Skeletal Muscle Flashcards

1
Q

3 Troponin Subunits and Functions

A

Tn-T - binds to tropomyosin
Tn-C - binds Ca++
Tn-I - binds actin, inhibiting contraction

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2
Q

Crossbridge Cycle

A

Muscle is energized w/ ADP and Pi, still retains energy from ATP
W/ Ca, binds to actin and releases ADP/Pi for power stroke/rotation, moving it like 10nm
ATP displaces actin, and ATPase activity of myosin head brings back to start

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3
Q

Triad Components

A

2 SR Lateral Cisternae and a T-tubule

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4
Q

SERCA

A

SR Calcium ATPase, that uses ATP to transport 2 Ca from sarcoplasm into SR lumen to clear all Ca after contraction. In high concentrations on lontidudinal cisternal membrane

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5
Q

Calsequestrin

A

Sequesters calcium in SR

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6
Q

2 Prots involved w/ Ca Release from SR

A

Dihydropyridine R (DHPR) is like a Vg Ca channel but doesn’t have a pore. Sits on T-tubule membrane and moves w/ depol, unplugging Ca release channel on SR membrane, allowing Ca to leave into sarcoplasm

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7
Q

4 Sources of ATP in Muscle Cell (shortest to longest duration of supply)

A

Free ATP
Creatine Phosphate
Glucose/Glycolysis
Pyruvate/Krebs and OXPHOS

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8
Q

5 Differences b/w Slow and Fast (Red and White) Muscle Fibers

A
Small vs. Large Fibers
High vs. Low Myoglobin Conc
Many vs. Few mt
High vs. Low Fatigue Resistance
Moderate vs. Very High Glycogen Stores
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9
Q

2 Mechs to Generate More Force

A
  1. Increase stimulation frequency

2. Increase recruitment of more muscle fibers

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10
Q

Tetanic Frequency

A

Max stimulation frequency after which no further increases of force sustained

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11
Q

Isotonic vs. Isometric Contractions

A

Muscle undergoes shortening while tension remains constant vs. experiencing max tension with no change in length

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12
Q

Duchenne Muscular Dystrophy

A

Problem w/ dystrophin, one of complex of prots that links IC cytoskeleton to EC matrix so you get progressive tearing of muscles

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13
Q

Nebulin

A

Finite rod-shaped protein acts as molecular ruler in striated muscle to determine actin filament length or else the globules assemble infinitely. Mutations can cause late-onset dystrophy

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14
Q

Titin

A

Largest prot in genome, acts as scaffold from Z line to center for thick/thin filaments

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15
Q

alpha-actinin

A

in all 3 types to anchor thin filaments (either with dense bodies or Z lines)

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