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6.2Organisms Respond to Changes in their Environments (A Level only)

Nervous Coordination (A Level only) — AQA A Level Biology 7402 Revision Notes & Topical Questions

15 min read 23 parts Lesson 15 of 44 Unit quiz

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Neurone Structure, Resting Potential and Action Potentials — AQA A LEVEL BIOLOGY 7402 notes: Describe the structure of motor neurones and explain how resting potentials and action potentials are generated.Information is passed through the nervous system as nerve impulses, electri…

  • Depolarisation
  • Repolarisation
  • Hyperpolarisation
  • Worked example 1
  • Worked example 2
  • Worked example 3

Section 1 of 23Neurone structure

Information is passed through the nervous system as nerve impulses, electrical signals that travel along neurones.

1
A bundle of neurones is a nerve.
2
Different types of neurone carry impulses in different parts of the nervous system (sensory, relay and motor).
3
A motor neurone has a cell body, many dendrites, a long axon and a myelin sheath.
4
Structure links to function: the long axon carries impulses over long distances through the body; dendrites allow connections with other neurones; the myelin sheath speeds up conduction.

Section 2 of 23Resting potential

A neurone that is not transmitting an impulse has a difference in charge across its cell surface membrane, called the resting potential; the inside of the axon is negative relative to the outside, at around -70 mV.

Resting potential
It is established by sodium-potassium ion pumps,
  • which use ATP to pump 3 Na+ out and 2 K+ in, combined with the outward movement of potassium ions by facilitated diffusion through open channels.
This further increases the concentration of positive ions outside the axon, and a difference of -70 mV is achieved.

There are different types of ion channel in the axon membrane: some open and close depending on the voltage across the membrane, others do not. The open potassium channels that help set the resting potential are not voltage-dependent and should not be confused with the voltage-gated potassium channels involved in action potentials.

Section 3 of 23The action potential

In a resting axon the potential difference is about -70 mV. When a neurone is stimulated the membrane potential changes; if the stimulus is large enough to reach the threshold potential, an action potential results. Action potentials passed along neurones are nerve impulses.

Depolarisation
Depolarisation voltage-gated sodium ion channels open; sodium ions diffuse in down their electrochemical gradient and the inside becomes positive (about +40 mV).
Repolarisation
Repolarisation sodium channels close; voltage-gated potassium ion channels open and potassium ions diffuse out of the axon, down their concentration gradient,
  • and the inside of the membrane becomes more negative.
Hyperpolarisation
Hyperpolarisation the outward movement of potassium continues until the inside is more negative than the resting potential,
  • because the potassium channels stay open for longer than needed.
  • The hyperpolarised membrane is in the refractory period.
The voltage-gated potassium channels close and the sodium-potassium pumps restore the membrane to resting potential.

Section 4 of 23Coding intensity

Action potentials are all-or-nothing, so the strength of a stimulus is coded by frequency: a stronger stimulus gives a higher frequency of action potentials, a weaker stimulus gives a lower frequency. The refractory period ensures action potentials are separate and travel in one direction.

Section 5 of 23Worked examples

  1. Describe how the resting potential of an axon is established. [4]4 marks

  2. Describe the events of an action potential. [5]5 marks

  3. Explain how the brain can tell a strong stimulus from a weak one. [2]2 marks

  4. Explain the importance of the refractory period. [2]2 marks

Section 6 of 23Transmission in a non-myelinated neurone

Action potentials occur at the point of stimulation and are transmitted along the axon as nerve impulses.

Transmission in a non-myelinated neurone
In a non-myelinated neurone: (1) the initial influx of sodium ions increases sodium ion concentration inside the axon at that point; (2) sodium ions diffuse along the inside of the axon to the neighbouring resting region; (3) this depolarises the next section until threshold is reached, opening voltage-gated sodium channels and creating a new action potential; the process repeats along the whole length.
The refractory period behind the impulse ensures it moves in one direction.
Action potentials are transmitted along an axon because of the diffusion of sodium ions.

Section 7 of 23Myelinated neurones and saltatory conduction

Some neurones are surrounded by a fatty myelin sheath formed from Schwann cells.

Myelinated neurones and saltatory conduction
In sections of axon covered by myelin depolarisation cannot occur,
  • because myelin stops the diffusion of sodium and potassium ions across the membrane.
Sodium ions instead diffuse along the length of each Schwann cell, from one node of Ranvier to the next, initiating an action potential at each node.

Use language carefully

  • action potentials appear to jump between nodes of Ranvier, not between neurones.
  • Explain that action potentials occur only at the nodes, so the impulse appears to jump between them in saltatory conduction, which is faster.

Section 8 of 23Factors affecting the speed of conduction

FactorEffect and reason
MyelinationImpulses travel faster because they jump between nodes of Ranvier
Axon diameterWider axons conduct faster: larger volume of cytoplasm reduces resistance to ion flow, and fewer ions leak across the membrane, so the membrane potential is maintained more easily. Speed increases with diameter in all types of neurone, but higher speeds are reached in myelinated axons
TemperatureHigher temperature increases the rate of ion diffusion and the activity of carrier proteins, so impulses travel faster. Reptile body temperature fluctuates with their environment, so their nerve impulse speed is affected by external temperatures

Be prepared to apply this to unfamiliar contexts, for example impulse conduction data from different species.

