B15 Nervous Coordination and Muscles Flashcards

1
Q

How do we maintain resting potential of a neurone

A

Using sodium-potassium ion pumps.

They actively transport 3 Na+ out the neurone

They actively transport 2 K+ into the neurone.

Ensures more positive ions outside the neurone than inside

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2
Q

What is the resting potential of neurones

A

-70mV

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3
Q

4 steps in order of how an Action Potential is formed

A
  1. Depolarisation
  2. Repolarisation
  3. Hyperpolarisation
  4. Restoring of the resting potential via Na-K ion pump
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4
Q

When a neurone is stimulated, the membrane becomes

A

depolarised

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5
Q

What is the threshold potential

A

-55mV

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6
Q

Depolarisation process

A

If the threshold potential of -55mV is met:
Na+ channels open
K+ channels closed
So Na+ diffuse into the neurone via facilitated diffusion.
This decreases the potential difference across the membrane until it reaches a voltage of around +30mV

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7
Q

Repolarisation process

A

Na+ channels close
K+ channels open
K+ ions diffuse down their concentration gradients out of the neurone which reestablishes the charge difference in the membrane.

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8
Q

Hyperpolarisation

A

Few too many K+ ions diffuse out as the K+ channels are too slow to close.
So the charge difference exceeds the resting potential

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9
Q

Restoring of RP

A

The action of the sodium-potassium ion pump restores the balance of Na and K on either side of the membrane

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10
Q

Diagram of an action potential. Time against voltage

A

Search it up

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11
Q

How is an AP stimulated across the neuronea

A

A wave of depolarisation occurs along the neurone because sodium ions diffuse into the neurone sideways

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12
Q

What is the refractory period

A

Time immediately after an action potential has been stimulated where a neurone cannot be stimulated so an AP cant occur.

This is because ion channels are recovering

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13
Q

Why is a refractory period good

A

Ensures AP’s don’t overlap/ prevents neurones from being overstimulated

Ensures that AP’s are unidirectionals

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14
Q

Different sized stimuli result in …

A

Different frequencies of action potentials

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15
Q

Factors affecting the speed of an action potential

A

Myelination
Axon diameter
Temperature

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16
Q

How does myelination affect the conduction velocity of an AP

A

Myelin Sheath acts as an electrical insulator which prevents ion movement across the membrane

Depolarisation can only occur at the nodes of Ranvier where the voltage-gated sodium ion channels are concentrated

So action potentials ‘jump’ from node to node - saltatory conduction

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17
Q

What is saltatory conduction

A

When action potentials jump from node to node in myelinated neurones

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18
Q

Why does axon diameter affect the speed of an AP on a neurone

A

A bigger axon, AP travels quicker because there is less resistance to the flow of ions in the neurone

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19
Q

How does temperature affect the conduction velocity of an action potential

A

ions have a greater kinetic energy so diffuse faster and depolarisation can occur at a faster rate

ofc till optimum temp where channel proteins will denature and stuff

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20
Q

Synaptic Transmission process

A
  1. Action potential reaches the end of the presynaptic neurone.
  2. This triggers the opening of voltage-gated Calcium ion channels so Ca2+ enter the presynaptic neurone via facilitated diffusion
  3. Influx of calcium ions triggers the movement of vesicles towards the presynaptic membrane
  4. Vesicles fuse with membrane and release neurotransmitters via exocytosis
  5. NTs diffuse across the synaptic cleft and are detected by receptors on the postsynaptic neurone
  6. This triggers the opening of Na+ ion channels so sodium ions move into the postsynaptic neurone which stimulates depolarisation and therefore an AP is stimulated on the postsynaptic neurone.
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21
Q

What 2 things allow APs to travel unidirectionally

A
  1. refractory period
  2. receptors are found on the postsynaptic neurone
22
Q

What are cholinergic synapses

A

Synapses that use acetylcholine as the neurotransmitter

23
Q

What is acetylcholine broken down by

A

acetylcholinesterase

24
Q

How does acetylcholinesterase break down acetylcholine

A

into acetate and choline

products are reabsorbed into the presynaptic neurone to synthesise the neurotransmitter

25
Q

What are excitatory NTs

A

they trigger an AP in postsynaptic neurone

26
Q

What are inhibitory NTs

A

they prevent an AP from occuring

e.g. by opening K+ channels in postsynaptic neurone so instead of stimulating depolarisation, it stimulates more hyperpolarisation

