Nervous Coordination (A Level Only)

Belajar sambil bermain

Jawab soal-soal ini untuk dapat energi, lalu memancing dan menjelajah. Tanpa akun.

Untuk pendidik: slide pelajaran, catatan ulasan siap pakai untuk Nervous Coordination (A Level Only) (Biology, AQA) — gunakan dalam pelajaranmu, atau jalankan topik sebagai aktivitas kelas interaktif yang dimainkan pembelajar sebagai permainan langsung.

Catatan pelajaran

Motor Neurone Structure

  • Nerve impulses are electrical signals that pass along neurones; a bundle of neurones is called a nerve.
  • Sensory neurones carry impulses from receptors to the CNS; relay neurones connect sensory and motor neurones within the CNS; motor neurones carry impulses from the CNS to effectors.
  • Motor neurones have a cell body at one end (within the CNS), a long axon, and axon terminal endings located within effectors.
  • Some motor neurones have a myelin sheath, a fatty substance made by Schwann cells that wrap around the axon.
  • The presence of myelin speeds up the conduction of nerve impulses.
  • The long axon allows impulses to be transmitted over long distances, and dendrites allow connections with other neurones.

Resting Potential

  • Neurones not actively transmitting impulses have a resting potential of about -70 mV across their cell surface membrane.
  • This means the inside of the axon is 70 mV more negative than the outside.
  • Resting potential is established and maintained by sodium-potassium pumps and the outward flow of potassium ions.
  • Sodium-potassium pumps use ATP to actively transport 3 Na⁺ out for every 2 K⁺ in, creating a larger concentration of positive ions outside the axon.
  • Potassium ions diffuse out of the axon by facilitated diffusion through open potassium ion channels; sodium ion channels are closed at this point.
  • The difference in permeability to sodium and potassium is called differential membrane permeability.
  • The open potassium channels involved in resting potential are not voltage-gated and should not be confused with voltage-gated potassium channels.

Action Potentials

  • When a neurone is stimulated, sodium ion channels open, sodium ions enter the axon, and the inside becomes less negative; this is depolarisation (the generator potential).
  • If the membrane potential reaches about -50 mV (the threshold potential), voltage-gated sodium ion channels open and more sodium ions enter.
  • Enough sodium ions enter for the membrane potential to reach about +30 mV; this is an action potential.
  • During repolarisation, voltage-gated sodium channels close and voltage-gated potassium channels open, allowing potassium ions to diffuse out.
  • Hyperpolarisation occurs when potassium ions continue to leave until the inside is more negative than resting potential; this is the refractory period.
  • The all-or-nothing principle: if threshold is not reached, no action potential occurs; if threshold is reached, an action potential of the same size (+30 mV) always occurs.
  • A stronger stimulus produces a higher frequency of action potentials; a weaker stimulus produces a lower frequency.
  • The refractory period ensures new action potentials are generated ahead of the original, so impulses travel in one direction, and keeps impulses as separate events.

Nerve Impulse Transmission

  • Action potentials occur at the point of stimulation and are transmitted along the axon as nerve impulses.
  • In non-myelinated neurones, sodium ions diffuse along the axon, depolarising the next section; voltage-gated sodium channels open if threshold is reached.
  • The impulse does not travel backwards because the membrane behind the action potential is in a hyperpolarised state.
  • In myelinated neurones, the myelin sheath stops diffusion of sodium and potassium ions, so depolarisation cannot occur in myelinated sections.
  • Sodium ions diffuse from one node of Ranvier to the next, setting up local currents and initiating action potentials at each node.
  • Action potentials appear to jump from node to node; this is saltatory conduction, which is much faster than in unmyelinated axons of the same diameter.

