Risk factors include hypertension, cigarette smoking, diabetes mellitus, high alcohol intake, thrombosis, blood disorders, blood embolism and cocaine abuse.
Symptoms
- sudden loss of function in one region of the brain
- weakness or paralysis of the arm, leg or face on the side of the body opposite the damage
- aphasia (inability to express thoughts through words) may be present
Treatment
Medical treatment aims to prevent further attacks and strokes. Anticoagulants and an antiplatelet drug such as aspirin are given, blood pressure is managed, and nursing care is essential.
Cause
Headache is pain anywhere in the head or neck. The brain tissue itself has no pain receptors, so the pain comes from disturbance of the pain-sensitive structures around the brain. Primary headaches (for example migraine and tension headache) occur on their own. Secondary headaches are caused by an underlying problem such as bleeding in the brain, a tumour or meningitis.
Symptoms
- pain in the head or neck, which varies with the type of headache
Treatment
Analgesic drugs relieve the pain of any kind of headache. A secondary headache is treated through its underlying cause.
Cause
Meningitis is inflammation of the meninges, usually caused by a bacterial or viral infection of the meninges.
Symptoms
- stiffness in the neck
- headache and fever
- in severe cases, paralysis, coma or death
Treatment
Viral meningitis has no specific treatment. Bacterial meningitis is treated with antibiotics and steroids.
Cause
A tumour is an abnormal mass of neuroglial cells produced by uncontrolled cell division. It is caused by a mutation, which may occur at any age in the brain or spinal cord.
Symptoms
- headaches and severe nerve pain
- paralysis and seizures
- coma and death in severe cases
- the symptoms vary with the location of the tumour
Treatment
Surgical removal of the tumour.
Cause
Alzheimer disease is a slowly progressive degenerative disease of the brain. It is caused by genetic predisposition, so it tends to run in families. Onset occurs mainly in older people, but it is not particularly associated with ageing.
Symptoms
- short-term memory loss, which is the most prominent symptom
- later, impaired reasoning, planning and language
Treatment
There is no effective treatment for this disease.
Principle: neurons in the cerebral cortex continuously generate electrical activity. Electrodes attached to precise points on the scalp pick up this activity. It is amplified and recorded as an electroencephalogram, whose patterns are called brain waves.
Brain waves
- Alpha: medium-frequency waves during wakefulness, when the person is relaxed.
- Beta: irregular, low-amplitude waves when the person is very alert and attentive.
- Theta: irregular waves as the person becomes drowsy, at the transition between wakefulness and sleep, with sleep spindles (bursts of 12 to 14 Hz) and K complexes in the sleeping stage.
- Delta: high-amplitude waves in the deep stage of sleep, which occupy 20 to 50 percent of the time.
Principle: a CT scanner combines many X-ray images taken from different angles. An X-ray source and detectors rotate around the body on a motorized platform, and a fan-shaped X-ray beam passes through each slice of the body. A computer uses the many images to produce cross-sectional views and, when needed, three-dimensional images of organs and structures.
A CT scan defines normal and abnormal structures in the body and helps guide the placement of instruments or treatment. The images are very detailed, but the radiation dose can be about 100 times that of a standard X-ray.
Principle: the MRI scanner is a tube surrounded by a giant circular magnet. The patient lies on a moveable bed that is inserted into the magnet and is exposed to a strong magnetic field and a beam of radio waves. The receiver detects the signals returned by the body, and a computer processes them to produce an image.
The image and resolution produced by MRI are very detailed, and MRI can detect tiny changes in the structures within the body.
Pain medicines (analgesics, or painkillers) work at different points along the pain pathway. Pain begins when a tissue is damaged. The damaged tissue releases chemicals that stimulate pain receptors, the impulse travels along a sensory neuron into the spinal cord, and from there to the thalamus and the cerebral cortex, where pain is felt.
Main groups of pain medicines
| Medicine | How it works | Effect |
|---|---|---|
| NSAIDs (non-steroidal anti-inflammatory drugs) | inhibit the enzyme cyclooxygenase (COX), so fewer prostaglandins are made at the injury | reduce pain, swelling and fever |
| Acetaminophen (paracetamol) | acts on the pain centre of the brain and inhibits COX in the brain | reduces the perception of pain without an anti-inflammatory effect |
| Opioids (narcotics) | bind to opioid receptors in the brain and spinal cord, block pain signals and raise the threshold for pain | dulls pain and produces euphoria; can cause addiction |
| Local anaesthetics | block sodium channels in nerve cells, so the signal cannot travel from the injury to the brain | numbs a small area, used in dental work and minor surgery |
| Antidepressants and anticonvulsants | modulate neurotransmitters involved in pain perception, such as serotonin and norepinephrine | treat chronic nerve pain |
| Corticosteroids | inhibit the production of inflammatory chemicals and suppress the immune response | reduce swelling and inflammation, which in turn reduces pain |
| Other medicines | numb a localized area; some relax muscles | numbs the local area and relaxes muscles |
Addiction to pain medicines
Opioids dull pain and also produce a sense of euphoria, and they cause neurons to release dopamine, which creates feelings of pleasure. With tolerance, a person needs higher doses, so the risk of opioid use disorder increases. For this reason physicians reduce the length and strength of opioid treatment.
