Response - topic 7 Flashcards

(52 cards)

1
Q

What is an antagonistic muscle pair

A

one muscle contracts and the other relaxes

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2
Q

what is the structure of a skeletal muscle

A
  • made up of muscle fibres
  • cell surface membrane = sarcolemma
  • cytoplasm = sarcoplasm
  • endoplasmic reticulum = sarcoplasmic reticulum
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3
Q

what is the sarcolemma

A

cell membrane of a muscle fibre

folds to create deep tube like projections called t tubules

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4
Q

what does the sarcoplasm contain

A

mitochondria and myofibrils

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5
Q

what is the importance of lots of mitochondria in the sarcoplasm

A

carries out aerobic respiration to generate ATP for contraction

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6
Q

Importance of myofibrils in the sarcoplasm

A

made up of a bundle of actin and myosin filaments which slide past each other in contraction

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7
Q

Structure of myosin

A

thick filament
fibrous proteins with globular heads positioned away from the m line

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8
Q

structure of actin

A

thin filament made up of actin molecules
2 actin chains twist round to form one thin filament
tropomyosin is twisted around the two actin chains
troponin is also attached to the actin chain

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9
Q

microscopic structure of a skeletal muscle

A
  • sarcomere
  • m line
  • z line
  • H band
  • A band
  • I band
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10
Q

what is a sarcomere

A

section of myofibril between two z lines

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11
Q

what is a z line

A

attachment for actin filaments
end of a sarcomere

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12
Q

what is a m line

A

attachment for myosin filaments

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13
Q

what is an H band

A

section of muscle only containing myosin

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14
Q

what is an A band

A

section of muscle containing myosin and actin
where both filaments overlap

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15
Q

what is an I band

A

section of muscle only containing actin

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16
Q

breakdown of a muscle fibre

A

cell unit –> sarcoplasm –> myofibril –> sarcomere –> myosin and actin

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17
Q

what is tropomyosin

A

protein attached/twisted around two actin chains
prevents myosin heads binding to actin at rest

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18
Q

process of muscle contraction

A
  • Ca2+ diffuses out of the sarcoplasmic reticulum and into the myofibrils
  • Ca2+ binds to a protein attached to tropomyosin
  • this causes tropomyosin to change position on the actin and expose the myosin binding sites
  • myosin heads bind to actin and form a cross-bridge between the two filaments
  • Ca2+ stimulates ATP hydrolase
  • ATP is hydrolysed to ADP + Pi on the myosin head which causes the myosin head to bend
  • this pulls actin towards the centre of the sarcomere
  • ATP binds to myosin head which causes it to change shape and release from the actin and return to its original position
  • Myosin head is able to bind to new binding site
  • process repeats until muscle is fully contracted
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19
Q

what is a cross bridge formation

A

myosin head binds to actin binding site

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20
Q

how is a cross bridge formed

A

-Ca2+ binds to a protein which causes tropomyosin to change position and expose the myosin binding sites
- Myosin heads bind to actin filament forming a cross-bridge

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21
Q

What is the importance/role of ATP in the process of muscle contraction

A

ATP is required for the myosin head to detach from actin filament and return to original position

ATP is required for myosin heads to bend which allows actin to slide via hydrolysis

ATP required for the return of Ca2+ to the sarcoplasmic reticulum via active transport

22
Q

what is the role of phosphocreatine

A

molecule stored by muscles which can be used for rapid production of ATP when aerobic respiration is insufficient

23
Q

equation of the generation of ATP from phosphocreatine

A

ADP + phosphocreatine —> ATP + creatine

24
Q

characteristics of slow twitch muscles

A

lots of capillaries
lots of mitochondria
high concentration of myoglobin
slow contraction
fatigue less quickly
relies on aerobic respiration
red in colour

