Muscle Contraction Flashcards

(32 cards)

1
Q

sarcomeres change ______ during muscle depolarization

A

length

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2
Q

The _____ segment of myosin has ATP and actin binding sites

A

S-1

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3
Q

the heavy myosin chains form the ____ region and the light myosin chains form the ______ region of the molecule

A
  • tail

- globular head

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4
Q

myosin filaments form structures with 2 polypeptides in a ______ arrangement

A

alpha-helix (the tail region)

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5
Q

myosin heads project off of the thick filament every ____ degrees

A

60

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6
Q

_______: a 40 nm long fibrous protein that spans 7 G-actin myosin binding sites (inhibitory protein)

A

tropomyosin

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7
Q

during muscle relaxation, ______ is elevated out of the actin helical groove

A

tropomyosin

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8
Q

Ca++ binds to ______, which regulates the movement of tropomyosin

A

troponin

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9
Q

The Length-Tension Relationship states that force is proportional to __________

A

crossbridge overlap

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10
Q

___________: a single motor neuron and all of the muscle fibers it innervates

A

motor unit

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11
Q

a single motoneuron will innervate _________ to __________ muscle fibers

A

hundreds to thousands

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12
Q

the fibers of a single motor neuron are all __________ similar

A

biochemically

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13
Q

the ___________ describes the relationship between the number of muscle fibers innervated by a motoneuron and the degree of control exerted

A

innervation ratio

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14
Q

fine motor control occurs with a ____ fiber:neuron ratio and coarse motor control occurs with a _____ fiber:neuron ratio

A
  • low

- high

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15
Q

skeletal muscle has a ________ type acetylcholine receptor

A

nicotinic

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16
Q

___________ or __________ can also activate muscle, but are inactivated more slowly than acetylcholine

A
  • nicotine

- carbamylcholine

17
Q

Muscle Action Potential (MAP) triggers conformational changes in the ______________ proteins

A

DHP/Ryanodine receptor-like proteins

18
Q

normal muscle at rest should have ________ EMG activity

19
Q

_________ is associated with the slowing of nerve conduction velocity

A

demyelination

20
Q

__________ are disease states of the following cell types:

  • cell bodies
  • axons
  • Schwann cells
  • mixed
21
Q

________ are disease states associated with the following structures:

  • presynaptic - axon terminals
  • synaptic cleft
  • postsynaptic - sarcolemma
A

junctionopathies

22
Q

_________ are disease states associated with the myofibers

23
Q

3 presynaptic muscle disorders

A
  • hypocalcemia
  • hypercalcemia
  • botulinum toxin
24
Q

______ is a presynaptic disorder marked by weakness, tetany, spontaneous EMG activity, and reduced acetylcholine release

25
________ is a presynaptic disorder marked by weakness due to continuous depolarization and spontaneous EMG activity (increased synaptic vesicle release)
hypercalcemia
26
______ causes a presynaptic disorder described as 'functional denervation'. Presynaptic binding inhibits acetylcholine release.
botulinum toxin
27
3 post-synaptic neuromuscular disorders
- muscular dystrophy - myasthenia gravis - Conotoxin
28
_________: post-synaptic disorder caused by the lack of the structural protein dystrophin
muscular dystrophy
29
What condition is described by the following symptoms? - leaky muscle cells, high creatine kinase levels - progressive weakness - EMG shows repetitive high frequency discharges
muscular dystrophy
30
_________: post-synaptic disorder in which acetylcholine receptors are destroyed (or genetically reduced in numbers)
Myasthenia gravis
31
What is the treatment for Myasthenia Gravis?
acetylcholinesterase inhibitors
32
In which condition is acetylcholine destroyed before it can become receptor bound?
Myasthenia Gravis