27
Q

What is spatial summation

A

lots of presynaptic neurones converging to 1 single postsynaptic neurone

28
Q

What is temporal summation

A

1 single neurone fires an AP in quick succession repeatedly which releases small amounts of NTs into the synaptic cleft which all combined produces enough of an effect to stimulate an AP

29
Q

What are neuromuscular junctions in between

A

a motor neurone and a muscle cell

30
Q

What neurotransmitter do neuromuscular junctions use

A

acetylcholine

31
Q

Differences between neuromuscular junctions and a normal synapse

A

postsynaptic neurone is folded into clefts which stores the enzyme acetylcholinesterase
acts as an excitatory NT
has a high number of receptors on postsynaptic neurone

32
Q

What is skeletal muscle used in

A

any physical movement

33
Q

how can the muscles work

A

in antagonistic pairs so when 1 muscle contracts the other relaxes

e.g. when arm relaxes, the bicep (flexors) relaxes but the tricep (extensors) contracts

34
Q

The structure of skeletal muscles

A

bone > tendon > muscle > bundle of muscle fibres > muscle fibre > myofibril > sarcomeres

35
Q

What is a transverse tubule

A

when the sarcolemma folds into the sarcoplasm

36
Q

what does the sarcoplasmic reticulum do

A

stores calcium ions for muscle contraction

37
Q

what are the 2 types of myofilaments which make up myofibrils

A

actin and myosin

38
Q

myosin is the ___ filament and appears as the ____ / _ band

A

thick
dark
A

39
Q

actin is the ____ filament and appears as a ____/ _ band

A

thin
light
I

40
Q

Structure of sarcomere

A

search it up but basically
A band is middle dark section
I band is on either side of A band
Z line is at the end of the sarcomere
H-zone is the central region of the A band only containing myosin
M line is the centre line of the sarcomere

41
Q

Myosin myofilament structure

A

They have head groups which can bind to actin and ATP
Their heads are globular and hinged allowing them to move back and forth

42
Q

Under resting conditions, what blocks the actin-myosin binding site

A

tropomyosin ( sphere-like thing ) and troponin ( string )

43
Q

What happens when an AP arrives at a muscle fibre

A
  1. Wave of depolarisation passes along the sarcolemma and down the T-tubules
  2. This stimulates the sarcoplasmic reticulum to release the calcium ions
  3. The calcium ions bind to troponin, which causes it to change shape and pull tropomyosin out of the actin-myosin binding site so an actin-myosin cross-bridge can form
  4. Release of calcium ions also activates ATPase, which catalyses the hydrolysis of ATP into ADP + Pi.
  5. The energy released from this is used by the myosin head to move backwards, which pulls the actin filament closer towards it.
  6. ATP hydrolysis also provides energy to break the actin-myosin cross bridge.
  7. This allows myosin to reattach to a binding site further along the actin. This process is repeated and results in shortened sarcomeres and muscle contraction
44
Q

What happens when the muscle stops being stimulated

A

Calcium ions move back into the sarcoplasmic reitculum via active transport.
Troponin molecules reform their OG shape so tropomyosin is pushed back into the actin-myosin binding site

45
Q

What happens to the diff parts of sarcomeres during muscle contraction

A

A band stays the same length
I band shortens
Z lines become closer
H zone decrease in width

46
Q

What 3 ways generates ATP in muscle contraction

A

Aerobic respiration
- oxidative phosphorylation
Anaerobic respiration
-glycolysis
Phosphocreatine

47
Q

How does phosphocreatine work

A

Phosphocreatine phosphorylates ADP which releases ATP and creatine (removed via kidneys)

it is anaerobic and alactic

48
Q

Where is phosphocreatine stored

A

muscle cells

49
Q

When is phosphocreatine useed

A

very short bursts of vigorous exercise

50
Q

Slow twitch muscle fibres

A

contract for long periods of time without getting tired

most of the energy is supplied from aerobic respiration

51
Q

fast twitch muscle fibres

A

fatigue easy

get their energy from anaerobic respiration

used for short bursts of speed

52
Q

why do slow twitch fibres have a reddish appearance

A

due to high presence of myoglobin which is a protein which stores oxygen