FBISE 2026 questions
Questions from the FBISE HSSC-II 2026 (1st Annual) papers that belong to this unit, answered the way an examiner expects.
- AProvides balance and equilibrium in voluntary movements
- BIs a relay center between Hind and forebrain
- CConnects the right and the left HemisphereAnswer
- DControls auditory and visual reflexes
The cerebrum is divided into two cerebral hemispheres, and the corpus callosum is the band of axons that joins them, so each hemisphere can pass information to the other. Option A describes the cerebellum (balance and coordination of voluntary movement), option B the thalamus (a relay centre), and option D the midbrain, so they are the tempting wrong answers.
Identification (1 mark). The structure is a synapse, the junction where the swollen end of one neuron (the synaptic knob) meets the next cell, here a banded (striated) cell, as at a neuromuscular junction. The two cells are not in contact: a gap, the synaptic cleft, separates them, and the impulse crosses it as a chemical, the neurotransmitter.
Labelling A to D (2 marks)
| Label | Part | Description |
|---|---|---|
| A | Synaptic knob (with synaptic vesicles) | Rounded swelling at the end of the axon of the presynaptic neuron; the vesicles in it hold the neurotransmitter |
| B | Axon of the presynaptic neuron | Carries the impulse to the knob |
| C | Postsynaptic cell (muscle fibre or next neuron) | Receives the message; its membrane carries receptors and ion channels |
| D | Synaptic cleft with the presynaptic membrane | Narrow gap between the knob and the postsynaptic cell |
The graph is the action potential of a neuron: the potential rises from the resting level (−70 mV) past the threshold (−55 mV) to about +40 mV, then falls and dips below the resting level before returning to it.
| Label | Process | What happens |
|---|---|---|
| X | Depolarization (rising limb) | The threshold stimulus opens the voltage-regulated Na⁺ gates. Na⁺ diffuses into the axon, so the inside changes from negative to positive (about −70 mV up to +40 mV). |
| Y | Repolarization (falling limb) | The Na⁺ gates close and the K⁺ gates open. K⁺ diffuses out, so the inside becomes negative again and the potential falls back towards −70 mV. |
| Z | Hyperpolarization (undershoot) | The K⁺ gates close slightly later than the Na⁺ gates, so extra K⁺ leaves and the potential goes a little below −70 mV. The sodium-potassium pump then restores the resting potential. |
a. Release of neurotransmitter at the synaptic knob (2 marks)
- An action potential reaches the synaptic knob and opens Ca²⁺ channels in the presynaptic membrane. Ca²⁺ is more concentrated outside, so it rushes in.
- The rise in Ca²⁺ inside the knob makes the synaptic vesicles move to the presynaptic membrane and fuse with it.
- The fused vesicles release the neurotransmitter into the synaptic cleft by exocytosis; the molecules diffuse across the cleft.
b. Effect on the postsynaptic membrane (1 mark)
The neurotransmitter binds to receptor molecules on the postsynaptic membrane. This opens ion channels, so Na⁺ diffuses in and the membrane depolarises towards the threshold (an excitatory postsynaptic potential, EPSP). If threshold is reached, an action potential starts in the postsynaptic neuron. The neurotransmitter is then broken down by enzymes (acetylcholine by acetylcholinesterase) so the membrane can reset.
Both are imaging tests that give detailed pictures of the inside of the body, but they work on different principles.
| Feature | CT scan | MRI |
|---|---|---|
| Principle | An X-ray procedure: a tomograph takes X-ray images at many angles round the body and a computer combines them | Uses magnetism, radio waves and a computer: the patient lies in a tube surrounded by a giant circular magnet and is exposed to a strong magnetic field and a beam of radio waves |
| Image produced | Cross-sectional views (tomograms) and, if needed, three-dimensional images | Very detailed images with high resolution that can detect tiny changes of structure |
| Radiation | Needs a dose of radiation that can be 100 times that of a standard X-ray | Uses no X-rays; only magnetic field and radio waves |
- A3\ \ce{Na+} out and 2\ \ce{K+} inAnswer
- BEqual \ce{Na+}, \ce{K+} in and out
- C3\ \ce{Na+} in and 2\ \ce{K+} out
- D2\ \ce{Na+} in and 3\ \ce{K+} out
For every cycle the pump uses ATP to move three Na⁺ out of the neuron and two K⁺ in, both against their concentration gradients. Because more positive charge leaves than enters, the inside becomes more negative, which helps to set up the resting potential of −70 mV. Options C and D reverse the direction: Na⁺ is already about 10 times more concentrated outside, so moving it out is what needs energy.
