2 - Green - Muscle Physiology II Flashcards

1
Q

Active Tension

A

Force generation by formation of actin-myosin crossbridges

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2
Q

Cachexia

A

Dramatic muscle atrophy seen in patients with chronic illness

“wasting syndrome”

AIDS, cancer, diabetes, MS

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3
Q

Isometric Contraction

A

length constant, tension changes

Object too heavy to pickup

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4
Q

Isotonic Contraction

A

Tension constant, length changes

Bicep curls for the girls

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5
Q

Motor Unit

A

Single Motor neuron and all muscle fibers it innervates

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6
Q

Myopathy

A

Disease of skeletal muscle not caused by nerve disorders

Congenital, genetic abnormalities in Mt, glucose/glycogen metabolism defects

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7
Q

Myositis

A

Inflammation of skeletal muscles

Muscles closest to trunk

Causes: Injury, infection, autoimmune disease

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8
Q

Rhabdomyolysis

A

Rapid destruction of muscle cells

Muscle proteins in urine–very dark urine

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9
Q

Sarcopenia

A

Age-related reduction in skeletal muscle mass and strength

normal , not disease related

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10
Q

Total Tension

A

Force generated by cross bridge formation and stretching muscle tension

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11
Q

Concentric

v

Eccentric

A

Concentric - muscle decreasing in length against opposing load–lifting weight up

Eccentric - muscle increasing in length as it resists load–pushing weight down

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12
Q

Optimal Length (Lo)

A

Length of muscle where maimum force is generated

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13
Q

What occurs if muscle is stretch too far?

Too close?

A

Little actin/myosin overlap, few corssbridges–low tension

Too much overlap, crowded, cross bridges weakened–low tension

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14
Q

What is the majority of tension in the normal working range of muscle?

A

Majority from active tension–actin/myosin crossbridges

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15
Q

Passive Tension

A

Inherent property of muscle fiber, generated by stretching muscle to different lengths

not caused by actin-myosin crossbridges

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16
Q

What is the mechanical advantage gained by muscular attachment points?

A

Fulcrum advantage, joint moves small compared to distal end of moment arm

17
Q

Force-Velocity Relationship of Muscle

A

More load, slower velocity.

Vmax when load = 0

18
Q

Load Velocity is Directly Proportional to what?

A

Number of crossbridges formed

19
Q

Type I Fibers:

AKA

Mitochondria?

Source of Energy?

Color?

Fatigue?

Motor Neuron Size?

Uses?

A

Slow-Twitch

Slow myosin ATPase

High Mitochondria

Cellular Respiration (Aerobic)

Red (high myoglobin)

Resistant to fatigue

Small, slow conductiong motor neurons

Running marathons

20
Q

Type IIa Fibers:

AKA

Mitochondria?

Source of Energy?

Color?

Fatigue?

Motor Neuron Size?

Uses?

A

Fast Twitch

Fast myosin ATPase

High mitochondria

Cellular respiration, low glycolysis

Red-Pink (high myoglobin)

Semi fatigue resistant

Intermediate, fast-conducting motor neurons

Sprinting, walking

21
Q

Type IIb Fibers:

AKA

Mitochondria?

Source of Energy?

Color?

Fatigue?

Motor Neuron Size?

Uses?

A

Fast Twitch

Fast myosin ATPase

Low Mitochondria

Rich in Glycogen

Glycolysis

White (low myoglobin)

Fatigue Easily

Large, fast-conducting motor neurons

Hitting a baseball

22
Q

Innervation Ratio

A

Number of fibers innervated by motor unit

23
Q

Type I Motor Units

A

Few fibers innervated – small ratio

Slow conducting

Fine, graded movements

24
Q

Type II Motor Units

A

Large diameter, large ratio

Faster-conducting

Coarse movements

25
Q

What two ways can tension be increased in muscle?

A

Recruitment - increasing motor units contracting

Summation - Increasing frequency of individuals motor unit firing

26
Q

In what order are muscle fibers recruited?

A

Type I (slow) first

Type II (fast) second

27
Q

What are some proposed causes for muscular fatigue

A

Glycogen / creatine phosphate depleted

ATP levels do NOT decrease substantially

decreased motor neuron firing

decreased O2

impaired Ca2+ release

28
Q

Muscle Cells in Aging

Motor Units in Aging

A

Atrophy

Fewer satellite cells

reduced mitocondria

Reduced number

Increase in number of fibers/motor unit (motor neuron loss)

29
Q

Muscular Dystrophy

A

Progressive skeletal muscle weakness, defect in muscle proteins, death of muscle cells and tissues

Duchenne / Becker

Mutation in dystrophin gene

Instability of sarcolemma–damage during contractions

30
Q

Malignant Hyperthermia

A

Defect in RYR1 Channel

Open easily, close slowly

Anesthetics, muscle relaxers

Uncontrolled Ca2+ release

Rigidity / Heat production