muscle physiology Flashcards

1
Q

how are muscles attached to the skeleton?

A

via tendons

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2
Q

describe the structure of a myofilament

A

protein complexes formed from large numbers of myosin II molecules. the myosin heads contain regulatory light chain and an alkali light chain. there is a hinge region and an a-helical tail region of heavy chains

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3
Q

what are the thin filaments (skeletal) formed from?

A

actin in complex with troponin and tropomyosin

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4
Q

what is the calcium sensor in skeletal muscle?

A

troponin

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5
Q

outline the cross bridge cycle

A

1- ATP binds to myosin head
2- ATP is hydrolysed, myosin head returns to resting position
3-cross bridge forms at a new position on actin
4-P is released and a conformational change results in the power stroke

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6
Q

how does the crossbridge cycle in skeletal muscle differ from the crossbridge cycle in smooth muscle?

A

in skeletal muscle, the myosin head has constant ATPase activity, meaning the crossbridge cycle will occur constantly as long as Ca2+ and ATP are elevated. in smooth muscle, ATPase activity requires a phosphorylation event, meaning that crossbridge cycle is prolonged without constant ATP use

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7
Q

explain how [Ca2+] regulates contraction in skeletal muscle when Ca2+ is low

A

when [Ca2+] is low, tropomyosin sterically hinders the crossbridge cycle by obscuring the myosin binding site

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8
Q

explain how [Ca2+] regulates contraction in skeletal muscle when Ca2+ is high

A

the tropomyosin-troponin complex undergoes a conformational change, exposing the myosin binding site

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9
Q

what is a ‘triad’?

A

found in skeletal muscle; 2 sarcoplasmic reticulum with a T-tubule sandwiched between

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10
Q

how is calcium release in the cytoplasm controlled in skeletal muscles?

A

dihydropyridine receptors are voltage-gated receptors found on the T-tubule, when depolarised, they cause ryanodine receptors on the sarcoplasmic reticulum to open, triggers release of Ca2+ into cytoplasm

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11
Q

outline excitation-contraction coupling in skeletal muscle

A

1) end plate potential triggers AP in muscle fibre
2) AP propagates along sarcolemma down the T-tubules
3) depolarisation of T-tubules is sensed by dihydropyridine receptors, which are mechanically coupled to RYR
4) RYR opens, and Ca2+ released into cytoplasm
5) influx of Ca2+ initiates the cross-bridge cycle
6) Ca2+ pumped back into the SR by SERCA

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12
Q

which factors determine the force of contraction?

A
  • frequency of action potentials
  • number of motor units activated
  • active length of the muscle
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13
Q

why does a full tetanus occur when frequency of APs is high?

A

the effect of the APs on force exerted is summative

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14
Q

what is meant by ‘passive force’?

A

when you stretch a muscle without electrically stimulating it, and the force increases with length

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15
Q

what is meant by ‘total force’?

A

the force production when a muscle is stretched and electrically stimulated at the same time

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16
Q

how is active force of a muscle worked out?

A

total force - passive force

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17
Q

compare cardiac muscle with skeletal muscle

A

cardiac muscle: smaller cells, electrically and mechanically coupled using gap junctions and desmosomes
skeletal muscle: individual cells are smaller, and mechanically coupled

18
Q

explain how the heart is myogenic

A

the threshold in the SA node is reached spontaneously, no external depolarisation is required

19
Q

outline the conduction system of the heart

A

1) the SA node is the primary pacemaker region
2) action potentials spread across the atria
3) atrioventricular node is the secondary pacemaker region
4) conduction propagates through AVN along ventricular conduction system consisting of purkinje fibres

20
Q

what is the role of cardiac refractory periods?

A
  • allows ventricles to fill with blood

- protects heart from premature depolarisation

21
Q

on what are dihydropyridine receptors and ryanodine receptors in the cardiac muscle dependent on?

22
Q

how should Frank Starling’s law of the heart be interpreted?

A

the amount of blood returning to the heart determines how much the muscle is stretched, and thus how much force is generated

23
Q

why is it important that there is a strong passive component of tension in cardiac muscle?

A

as stretching increases, force production decreases due to less crossbridge cycling. the passive component of tension prevents overextension of the muscle

24
Q

how is positive inotropy induced?

A

adrenaline and noradrenaline interact with ventricular B1-adrenoceptors

25
what is the calcium sensor in smooth muscle?
calmodulin
26
give the roles/responsibilities of smooth muscle
- regulation of blood pressure - peristalsis in the digestive system - ciliary muscles in the eye - piloerection
27
how does the structure of smooth muscle differ from striated muscle? what is the implication of this difference?
there are no Z-lines in smooth muscle, Z-lines are responsible for preventing overextension. smooth muscle is able to extend much further than striated muscle
28
give 3 mechanisms for the regulation of smooth muscle contraction
1- synaptic inputs from the ANS 2- circulating hormones/metabolites 3-intrinsic activity of pacemaker cells
29
what is meant by 'multi-unit' regulation of contraction? what function is this used for?
electrical isolation of individual muscle cells. used for fine motor control
30
what is meant by 'unitary' regulation of contraction?
cells are electrically coupled by gap junctions for coordinated contraction
31
how does intracellular and extracellular sources of calcium differ in smooth muscle?
- the SR is smaller and less organised | - no T-tubules, invaginations called caveoli instead
32
explain a pathway which allows smooth muscle to contract independent of a change in membrane potential
IP3 binds to IP3 receptor and triggers release of Ca2+. dependent on the activation of Gaq-coupled GPCRs
33
what are the sarcolemmal pathways for calcium influx?
- voltage gated calcium channels - ligand gated calcium channels - store operated calcium channels
34
how is the regulatory light chain on the myosin head of the myofilament responsible for regulation of contraction in smooth muscle?
the RLC must be phosphorylated to permit ATPase activity of myosin myosin light chain kinase is activated when Ca2+ binds calmodulin
35
what is meant by 'latch state'? explain how it occurs
smooth muscle can maintain prolonged contraction without using much ATP - as ATP is hydrolysed, Ca2+ falls, and MLCK activity decreases - this means ATPase activity is slowed alongside crossbridge cycling - myosin head remains bound to actin, force prolonged
36
stimulation of which receptors causes contraction of smooth muscle?
- a1-adrenoceptors - M1-muscarinic receptors - H1-Histamine receptors
37
stimulation of which receptors causes relaxation of smooth muscle?
- B-adrenoceptors - D1-dopamine agonists - H2-histamine receptors
38
what is the common feature of the G-as coupled receptors which cause relaxation of smooth muscle?
they all result in increased adenylyl cyclase activity, causing amount of cAMP to rise -> PKA stimulation -> reduced MLCK activity
39
what is exploited pharmacologically to stimulate contraction of smooth muscle?
- intracellular [Ca2+] increase | - increasing sensitivity of myofilaments to calcium
40
what is exploited pharmacologically to stimulate relaxation of smooth muscle?
- reducing intracellular calcium | - inhibiting contraction of myofilaments