(15) Nervous coordination Flashcards

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1
Q

why are neurone cell membranes polarised at rest

A

in resting state the outside of the membrane is positively charged compared to the inside as there are more positive ions in the outside than inside. polarised means there is a voltage / potential diff across it

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2
Q

what is the voltage across the membrane when it’s at rest (resting potential)

A

-70mV

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3
Q

how is the resting potential created and maintained

A

sodium potassium pumps move sodium ions out of the neurone but membrane isn’t permeable to sodium ions so they can’t move back in
creates a sodium ion electrochemical gradient because there are more positive sodium ions outside than inside (positively charged)
potassium ions can move in and out

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4
Q

how do neurone cell membranes become depolarised when stimulated

A

stimulus triggers sodium ion channels to open, membrane becomes more permeable, sodium ions diffuse in making inside of neurone less negative.
if P.D reaches -55mV more sodium channels open (depolarisation)
at +30mV sodium ion channels close and K ion channels open so K diffuses out (repolarisation) membrane returns to resting potential

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5
Q

what is hyperpolarisation

A

K ion channels are slow to close so theres a slight overshoot where too many K diffuse out and the P.D becomes more negative than resting potential (-70mV)

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6
Q

why can’t the neurone cell membrane be excited again straight away after an action potential

A

because the ion channels are recovering and can’t be made to open (refractory period)

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7
Q

what is a wave of depolarisation

A

when an action potential happens some of the sodium ions diffuse sideways causing Na ion channels in the next region of the neurone to open and Na diffuses into that part causing wave of depolarisation

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8
Q

what 3 things are as a result of the refractory period

A

1) action potentials don’t overlap but pass as separate impulses
2) theres a limit to teh freq at which nerve impulses can be transmitted
3) action potentials are unidirectional (only travel in one direction)

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9
Q

what does it mean by the all or nothing nature of an action potential

A
  1. action potential with the same change in voltage will always fire after the threshold is reached regardless of the stimulus
  2. action potential wont fire unless the threshold is reached
  3. bigger stimulus wont cause a bigger action potential only cause them to fire at a higher frequency
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10
Q

why are axons with larger diameters advantageous

A

action potentials are conducted quicker as theres less resistance to the flow of ions so depolarisation reaches other parts of the neurone cell membrane quicker

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11
Q

how is a higher temperature advantageous

A

speed of conduction increases with higher temp because ions start to diffuse faster. only up to 40c though as after that the proteins begin to denature

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12
Q

what are the benefits of myelination

A

myelin sheath is made of schwann cells which have nodes of ranvier where the sodium ion channels are concentrated. impulse jumps from node to node (saltatory conduction) which is really fast

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13
Q

how do impulses travel along non myelinated neurones

A

impulse travels as a wave along the whole length of the axon membrane so you get depolarisation along the whole length of the membrane (slower than saltatory conduction)

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14
Q

how do impulses jump between nodes

A

neurones cytoplasm conducts enough electrical charge to depolarise the next node so impulse can jump

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15
Q

what happens when an action potential reaches the end of a neurone

A

neurotransmitters are released into the synaptic cleft and diffuse across to the postsynaptic membrane where it binds to specific receptors

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16
Q

what makes impulses unidirectional

A

receptors for neurotransmitters are only on the postsynaptic membrane

17
Q

how do excitatory neurotransmitters work

A

depolarise the postsynaptic membrane making it fire an action potential if the threshold is reached

18
Q

how do inhibitory neurotransmitters work

A

hyperpolarise the postsynaptic membrane (making PD more negative) preventing it from firing an action potential

19
Q

what is summation

A

the effect of neurotransmitter released from many neurones is added together

20
Q

what is spatial summation

A

many neurones connect to one neurone (small amount of neurotransmitter from each neurone is added together to reach the threshold in the postsynaptic neurone and trigger an action potential)

21
Q

when can spatial summation lead to no action potential

A

if more inhibitory neurotransmitters are released than excitatory

22
Q

what is temporal summation

A

2 or more nerve impulses arrive in quick succession from the same presynaptic neurone making an action potential more likely because more neurotransmitter is released

23
Q

what is a neuromuscular junction

A

synapse between a motor neurone and a muscle cell

24
Q

what are agonists

A

drugs that are the same shapes as neurotransmitters so they mimic their action at receptors so more receptors are activated

25
Q

what are antagonists

A

drugs that block receptors so they can’t be activated by neurotransmitters so fewer receptors are activated

26
Q

what are inhibitory drugs

A

inhibitory: inhibit the enzymes that break down neurotransmitters so there are more neurotransmitters to bind to receptors or some drugs inhibit the release of neurotransmitters from the presynaptic neurone

27
Q

what are stimulatory drugs

A

stimulate the release of neurotransmitters from presynaptic neurone so more receptors are activated

28
Q

what is skeletal muscle made up of

A

muscle fibres and sarcolemma that folds in and sticks into the sarcoplasm to help spread electrical impulses throughout the sarcoplasm
sarcoplasm reticulum stores and releases calcium ions needed for muscle contraction
lots of mitochondria
multinucleate

29
Q

what are myofibrils

A
long cylindrical organelles made of protein specialised for contraction. 
contain thick (myosin) and thin (actin) myofilaments that move past each other to make muscles contract
30
Q

what is the sliding filament theory

A

myosin and actin filaments slide over each other to make the sarcomeres contract. the simultaneous contraction of lots of sarcomeres means the myofibrils and muscle fibres contract as the muscle fibre relaxes the sarcomere returns to its original length

31
Q

adaptations of myosin filaments

A

globular heads that are hinged so they can move back and forth. each myosin head has a binding site for actin and a binding site for ATP

32
Q

adaptations of actin filaments

A

binding sites for myosin heads (actin-myosin binding sites)

tropomyosin (protein) found between actin filaments helps myofilaments move past each other

33
Q

what is the function of tropomyosin

A

in resting unstimulated muscle the actin myosin binding site is blocked by tropomyosin so myofilaments cant slide past each other because the myosin heads can’t bind to the actin-myosin binding sites

34
Q

what is the ATP-phosphocreatine system (PCr)

A

ATP is made by phosphorylating ADP (adding a phosphate group taken from PCr)
PCr is stored inside cells and the ATP-PCr system generates ATP quickly- used for short bursts of vigorous exercise eg a tennis serve
anaerobic and alactic

35
Q

what are the properties of slow twitch muscle fibres

A

1) contract slowly
2) used for posture eg in back
3) endurance activities
4) work for a long time without getting tired
5) energy released slowly by aerobic respiration (lots of mitochondria and blood vessels to supply oxygen)
6) reddish as rich in myoglobin

36
Q

what are the properties of fast twitch muscle fibres

A

1) contract very quickly
2) used for fast movement eg in eyes and legs
3) good for short bursts of speed and power
4) get tired very easily
5) energys released through anaerobic respiration using glycogen (few mitochondria or blood vessels)
6) whitish in colour as not much myoglobin