Speed of Impulse Conduction

  • The speed of impulse conduction depends on myelination, axon diameter, and temperature.
  • Myelinated neurones conduct impulses faster because depolarisation occurs only at the nodes of Ranvier, relying on diffusion of sodium ions (saltatory conduction).
  • In unmyelinated neurones, depolarisation must occur along the whole membrane, which is relatively slow.
  • Wider axons conduct impulses faster: larger diameter gives a higher volume of cytoplasm, reducing resistance to ion flow, and fewer ions leak across the membrane.
  • Higher temperatures increase the speed of conduction because molecules have more kinetic energy, so diffusion and respiration (providing ATP) are faster.
  • In mammals, stable body temperature limits the effect of environmental temperature; in reptiles, nerve impulse transmission is affected by external temperature.

Calculating Maximum Impulse Frequency

  • After an action potential, the axon enters a refractory period during which it cannot be stimulated again.
  • The duration of the refractory period determines the maximum frequency of impulse conduction.
  • Maximum frequency = time ÷ duration of the refractory period; for 1 second, it is 1 ÷ duration of the refractory period.
  • Units may be impulses sec⁻¹, action potentials sec⁻¹, or Hz; 1 Hz = one impulse per second.
  • Convert milliseconds to seconds before calculating (divide by 1000).
  • Example: a refractory period of 2.75 ms = 0.00275 s, so maximum frequency = 1 ÷ 0.00275 = 364 action potentials sec⁻¹.

Synapse Structure and Synaptic Transmission

  • Synapses are junctions between cells in the nervous system, consisting of a presynaptic cell, a postsynaptic cell, and the synaptic cleft between them.
  • The postsynaptic cell can be another neurone or an effector cell (e.g. a muscle cell).
  • Nerve signals cross synapses as neurotransmitters, which are released from vesicles, diffuse across the cleft, and bind to receptors on the postsynaptic cell.
  • At a cholinergic synapse, an action potential causes voltage-gated calcium channels to open and calcium ions to enter the presynaptic neurone.
  • Calcium ions cause vesicles containing acetylcholine (ACh) to fuse with the presynaptic membrane and release ACh into the synaptic cleft.
  • ACh diffuses across the cleft and binds to receptor proteins on the postsynaptic membrane, opening sodium ion channels and depolarising the postsynaptic membrane.
  • If threshold is reached, a new action potential is generated in the postsynaptic neurone.
  • Acetylcholinesterase hydrolyses ACh in the synaptic cleft; the products are absorbed by the presynaptic cell to produce more ACh.

Summation and Inhibitory Synapses

  • Synapses ensure unidirectional transmission because calcium channels and neurotransmitter vesicles are only in the presynaptic cell, and receptors are only on the postsynaptic membrane.
  • A single impulse may not release enough neurotransmitter to reach threshold; this allows the nervous system to filter out low-level stimuli.
  • Summation occurs when multiple impulses arrive together, increasing the chance of reaching threshold.
  • Temporal summation: rapid, repeated release of neurotransmitter from one neurone; neurotransmitter builds up until threshold is reached.
  • Spatial summation: multiple impulses arrive at the same time from several presynaptic cells; their combined neurotransmitter reaches threshold.
  • Excitatory synapses initiate a new action potential by causing an influx of positive ions.
  • Inhibitory synapses prevent a new action potential by causing hyperpolarisation, e.g. by opening potassium channels (K⁺ outflow) or chloride channels (Cl⁻ inflow).
  • A neurone may receive both excitatory and inhibitory input, allowing complex information processing.

Drugs and Synapses

  • Drugs can affect synaptic transmission by stimulating neurotransmitter release, providing chemicals to synthesise neurotransmitters, imitating neurotransmitters by binding to receptors, or preventing reuptake.
  • Dopamine agonists bind to dopamine receptors and produce the same effect as dopamine; dopamine precursors are converted into dopamine inside neurones.
  • These treatments are used in Parkinson's disease, where not enough dopamine is produced in specific parts of the brain.
  • Morphine mimics endorphins, binds to endorphin receptors, and stimulates dopamine release, leading to pain relief and pleasure.
  • Cocaine binds to dopamine transporter proteins on the presynaptic membrane, blocking reabsorption and causing dopamine to build up in the synapse, overstimulating the postsynaptic neurone.
  • Cannabinoids bind to receptors on presynaptic membranes of neuromuscular junctions, causing calcium ion channels to close, reducing neurotransmitter release and weakening muscle contraction.
  • MDMA stimulates the release of several neurotransmitters, most notably serotonin, altering mood.