Synapse (1 mark)
A synapse is the junction between the axon terminal of one neuron (presynaptic neuron) and the dendrite of another neuron (postsynaptic neuron), where information is passed from one neuron to the next. The neurons do not touch: a gap, the synaptic cleft, lies between them. The axon ends in rounded synaptic knobs containing synaptic vesicles full of neurotransmitter. The impulse crosses the cleft as a chemical, so it travels in one direction only.
Labelled diagram (2 marks)
Nerve impulse. A nerve impulse is information or a signal about a stimulus that is carried from receptors to the CNS and from the CNS to the effectors. In technical terms it is a wave of electrochemical changes (an action potential) travelling along the length of a neuron.
Generation in a neuron
- Resting state (polarised). The pump moves 3 Na⁺ out for 2 K⁺ in, K⁺ leaks out and negative organic ions stay inside, so the inside is negative: the resting potential is −70 mV.
- Stimulus. A threshold stimulus opens the voltage-regulated Na⁺ gates.
- Depolarization. Na⁺ diffuses in, the inside becomes positive (up to about +50 mV).
- Repolarization. The K⁺ gates open, K⁺ diffuses out and the inside becomes negative again.
- Recovery. The sodium-potassium pump restores the original ion distribution (refractory period, about 4 ms), ready for the next impulse. The change spreads to the next part of the axon, so the impulse travels along it.
Drug addiction (1.5 marks)
- Drugs are chemicals that interfere with the way neurons send, receive and process information. Some activate neurons because their structure mimics a natural neurotransmitter (for example nicotine stimulates postsynaptic receptors like acetylcholine).
- Narcotics bind to painkilling sites in the brain. With constant use they build up and block the production of endorphins, the brain's natural painkillers, so the person depends on the drug.
- The parts of the brain affected are the brain stem, limbic system and cerebral cortex. Depressants such as alcohol slow down the CNS; stimulants increase heart rate, concentration and breathing rate. Stopping suddenly causes withdrawal symptoms (anxiety, irritability, depression, headache, hallucinations).
Drug tolerance (1.5 marks)
- Tolerance is a diminished response to a drug: with repeated use the body adapts to its continued presence.
- The nervous system responds less to the same dose, so higher doses are needed to get the same alertness or effect (for example caffeine and nicotine).
- The person keeps taking more of the drug, and the harmful effects on the body continue (for nicotine: cardiovascular disease, insomnia, headache), so tolerance and addiction go together.
Exam focus
- Describe the mechanism of synaptic transmission and draw the labelled synapse (synaptic knob, vesicles, cleft, receptors, postsynaptic membrane). (long)Asked in 2026 three times: Set B Q.2 (v) (identify and label the junction), Set B Q.2 (vi) OR (release of neurotransmitter and its effect on the postsynaptic membrane) and Set D Q.2 (vi) (describe a synapse and draw it). Also book long question 4.Go to answer
- Explain how a nerve impulse is generated: resting potential, depolarization, repolarization, hyperpolarization. (long)Set D Q.2 (viii) (what is a nerve impulse and how is it generated) and Set B Q.2 (v) OR (identify X, Y, Z on the action potential graph). Book exercise MCQ 2 and 9b also test the ion movements.Go to answer
- Read and label the action potential graph: threshold, resting potential, rising limb, falling limb, undershoot. (short)Set B Q.2 (v) OR gave the graph and asked for X, Y and Z with a short description of each.Go to answer
- State what the sodium-potassium pump does (3 Na+ out, 2 K+ in) and how the resting potential of -70 mV is set up. (short)Set D MCQ 6 asked the pump ratio directly; the resting potential factors are a standard short question.Go to answer
- Drug addiction and tolerance and their effects on the nervous system (narcotics, endorphins, depressants and stimulants, caffeine, nicotine). (short)Set D Q.2 (xiii) OR asked to associate addiction and tolerance with nervous system functioning (1.5 + 1.5 marks). Book long question 9 covers narcotic drugs.Go to answer
- Describe the structure of a neuron and the three types of neuron with their functions. (long)Not asked as a paper question in 2026, but it is the base of the unit (book long questions 2 and 3) and the labelled neuron diagram is a likely draw-and-label.Go to answer
- Name the parts of the human brain and the function of each (corpus callosum, cerebellum, thalamus, hypothalamus). (short)Set B MCQ 5 (corpus callosum connects the two hemispheres). Book long question 6 and MCQs 11, 12 and 17 ask the same brain-part functions.Go to answer