How is a nerve impulse generated and propagated, and how is it transmitted across a synapse?
5.1.3 Neuronal communication: the structure of a neurone; the establishment of the resting potential by the sodium-potassium pump; the generation of an action potential by voltage-gated channels (depolarisation and repolarisation); the all-or-nothing principle and the refractory period; saltatory conduction in myelinated neurones; and synaptic transmission by acetylcholine at a cholinergic synapse.
A focused answer to the OCR H420 5.1.3 dot point on neuronal communication. Covers neurone structure, the resting potential, the action potential and its ionic basis, the all-or-nothing principle and refractory period, saltatory conduction, and synaptic transmission by acetylcholine.
Reviewed by: AI editorial process; not yet individually human-reviewed
Have a quick question? Jump to the Q&A page
Jump to a section
What this dot point is asking
OCR wants you to describe the structure of a neurone, explain the resting potential, explain the generation of an action potential through voltage-gated channels (depolarisation and repolarisation), explain the all-or-nothing principle and the refractory period, explain saltatory conduction, and describe synaptic transmission at a cholinergic synapse.
The answer
Neurone structure
A neurone carries electrical impulses. A motor neurone has a cell body with dendrites (receive impulses), a long axon (carries the impulse), and an axon terminal. Many neurones are wrapped in a myelin sheath of Schwann cells, with gaps called nodes of Ranvier; myelin acts as an electrical insulator.
The resting potential
At rest the inside of the axon is negative relative to the outside (about ), the resting potential. It is maintained by:
- the sodium-potassium pump, which actively pumps 3 sodium ions out for every 2 potassium ions in (using ATP);
- the membrane being more permeable to potassium than to sodium (potassium leaks back out).
The action potential
A stimulus changes the membrane potential. If it reaches the threshold (about ), an action potential fires:
- Depolarisation. Voltage-gated sodium channels open and sodium ions diffuse in, making the inside positive (about ).
- Repolarisation. The sodium channels close and voltage-gated potassium channels open; potassium ions diffuse out, returning the inside to negative.
- Hyperpolarisation. The potential briefly overshoots below the resting value before the sodium-potassium pump restores the resting potential.
The impulse propagates because depolarisation at one point triggers the channels at the next point (local currents).
All-or-nothing and the refractory period
- The all-or-nothing principle: an action potential only fires if the stimulus reaches threshold, and it is always the same size regardless of how strong the stimulus is. A stronger stimulus produces a higher frequency of impulses, not bigger ones.
- The refractory period is the short time after an action potential when the sodium channels are recovering and another impulse cannot fire. It ensures impulses are discrete (do not merge), travel in one direction, and limits the frequency.
Saltatory conduction
In a myelinated neurone, the myelin insulates the axon so depolarisation can only happen at the nodes of Ranvier. The action potential therefore jumps from node to node (saltatory conduction), which is much faster than the continuous conduction in an unmyelinated axon.
Synaptic transmission
At a cholinergic synapse (using acetylcholine):
- The action potential reaches the presynaptic membrane and opens voltage-gated calcium channels; calcium ions diffuse in.
- Vesicles of acetylcholine fuse with the presynaptic membrane and release it into the synaptic cleft by exocytosis.
- Acetylcholine diffuses across and binds to receptors on the postsynaptic membrane, opening sodium channels so the postsynaptic membrane depolarises; if threshold is reached a new action potential fires.
- Acetylcholinesterase breaks acetylcholine down so the response stops, and the products are reabsorbed and recycled.
Synapses ensure one-way transmission (only the presynaptic neurone has vesicles), and allow summation (adding stimuli) and integration of signals.
Examples in context
Example 1. Multiple sclerosis. In MS the myelin sheath is damaged, so saltatory conduction is disrupted and impulses travel slowly or fail, causing muscle weakness and numbness, a clear demonstration of myelin's role.
Example 2. Nerve agents and insecticides. Organophosphates inhibit acetylcholinesterase, so acetylcholine is not broken down and the postsynaptic neurone is continuously stimulated, causing uncontrolled muscle contraction, which shows why the enzyme is essential.
Try this
Q1. Explain how the sodium-potassium pump helps maintain the resting potential. [2 marks]
- Cue. It actively pumps 3 sodium ions out for every 2 potassium ions in (using ATP), so the inside becomes negative relative to the outside.
Q2. Explain why saltatory conduction is faster than conduction in an unmyelinated axon. [2 marks]
- Cue. Myelin insulates the axon, so depolarisation only occurs at the nodes of Ranvier and the impulse jumps from node to node rather than depolarising the whole membrane.
Q3. Name the enzyme that breaks down acetylcholine in the synaptic cleft. [1 mark]
- Cue. Acetylcholinesterase.
Exam-style practice questions
Practice questions written in the style of OCR exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.
