Muscle Contraction Flashcards

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

A

little/no

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
A

neuropathies

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

A

myopathies

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

A

hypocalcemia

25
Q

________ is a presynaptic disorder marked by weakness due to continuous depolarization and spontaneous EMG activity (increased synaptic vesicle release)

A

hypercalcemia

26
Q

______ causes a presynaptic disorder described as ‘functional denervation’. Presynaptic binding inhibits acetylcholine release.

A

botulinum toxin

27
Q

3 post-synaptic neuromuscular disorders

A
  • muscular dystrophy
  • myasthenia gravis
  • Conotoxin
28
Q

_________: post-synaptic disorder caused by the lack of the structural protein dystrophin

A

muscular dystrophy

29
Q

What condition is described by the following symptoms?

  • leaky muscle cells, high creatine kinase levels
  • progressive weakness
  • EMG shows repetitive high frequency discharges
A

muscular dystrophy

30
Q

_________: post-synaptic disorder in which acetylcholine receptors are destroyed (or genetically reduced in numbers)

A

Myasthenia gravis

31
Q

What is the treatment for Myasthenia Gravis?

A

acetylcholinesterase inhibitors

32
Q

In which condition is acetylcholine destroyed before it can become receptor bound?

A

Myasthenia Gravis