muscle physiology flashcards

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24 Terms

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epimysium

a fibrous connective tissue sheath that surrounds the entire muscle

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fascicle

a bundle of skeletal muscles

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endomysium

a connective tissue sheath surrounding each muscle fiber that contains capillaries and nerves

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perimysium

a connective tissue sheath surrounding several muscle fibers

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motor unit

comprised of a single motor neuron and all of the muscle fibers it innervates

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neuromuscular junction (NMJ)

specialized synapse between the somatic (α) motor neuron’s nerve terminal and the motor end plate of the skeletal muscle cell

<p>specialized synapse between the somatic (α) motor neuron’s nerve terminal and the motor end plate of the skeletal muscle cell</p>
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excitation/contraction (E/C) coupling

transformation of this electrical signal (in the muscle cell) into contraction of sarcomeres

muscle action potentials sensed in t-tubules trigger Ca2+ release from the SR and cause muscle contraction

process:

  1. action potential travels along sarcolemma of muscle fiber

  2. action potential reaches t-tubules, allowing the action potential to rapidly penetrate into the interior of the muscle fiber

  3. voltage-gated calcium channels in the SR membrane open in response to action potential, causing a rapid influx of calcium ions from the SR into the cytoplasm of the muscle fiber

  4. the released calcium ions bind to troponin, a protein located on the actin filaments within the muscle fiber

  5. troponin binding causes a conformation change in the troponin-tropomyosin complex, exposing active sites on the actin filaments

  6. myosin heads bind to the exposed active sites on the actin filaments, forming cross-bridges

  7. the myosin heads undergo a power stroke, causing thin filaments to slide over the thick filaments, shortening the sarcomere and resulting in muscle contraction

<p>transformation of this electrical signal (in the muscle cell) into contraction of sarcomeres</p><p>muscle action potentials sensed in t-tubules trigger Ca2+ release from the SR and cause muscle contraction</p><p>process:</p><ol><li><p>action potential travels along sarcolemma of muscle fiber</p></li><li><p>action potential reaches t-tubules, allowing the action potential to rapidly penetrate into the interior of the muscle fiber</p></li><li><p>voltage-gated calcium channels in the SR membrane open in response to action potential, causing a rapid influx of calcium ions from the SR into the cytoplasm of the muscle fiber</p></li><li><p>the released calcium ions bind to troponin, a protein located on the actin filaments within the muscle fiber</p></li><li><p>troponin binding causes a conformation change in the troponin-tropomyosin complex, exposing active sites on the actin filaments</p></li><li><p>myosin heads bind to the exposed active sites on the actin filaments, forming cross-bridges</p></li><li><p>the myosin heads undergo a power stroke, causing thin filaments to slide over the thick filaments, shortening the sarcomere and resulting in muscle contraction</p></li></ol>
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troponin

protein located on the actin filaments within the muscle fiber

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t-tubule

invaginations of the sarcolemma that extend deep into muscle fiber and allows rapid transmission of action potentials from the surface of the muscle fiber to the interior

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sarcoplasm

cytoplasm of the muscle cell

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sarcolemma

plasma membrane of the muscle cell

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actin

protein that produces thin contractile filaments within muscle cells

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myosin

protein that produces dense contractile filaments within muscle cells

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steps from motor neuron action potentials to skeletal muscle contractions

  1. acetylcholine binds to skeletal muscle fibers (nicotinic receptors)

  2. action potentials moves into t-tubules

  3. Ca2+ release by sarcoplasmic reticulum (trigger for contraction)

  4. Ca2+ binds to troponin; active cross-bridge cycling

  5. skeletal muscle contraction

  6. acetylcholinesterase in cleft of NMJ degrades acetylcholine

  7. Ca2+ pumped into extracellular fluid and SR

  8. tropomyosin blocks cross-bridge formation

  9. skeletal muscle contraction is prevented

<ol><li><p>acetylcholine binds to skeletal muscle fibers (nicotinic receptors)</p></li><li><p>action potentials moves into t-tubules</p></li><li><p>Ca2+ release by sarcoplasmic reticulum (trigger for contraction)</p></li><li><p>Ca2+ binds to troponin; active cross-bridge cycling</p></li><li><p>skeletal muscle contraction</p></li><li><p>acetylcholinesterase in cleft of NMJ degrades acetylcholine</p></li><li><p>Ca2+ pumped into extracellular fluid and SR</p></li><li><p>tropomyosin blocks cross-bridge formation</p></li><li><p>skeletal muscle contraction is prevented</p></li></ol>
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sarcomere

the repeating structural unit of myofibrils in striated muscle; area between consecutive z-lines, consisting of a dark band in the middle and a light band on either side; smallest contracile unit of a muscle cell