Neuromuscular Junctions

  • Neuromuscular junctions are specialised synapses between a motor neurone (presynaptic cell) and a muscle cell (postsynaptic cell).
  • When an impulse arrives, calcium ion channels open, calcium ions enter the neurone, and vesicles of ACh fuse with the presynaptic membrane.
  • ACh diffuses across the cleft and binds to receptors on the sarcolemma, opening sodium ion channels and depolarising the muscle cell.
  • If threshold is reached, an action potential is generated and transmitted into the muscle cell via T-tubules.
  • This causes voltage-gated calcium channels in the sarcoplasmic reticulum to open, releasing calcium ions into the sarcoplasm and triggering muscle contraction.
  • Acetylcholinesterase breaks down ACh when stimulation ends, and the products are reabsorbed by the presynaptic cell.
  • Unlike cholinergic synapses, neuromuscular junctions have folded postsynaptic membranes (storing AChE), T-tubules, are always excitatory, and represent the end of a nerve pathway.

Slide

Sign up free to view the lesson slides

Step through every slide for this topic — plus flashcards and revision notes — with a free account.

Soal latihan

Pratinjau gratis — 8 dari 64 soal. Daftar untuk melihat semuanya.
  1. 1.Which type of neurone carries nerve impulses from receptors to the central nervous system (CNS)?

    Easy
    • ASensory neurone
    • BRelay neurone
    • CMotor neurone
    • DInterneuron
  2. 2.Which of the following correctly describes the resting potential of a neurone?

    Easy
    • AThe inside of the axon is 70 mV more negative than the outside
    • BThe inside of the axon is 70 mV more positive than the outside
    • CThe inside of the axon is 30 mV more positive than the outside
    • DThe inside of the axon is 30 mV more negative than the outside
  3. 3.Myelin is a fatty substance produced by Schwann cells that wraps around the axon.

    Easy

    True or false?

  4. 4.During an action potential, what is the threshold potential that must be reached for voltage-gated sodium ion channels to open?

    Medium
    • A-70 mV
    • B-50 mV
    • C+30 mV
    • D+40 mV
  5. 5.Which of the following is the correct sequence of events during an action potential?

    Easy
    • ADepolarisation → Repolarisation → Hyperpolarisation
    • BRepolarisation → Depolarisation → Hyperpolarisation
    • CHyperpolarisation → Depolarisation → Repolarisation
    • DDepolarisation → Hyperpolarisation → Repolarisation
  6. 6.During the transmission of an action potential along a non-myelinated axon, why does the nerve impulse not travel backwards?

    Medium
    • AThe membrane behind the action potential is hyperpolarised and cannot be stimulated
    • BSodium ions diffuse only forwards along the axon
    • CVoltage-gated sodium channels are permanently closed behind the action potential
    • DThe myelin sheath prevents backward transmission
  7. 7.Which of the following statements about the refractory period are true? (Select all that apply.)

    Medium
    • AIt ensures nerve impulses are transmitted in one direction
    • BIt allows nerve impulses to merge together
    • CIt is the time when the membrane is hyperpolarised
    • DIt limits the maximum frequency of action potentials
    • EIt occurs during depolarisation
  8. 8.Match each structure of a cholinergic synapse with its correct description.

    Medium
    • Presynaptic membrane
    • Synaptic cleft
    • Postsynaptic membrane
    • Vesicle
    • Membrane of the neurone that carries the impulse towards the synapse
    • Gap between the two cells
    • Membrane of the cell that receives the signal
    • Structure containing neurotransmitter

Unlock all 64 questions & more

Buat akun gratis untuk melihat setiap soal, slide, kartu flash, dan catatan ulasan topik ini.

Soal ujian lampau

Latihan soal ujian lampau untuk topik ini segera hadir.
Segera hadir