Section 9 of 23Maximum frequency of impulses

After an action potential the axon recovers and is unresponsive; this is the refractory period, so there is a minimum time between action potentials.

1
Maximum frequency = 1 ÷ refractory period (in seconds).
2
Worked example: Figure 1 shows the refractory period labelled as 2.75 milliseconds.
3
Step 1: refractory period = 2.75 ms = 0.00275 s.
4
Step 2: 1 ÷ 0.00275 = about 364 action potentials per second.

Section 10 of 23Synapse structure

The junctions between cells in the nervous system are synapses. A synapse has a presynaptic cell (the neurone that carries a nerve impulse towards the synapse), the synaptic cleft, and the postsynaptic cell.

Section 11 of 23Worked examples

  1. Explain why impulses travel faster along myelinated axons. [3]3 marks

  2. Explain why a wide axon conducts impulses faster than a narrow one. [2]2 marks

  3. The refractory period is 2.75 ms. Calculate the maximum frequency of action potentials per second. [2]2 marks

  4. Suggest why impulse speed in a reptile varies with environment. [2]2 marks

Section 12 of 23Transmission across a cholinergic synapse

Synapses that use acetylcholine (ACh) are cholinergic synapses. Sequence: an action potential arrives at the presynaptic cell; voltage-gated calcium ion channels open and Ca2+ diffuse in; vesicles of ACh fuse with the presynaptic membrane and ACh is released by exocytosis into the synaptic cleft; ACh diffuses across and binds to receptors on the postsynaptic membrane; sodium ion channels open, Na+ enter and the membrane depolarises; if threshold is reached an action potential is generated; acetylcholinesterase then breaks down ACh so the response stops and the products are reabsorbed.

Use precise language

  • say acetylcholine is released from the presynaptic membrane into the synaptic cleft, not 'chemicals are released into the synapse'.
  • Impulses pass in one direction because neurotransmitter is released only from the presynaptic side and receptors are only on the postsynaptic membrane.

Section 13 of 23Summation

The first few impulses may not release enough neurotransmitter, but if stimulation continues the quantity in the cleft builds up until threshold is reached.

Temporal summation
In temporal summation multiple nerve impulses arrive at a presynaptic cell one after the other.
Spatial summation
In spatial summation impulses arrive at the same time from several different presynaptic cells and the neurotransmitter from them together reaches the threshold potential.

Section 14 of 23Inhibitory synapses

Some synapses are excitatory, causing depolarisation; others are inhibitory: they prevent a new action potential in the postsynaptic cell by causing hyperpolarisation, e.g. by opening chloride or potassium channels.

Inhibitory synapses
If an inhibitory synapse (Y) and an excitatory synapse (X) act together, the inhibitory synapse lowers the membrane potential, cancelling the effect of the excitatory synapse so the threshold is not reached and no action potential is generated.
You need not know a particular inhibitory synapse, only the principle, which may be applied to new scenarios.

Section 15 of 23Drugs and synapses

Drugs may affect synaptic transmission, for example by mimicking a neurotransmitter, blocking receptors, stopping reabsorption or breakdown of neurotransmitter, or changing its release. For example, when the postsynaptic neurone is overstimulated, producing feelings of pleasure. Cannabinoids bind to receptors on the presynaptic membranes of neuromuscular junctions, causing calcium ion channels to close; release of neurotransmitter is reduced, weakening muscle contraction.

Section 16 of 23Neuromuscular junctions

Neuromuscular junctions are specialised synapses at the junctions between neurones and muscles. The presynaptic cell is a motor neurone and the postsynaptic cell is a muscle fibre; the neurotransmitter is ACh.

Section 17 of 23Worked examples

  1. Describe the sequence of events at a cholinergic synapse. [5]5 marks

  2. Distinguish temporal and spatial summation. [2]2 marks

  3. Explain how an inhibitory synapse prevents an action potential in the postsynaptic neurone. [2]2 marks

  4. Explain how cannabinoids weaken muscle contraction. [3]3 marks

Section 18 of 23Events at a neuromuscular junction

A neuromuscular junction is a specialised cholinergic synapse between a motor neurone and a muscle fibre. Transmission follows the same early steps as other cholinergic synapses (action potential arrives, calcium ions enter, ACh is released into the cleft and binds to receptors on the postsynaptic membrane, the sarcolemma). Then:

The sarcolemma is depolarised, and if the threshold is reached an action potential is generated.
T-tubules
The action potential is transmitted into the interior of the muscle cell via deeply infolded regions of the sarcolemma called T-tubules; voltage-gated calcium ion channels in the membranes of the sarcoplasmic reticulum open.
Calcium ions diffuse out of the sarcoplasmic reticulum into the sarcoplasm surrounding the myofibrils.
The protein filaments inside the muscle cell move and muscle contraction occurs.
When stimulation ends the enzyme acetylcholinesterase (AChE) breaks down ACh and the products are reabsorbed by the presynaptic cell.

