muscle physiology Flashcards

(12 cards)

1
Q

What are the three types of contractile muscle cells in the human body?

A

Skeletal, cardiac, and smooth muscle.

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2
Q

What are the key features of skeletal muscle cells?

A

Multinucleated, striated, voluntary, attached to bones, involved in movement, posture, and metabolism.

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3
Q

What is excitation-contraction coupling in skeletal muscle?

A

Process by which an action potential triggers Ca²⁺ release from the SR, leading to muscle contraction via the sliding filament model.

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4
Q

Describe the sliding filament model of muscle contraction.

A

Myosin heads bind actin, pull filaments to shorten sarcomere; requires Ca²⁺ and ATP.

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5
Q

How do red and white skeletal muscle fibers differ?

A

Red fibers are slow, oxidative, and fatigue-resistant; white fibers are fast, glycolytic, and fatigue quickly.

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6
Q

What is the function of cardiac muscle?

A

Involuntary, striated muscle responsible for pumping blood through the heart.

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7
Q

What is the excitation-contraction coupling mechanism in cardiac muscle?

A

Depolarization leads to Ca²⁺ entry via L-type channels, triggering SR Ca²⁺ release (CICR), which activates contraction.

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8
Q

How does cardiac muscle differ from skeletal muscle?

A

Cardiac muscle has gap junctions, is involuntary, branched, and uses CICR instead of direct DHP-RyR coupling.

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9
Q

What is the function of smooth muscle?

A

Controls involuntary movements in internal organs like blood vessels, respiratory, GI, and urinary systems.

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10
Q

How does contraction in smooth muscle differ from skeletal muscle?

A

Smooth muscle uses calmodulin and MLCK instead of troponin; contraction is slower, longer-lasting, and energy-efficient.

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11
Q

What is unique about smooth muscle excitation-contraction coupling?

A

It can involve second messengers (e.g., IP₃, cAMP, NO) and is initiated by hormones or neurotransmitters as well as voltage changes.

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12
Q

How do the three muscle types compare in contraction mechanism?

A

All use actin, myosin, ATP, and Ca²⁺; differ in Ca²⁺ source, regulatory proteins, and coupling mechanisms.

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