25
characteristics of fast twitch muscles
fewer capillaries fewer mitochondria less conc of myoglobin fast contraction fatigue quickly relies on anaerobic respiration pale in colour
26
example of a fast twitch muscle
eyelids
27
example of a slow twitch muscle
back
28
describe an inhibitory synapse
-prevent an action potential being generated - Cl- diffuse in K+ moves out hyperpolarisation occurs more Na+ is required to meet threshold and generate an action potential
29
what is visual acuity
resolution - ability to distinguish between two points
30
Why do cones have high visual acuity
- one cone cell is joined to a singular bipolar cell - sends separate impulses to the brain - brain is able to distinguish between the impulses
31
why do rods have low visual acuity
- multiple rods joined to a singular bipolar cell - sends general impulses to the brain - brain cannot distinguish between impulses
32
process of synaptic transmission across a cholinergic synapse
- action potential arrives at pre synaptic neurone and depolarises it - this causes Ca2+ voltage gated channels to open causing Ca2+ to move into the neurone via facilitated diffusion - causes vesicles containing Asch move and fuse with membrane - Asch diffuses across synapse and binds to receptors on membrane - Na+ channels open and Na+ moves in depolarising the neurone - if threshold is reached action potential is genarated - Asch is broken down or reabsorbed
33
describe the process of water reabsorption in the collecting duct
- water potential of the medulla is lower than the water potential of the filtrate in the collecting duct - collecting duct runs parrallel to ascending loop ( counter- current principle ) - water moves out of the collecting duct via osmosis
34
-nature of refractory period
period of time between impulses where the neurone is unable to be stimulated or generate another action potential as the K+ and Na+ channels are closed
35
importance of the refractory period
ensures the action potentials are discrete events means the impulse can only travel in one direction
36
stimulation of myogenic heartbeat
SAN depolarises and generates an action potential which causes the atria to contract impulses passes through non-conductive to the AVN which creates a delay in the impulse to allows the atria to finish contracting impulse is passed through the bundle to his to the purkyne fibres which causes the ventricles to contract from the bottom up
37
propagation along a non-myelinated neurone
- very slow depolarisation occurs along whole length of axon each section of axon is alternatively depolarised and repolarised
38
propagation along a myelinated neurone
- very fast allows saltatory conduction to occur impulse effectively jumps between the node of Ranvier's within the Schwann cells
39
generation of an action potential from the Paccinian corpuscle
-pressure stimuli causes the membrane to stretch and become distorted - this causes stretch mediated Na+ channels to open - Na+ diffuses into the Pacinian Corpuscle via facilitated diffusion and causes depolarisation which establishes a generator potential - if enough generator potentials are produced an action potential is generated
40
Structure of Pacinian Corpuscle
- layers of membrane separated by vicous gel containing Na+ ions - section of axon exposed to the PC contains stretch mediated Na+ channels
41
Process when glucose concentration is too low
- alpha cells in islets of langerhan in the pancreas detect low glucose concentration and releases glucagon - glucagon binds to specific receptors on liver and muscle cells - activates enzymes for gluconeogenesis and glycogenolysis - secreted until blood glucose levels return to normal
42
process of osmoregulation via ADH
- osmoreceptors in the hypothalamus detects low water potential in the blood and sends an impulse to the posterior pituitary gland which releases ADH - ADH binds to specific receptor proteins on the collecting duct - This stimulates vesicles containing aquaporfins to fuse with the membrane - This increases permeability of the duct so more water is absorbed via osmosis
43
process when glucose concentration is too high
- beta cells in the islets of langerhan in the pancreas detect an increase in glucose and release insulin - insulin binds to receptor proteins on liver and muscle cells and increases permeability of the cells to glucose by increasing rate of facilitated diffusion - also activates enzymes which stimulate glycogenesis
44
secondary messenger model
- glucagon or adrenaline binds to specific receptor proteins on the liver cell - this activates enzyme adenylate cyclase - this enzymes converts ATP to cyclic AMP - cyclic AMP activates protein kinase A - This stimulates a cascade of glycogenolysis reactions which increase levels of glucose in the blood
45
glycogenesis
conversion of glucose to glycogen activated by insulin decreases glucose concentration
46
glycogenolysis
hydrolysis of glycogen to glucose activated by glucagon increases glucose concentration
47
gluconeogenesis
conversion of amino acids and other organic substances to glucose activated by glucagon increases glucose concentration
48
what are the factors affecting speed of conduction
temperature, myelination and axon diameter
49
how does temperature affect speed of conduction
increasing temperature increases the kinetic energy available for facilitated diffusion of Na+ and K+ so rate of depolarisation increases
50
how does myelination affect speed of conduction
myeline sheath insulates the electrical impulse by allowing salatory condition to occur - impulse jumps between the nodes of ranvier
51
how does axon diameter affect speed of conduction
increased axon diameter means that axon membrane increased surface area - increases rate of diffusion of Na+ and K+ which increases the rate of depolarisation
52