Section 19 of 23Comparing neuromuscular junctions and cholinergic synapses

As neuromuscular junctions are a type of synapse, they share many features with cholinergic synapses: in both, calcium ions trigger the release of neurotransmitter, acetylcholine is the neurotransmitter, and AChE removes it. Differences are summarised below.

FeatureCholinergic synapse (neurone to neurone)Neuromuscular junction
Postsynaptic cellAnother neuroneMuscle fibre (sarcolemma)
OutcomeMay be excitatory or inhibitoryAlways excitatory: leads to contraction
ResponseNew action potential in the postsynaptic neurone, if threshold reachedAction potential spreads along sarcolemma and down T-tubules
ReceptorsFewer, in a smaller membrane areaMore receptors on a folded postsynaptic membrane

Section 20 of 23Why the junction matters for movement

Because every action potential in the motor neurone releases enough ACh to depolarise the sarcolemma, a signal from the nervous system reliably leads to a muscle response.

Why the junction matters for movement
The rapid removal of ACh by acetylcholinesterase allows the muscle to relax and be stimulated again.
Drugs or toxins that block ACh receptors or inhibit acetylcholinesterase cause paralysis or prolonged contraction,
  • which shows how a neuromuscular junction links the nervous system and the muscular system.

Section 21 of 23Worked examples

  1. Describe how an action potential in a motor neurone leads to the release of calcium ions in a muscle fibre. [5]5 marks

  2. State the role of acetylcholinesterase at a neuromuscular junction. [2]2 marks

  3. State two similarities between a neuromuscular junction and a cholinergic synapse. [2]2 marks

Section 22 of 23Key terms

TermMeaning
Resting potentialThe potential difference across the membrane of a non-transmitting neurone, about -70 mV.
Action potentialA brief reversal of the membrane potential that travels along an axon as a nerve impulse.
DepolarisationMembrane potential becoming less negative as sodium ions enter.
RepolarisationReturn towards resting potential as potassium ions leave.
HyperpolarisationMembrane potential more negative than resting potential.
Refractory periodTime during which the axon cannot respond to another stimulus.
Sodium-potassium pumpCarrier that actively transports sodium out and potassium into the cell.
TermMeaning
Myelin sheathFatty insulating layer formed by Schwann cells around some axons.
Node of RanvierGap in the myelin sheath where action potentials occur.
Saltatory conductionImpulse appearing to jump between nodes of Ranvier.
SynapseJunction between two neurones or a neurone and an effector.
Presynaptic cellNeurone carrying an impulse towards a synapse.
Refractory periodRecovery time after an action potential when the axon is unresponsive.
TermMeaning
Cholinergic synapseA synapse that uses acetylcholine.
Synaptic cleftThe gap between presynaptic and postsynaptic membranes.
Temporal summationSummation of impulses arriving in rapid succession.
Spatial summationSummation of impulses arriving from several presynaptic neurones.
Inhibitory synapseSynapse that hyperpolarises the postsynaptic membrane and so prevents an action potential.
Neuromuscular junctionA specialised synapse between a motor neurone and a muscle.
AcetylcholinesteraseEnzyme that hydrolyses acetylcholine in the synaptic cleft.
TermMeaning
T-tubuleDeep infolding of the sarcolemma that carries action potentials into the muscle fibre.
SarcolemmaCell surface membrane of a muscle fibre.
Sarcoplasmic reticulumSpecialised endoplasmic reticulum storing calcium ions in muscle cells.
SarcoplasmCytoplasm of a muscle fibre.
AcetylcholinesteraseEnzyme that breaks down acetylcholine.

Section 23 of 23Exam technique

1
Confusing resting-potential potassium channels with voltage-gated potassium channels.
2
Saying a bigger stimulus makes a bigger action potential.
3
Describing depolarisation as the loss of sodium ions.
4
Forgetting that the pump is active transport requiring ATP.
1
Saying the action potential 'jumps' without saying it occurs only at nodes.
2
Saying it jumps between neurones.
3
Forgetting to convert milliseconds to seconds in frequency calculations.
4
Saying temperature affects only the pumps — it affects diffusion rates too.
1
Writing 'chemicals released into the synapse' instead of acetylcholine into the cleft.
2
Confusing temporal and spatial summation.
3
Saying inhibition happens by blocking release — it happens by hyperpolarising the postsynaptic membrane.
4
Forgetting that Ca2+ entry triggers release.
1
Saying T-tubules carry ACh — they carry the action potential.
2
Forgetting acetylcholinesterase removes ACh.
3
Saying calcium ions are released from the presynaptic neurone for contraction — contraction needs calcium from the sarcoplasmic reticulum.
4
Saying all synapses are excitatory.

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