OCR H420/01 20186 marksDescribe how an action potential is generated and then how the resting potential is restored at a point on an axon membrane.Show worked answer →
Sequence the ion movements through the voltage-gated channels.
At rest the inside of the axon is negative (about -70 mV), maintained by the sodium-potassium pump (3 sodium ions out for every 2 potassium ions in) and the membrane being more permeable to potassium.
Depolarisation: a stimulus opens some voltage-gated sodium channels; if the threshold (about -55 mV) is reached, many sodium channels open and sodium ions diffuse in, making the inside positive (about +40 mV).
Repolarisation: the sodium channels close and voltage-gated potassium channels open, so potassium ions diffuse out, returning the inside to negative. There is a brief hyperpolarisation before the sodium-potassium pump restores the resting potential.
Markers reward the resting potential maintained by the pump, threshold reached, sodium in for depolarisation, potassium out for repolarisation, and the pump restoring rest.
OCR H420/01 20225 marksDescribe how a nerve impulse is transmitted across a cholinergic synapse.Show worked answer →
Take it from arrival of the impulse to breakdown of the transmitter.
The action potential arrives at the presynaptic membrane and opens voltage-gated calcium channels, so calcium ions diffuse in. This causes vesicles of acetylcholine to move to and fuse with the presynaptic membrane, releasing acetylcholine into the synaptic cleft by exocytosis.
Acetylcholine diffuses across the cleft and binds to receptors on the postsynaptic membrane, opening sodium channels so sodium ions enter and depolarise the postsynaptic neurone; if threshold is reached, a new action potential is generated.
Acetylcholinesterase then breaks acetylcholine down (into choline and ethanoic acid) so the response stops and the products are recycled. Markers reward calcium entry, vesicle fusion and release, diffusion and receptor binding, depolarisation, and breakdown by acetylcholinesterase.
Related dot points
- 5.1.4 Hormonal communication: the principles of hormonal coordination and the contrast with nervous coordination; the structure and function of the adrenal glands and pancreas; the control of blood glucose concentration by insulin and glucagon (glycogenesis, glycogenolysis and gluconeogenesis); the second messenger model of adrenaline and glucagon; and the causes of type 1 and type 2 diabetes.
A focused answer to the OCR H420 5.1.4 dot point on hormonal communication. Covers hormonal versus nervous coordination, the adrenal glands and pancreas, the control of blood glucose by insulin and glucagon, the second messenger model, and the causes of type 1 and type 2 diabetes.
- 5.1.2 Homeostasis and excretion: the principles of homeostasis and negative feedback; the role of the liver in deamination and detoxification; the structure of the nephron and the processes of ultrafiltration and selective reabsorption; and osmoregulation by ADH acting on the collecting duct.
A focused answer to the OCR H420 5.1.2 dot point on homeostasis and the kidney. Covers negative feedback, the liver's role in deamination and detoxification, the nephron, ultrafiltration and selective reabsorption, and osmoregulation by ADH acting on the collecting duct.
- 5.1.5 Plant and animal responses: tropisms and the role of auxin (IAA) in phototropism; the structure and function of the mammalian nervous system (central and peripheral, voluntary and autonomic), the reflex arc and the fight-or-flight response; and the structure and the sliding filament mechanism of skeletal muscle contraction.
A focused answer to the OCR H420 5.1.5 dot point on plant and animal responses. Covers tropisms and the role of auxin in phototropism, the organisation of the mammalian nervous system, the reflex arc and fight-or-flight, and the sliding filament mechanism of muscle contraction.
- 3.1.2 Transport in animals: the structure of the mammalian heart and the events of the cardiac cycle (atrial systole, ventricular systole and diastole), the pressure and volume changes that open and close the valves, and the myogenic control of heart rate by the SAN, AVN, bundle of His and Purkyne tissue, including the interpretation of electrocardiograms (ECGs).
A focused answer to the OCR H420 3.1.2 dot point on the mammalian heart. Covers the heart's structure, the three stages of the cardiac cycle, how pressure changes open and close the valves, myogenic control by the SAN, AVN, bundle of His and Purkyne tissue, and how to read an ECG.
- 5.2.2 Respiration: the four stages of aerobic respiration (glycolysis, the link reaction, the Krebs cycle and oxidative phosphorylation); the role of decarboxylation, dehydrogenation, reduced NAD and FAD, the electron transport chain, chemiosmosis and ATP synthase; the synthesis of ATP and the role of oxygen as the final electron acceptor; and anaerobic respiration in animals (lactate) and in yeast (ethanol).
A focused answer to the OCR H420 5.2.2 dot point on respiration. Covers the four stages of aerobic respiration (glycolysis, the link reaction, the Krebs cycle and oxidative phosphorylation), chemiosmosis and ATP synthase, the role of oxygen, and anaerobic respiration producing lactate or ethanol.
Sources & how we know this
- OCR A Level Biology A (H420) Specification — OCR (2023)