SKELETAL PT 2 Flashcards

1
Q

describe how muscle fiber type shifts

A

with loading (exercise training), IIX goes down and with unloading (like a space flight or spinal cord injury), IIX amount goes up

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2
Q

why do IIX fibers increase with inactivity

A

because I and IIA use a lot of oxygen, so it’s a lot of work to keep them up

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3
Q

describe aerobic training and muscle fiber type

A

less IIA, more I

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4
Q

describe motor units

A

vary in size; consists of a motor neuron and all muscle fibers they supply

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5
Q

how are muscle fibers dispersed through a muscle

A

muscle fibers from a motor unit spread throughout the whole muscle, so stimulation of a single motor unit causes only weak contraction of muscle

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6
Q

what principle so motor units follow

A

all or none principle

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7
Q

what are the three types of muscle fibers

A

type I (slow), type IIA (fast fatigue-resistant), type IIX (fast fatiguable)

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8
Q

describe type IIX motor fibers

A

fast fatiguable, large motor units with high innervation ratio, fast twitch

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9
Q

describe IIA motor fibers

A

large motor units, more sustained but less dramatic twitch; more fatigue resistant but still fatiguable

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10
Q

describe type I fibers

A

small motor neurons, low innervation ratio, slow twitch and fatigue resistant

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11
Q

what is excitation-contraction coupling

A

process of pairing electrical events (motor neuron AP) to mechanical events (muscle contraction); aka events that occur between excitation and coupling

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12
Q

where does EC coupling occur

A

synapse of junction of motor neuron axon terminal with muscle fiber motor end plate (very excitable region of muscle fiber plasma membrane)

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13
Q

what neurotransmitter is released at neuromuscular junction

A

acetylcholine

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14
Q

describe the first step of EC coupling process

A

have signal that sent do somatic motor neuron,
which is a depolaorizing event

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15
Q

describe the second step in EC process

A

at neuromuscular junction, we release Ach, which binds
to receptors on skeletal muscle membrane, which allows for depolairzation
of skeletal muscle membrane

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16
Q

describe the third step in EC process

A

opening of Na channels, which causes influx of Na which causes depolirzation

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17
Q

describe the fourth step in the EC process

A

depolariization goes down t-tubules; along t-tubules on either side is a bunched up
part of the sarcoplasmic reticulum

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18
Q

describe the 5th step in the EC coupling process

A

ca binds to tropnin, which tells tropomyosin to move from actin

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19
Q

describe the sixth step of EC process

A

myosin can bind to actin and allow for contraction

20
Q

whats the cross bridge

A

binding site of ATP on each molecule

21
Q

what is cross bridge formation triggered by

A

Ca2+ cycle

22
Q

whats the first step in cross bridge formation

A

active site on actin is exposed as Ca binds to troponin

23
Q

whats the second step in cross bridge formation

A

myosin head forms a cross-bridge with actin

24
Q

whats the third step of cross bridge formation

A

during power stroke, myosin head bends and ADP and phosphate are released

25
whats the fourth step in cross bridge formation
a new molecule of ATP attaches to the myosin head, causing the cross-bridge to detach
26
whats the fifth step in crossbirdge formation
ATP hydrolyzes to ADP and phosphate, which returns myosin to cocked position
27
describe the skeletal muscle length-tension relationship
describes the amount of tension that is produced by a muscle as a feature of it's length
28
what are skeletal muscle satellite cells
skeletal muscle stem cells, that are multipotent and give rise to more satellite cells, differtnited skeletal muscle cells, myonuclei
29
how much nuclear material belongs to true myonuclei
85 - 95% (i.e. located inside plasma membrane)
30
how much of nuclear material are satellite cells
5 - 15%; located between basement membrane and plasma membrane
31
how many nuclei per fiber length do satellite cells have
approx. 200 - 300 nuclei per mm of fiber length (contrast to many other cells in our body which are usually single nucleus)
32
why are satellite cells/myonuclei important
growth + development of muscle adaptive capacity of skeletal muscle recovery from injury or neuromuscular disease
33
where is nuclear material located
between myofiber basement and plasma membrane
34
describe satellite cell role in myofiber hypertrophy
not completely known; but as fiber grows, there is need for new myonuclei to maintain myonuclear domains
35
whats the myonuclear domain theory
every nuclei within the muscle fiber is responsible for a specific amount of volume within the cell, so we can only make muscle grow if we get more nuceli involved so satellite cells donate
36
describe the first step in myonuclear donoation
untrained muscle fiber
37
describe the second step in myofiber donation
training muscle fiber increases in size; each myonuclei is near its domain ceiling
38
describe the third step in myonuclei donation
satellite cells fuse to the muscle fiber, donating nuclei
39
describe the fourth step of myofiber / myonuclear donation
muscle fiber now has more nuclei; therefore, it's growth capacity has increased
40
different between the two possible response to fiber stress
hypertrophy (fibers grow in size - humans); hyperplasia (fibers grow in number)
41
describe regenerating normall musclle fiber
myonuclei + satellite cell
42
describe regenerating damaged muscle fiber
activated + proliferating satellite cells
43
describe regenerating repairing muscle fibers
muscle precursors cells derive from satellite cells have fused
44
describe generating regenerated muscle fibers
with new satellite cell and centrally-placed, newly-generated myonuclei
45
describe the calcium/tropnonin/tropomyosin relationship
Ca connects to troponon, which tells tropomyosin to get off binding sites so myosin can attach
46
where is calcium stored and what happens when that thing is depolarized
Ca stores in sarcoplasmic reticulum; when depolaorized, Ca ion channels open up and let Ca into sarcoplasm which lets everything happen
47
what are the three parts of the power stroke
- adp and P on myosin = myosin can grab actin - adp and P leave myosin, nothing on myosin and can pull in - atp on myosin, myosin releases actin