Muscle Physiology Flashcards

1
Q

Describe skeletal muscle.

A
  • Cylindrical
  • Under voluntary control
  • Multinucleated
  • Striated
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2
Q

Describe smooth muscle.

A
  • Under involuntary control
  • Mononucleated
  • Non-striated
  • Found in hollow organs
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3
Q

Describe cardiac muscle

A
  • Under involuntary control
  • Mono/binucleated
  • Striated
  • Branched
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4
Q

How are skeletal muscle fibres arranged?

A
  • Muscle composed of groups of muscle fibres
  • Fibres bundled into fascicles
  • Within muscle fibres are myofibrils
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5
Q

Describe muscle fibre cell structure. PART 1

A
  • Cells wrapped in sarcolemma
  • Invaginations in sarcolemma - T-Tubules descend into cells and wrap around myofibrils
  • Tubules increase SA for ion transfer between ECF and ICF
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6
Q

Describe muscle fibre cell structure. PART 2

A
  • SR wrapped around myofibrils - store of calcium ions
  • Terminal cisternae at ends of SR
  • Point where cisternae meets T-tubules is the triad
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7
Q

Describe myofibril structure.

A
  • Striated due to intraccellular cytoskeletal proteins
  • Made up of myosin and actin chains
  • Functional units are sarcomeres
  • Tropomyosin wrapped around actin chains with troponin on its surface
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8
Q

What is the relationship between muscle fibres and motor neurons?

A
  • Muscle fibre innervated by single motor neuron
  • Motor neurons. innervate multiple fibres
  • In areas that require fine control, motor neuron will only innervate few muscle fibres.
  • OPPOSITE FOR AREAS THAT DON’T NEED FINE CONTROL
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9
Q

Outline what occurs at the neuromuscular junction. PART 1

A
  • Pre-synaptic terminals release ACh which bind to post-synaptic nAChRs
  • Ion channels activate causing sodium influx and cause action potential
  • Wave of depolarisation induced which reaches T-junction.
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10
Q

Outline what occurs at the neuromuscular junction. PART 2

A
  • Wave of depolarisation reaches T-tubules
  • Activates VGCCs allowing influx of extracellular calcium into cell
  • Channels connected to RyRs on wall of SR
  • When RyRs activated, conformational change in RyRs
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11
Q

Outline what occurs at the neuromuscular junction. PART 3

A
  • RyR activated and calcium flows into cell
  • Rise in intracellular calcium and myofibrils contract
  • Removal of calcium through SERCA2 (back into SR) and sodium-calcium exchanger (out of cell in exchange for sodium)
  • Myofibrils relax
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12
Q

What happens in the cross bridge cycle? PART 1

A
  • When relaxed, actin chains bound by troponin and tropomyosin. Prevent myosin binding
  • Myosin bound by ADP, are ‘cocked’
  • Calcium binds to troponin C following rise in intracellular calcium
  • Myosin binding sites are exposed as troponin released
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13
Q

What happens in the cross bridge cycle? PART 2

A
  • Myosin binds
  • Conformational change causing movement of myosin head
  • Causes movement of Z bands closer together
  • ADP released from myosin and ATP binds causing release of myosin head from actin.
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14
Q

What happens in the cross bridge cycle? PART 3

A
  • Reduction in intracellular calcium. Troponin reinstated and binding sites blocked
  • ATP hydrolysed back to ATP
  • Myosin head moved back into cocked position
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15
Q

Why does rigor mortis occur?

A
  • Rise in intracellular calcium
  • Actin binding sites exposed
  • Myosin binds
  • No ATP available to remove myosin heads from actin binding sites
  • Continuous contraction
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16
Q

Describe Type 1 fibres

A
  • ‘Slow twitch’ - used when long-term sustained contractions requireed
  • ATP synthesised by oxidative metabolism
  • Require high oxygen supply so large amounts of myoglobin to facilitate this
17
Q

Describe Type IIa fibres.

A
  • Utilise oxidative and anaerobic metabolism
  • Anaerobic metabolism - fast but inefficient so contraction is rapid
  • Oxidative metabolism allows fibres to be slightly fatigue resistant
18
Q

Describe Type IIb fibres.

A
  • Fast twitch - reliant on anaerobic metabolism
  • Don’t have large amounts of myoglobin/mitochondria
  • Easily fatigable
19
Q

Describe cardiac muscle

A
  • Muscle cells joined by gap junctions
  • Allows for spread of depolarisation to neighbouring cells (initiated from SAN)
20
Q

Describe electrical-contraction coupling in cardiac muscle.

A
  • Calcium entry into cell from extracellular spaces at T-tubules
  • Activates RyRs - causing calcium release from SR
  • Calcium interacts with myosin and actin to cause contraction
  • Removal by SERCA and NCX exchanger
21
Q

Describe multiunit smooth muscle cells.

A
  • Exist as separate entities stimulated by their own motor nerves
  • Behave independently
  • Have swellings called varicosities which are pre-synaptic terminals
22
Q

Describe unitary smooth muscle cells.

A
  • Most common type
  • SMCs joined by gap junctions - allowing for passage of depolarising ions from cell to cell
  • Only a few muscle cells need to be innervated by autonomic neurons
  • Portion of muscle that contracts are functional units
23
Q

Describe autonomic-mediated smooth muscle contraction

A
  • Activation of Gq linked GPCRs
  • Increase intracellular IP3
  • Binds to IP3 receptors on SR causing calcium release into cytosol
23
Q

What is another autonomic mediated method of muscle contraction?

A
  • Opening of calcium ion channels
  • Activates ryanodine receptors in SR - calcium released into cytosol
  • Calcium channels close once threshold met
  • Activity of neighbouring cells influenced by gap junctions
24
Q

What is the difference between skeletal/cardiac and smooth muscle contraction?

A
  • Smooth muscle contraction - dependent on calcium influx (not sodium)
  • Smooth muscle contraction slower - calcium channels open slower than sodium channels