  • thin filaments: actin

  • thick filaments: myosin

sarcomeres shorten during muscle contraction due to thick and thin filaments sliding past one another

<p>the repeating structural unit of myofibrils in striated muscle; area between consecutive z-lines, consisting of a dark band in the middle and a light band on either side; smallest contracile unit of a muscle cell</p><ul><li><p>thin filaments: actin</p></li><li><p>thick filaments: myosin</p></li></ul><p><strong>sarcomeres shorten during muscle contraction due to thick and thin filaments sliding past one another</strong></p>
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parts of a sarcomere

  • z-discs (z-lines): borders between neighboring sarcomeres; appears as a dark line in the middle of the I-band

  • a-band: length of thick filament; dark area of striation and identifies location of myosin filaments

  • m-line: center of sarcomere

  • i-band: region of thin filaments without any overlapping thick filaments; only consists of actin

  • h-zone: region of thick filaments without any overlapping thin filaments, only consists of myosin

<ul><li><p>z-discs (z-lines): borders between neighboring sarcomeres; appears as a dark line in the middle of the I-band</p></li><li><p>a-band: length of thick filament; dark area of striation and identifies location of myosin filaments</p></li><li><p>m-line: center of sarcomere</p></li><li><p>i-band: region of thin filaments without any overlapping thick filaments; only consists of actin</p></li><li><p>h-zone: region of thick filaments without any overlapping thin filaments, only consists of myosin</p></li></ul>
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muscle contraction (filaments)

  • shortening of sarcomeres via sliding of thin filaments (actin) towards m-lines

    • thick and thin filament lengths are constant but overlap incrases

    • a-bands maintain their length

    • i-bands and h-zones narrow

→shortening of myofibrils → shortening of muscle cell → muscle contraction

<ul><li><p>shortening of sarcomeres via sliding of thin filaments (actin) towards m-lines</p><ul><li><p>thick and thin filament lengths are constant but overlap incrases</p></li><li><p>a-bands maintain their length</p></li><li><p>i-bands and h-zones narrow</p></li></ul></li></ul><p>→shortening of myofibrils → shortening of muscle cell → muscle contraction</p>
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cross-bridge cycle

  1. each myosin head binds to an exposed active site on the actin filament, forming a cross bridge

  2. powerstroke: after cross-bridge formation, myosin head undergoes a conformational change, pivoting towards the center of the sarcomere, called a power stroke, which causes the actin filament to slide relative to the myosin filament and pull the thin filament towards the center of the sarcomere

  3. during the power stroke, ADP and inorganic phosphate are released from the myosin head

  4. the myosin head remains bound to the actin filament until a new ATP molecule binds to it

  5. ATP binds, causing the myosin head to detach from the actin filament

  6. binding of ATP provides energy necessary for myosin head to return to its high-energy cocked state

<ol><li><p>each myosin head binds to an exposed active site on the actin filament, forming a cross bridge</p></li><li><p>powerstroke: after cross-bridge formation, myosin head undergoes a conformational change, pivoting towards the center of the sarcomere, called a power stroke, which causes the actin filament to slide relative to the myosin filament and pull the thin filament towards the center of the sarcomere</p></li><li><p>during the power stroke, ADP and inorganic phosphate are released from the myosin head</p></li><li><p>the myosin head remains bound to the actin filament until a new ATP molecule binds to it</p></li><li><p>ATP binds, causing the myosin head to detach from the actin filament</p></li><li><p>binding of ATP provides energy necessary for myosin head to return to its high-energy cocked state</p></li></ol>
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Ca2+ dependence of cross-bridge attachment

in relaxed muscle: the myosin/actin interaction is inhibited; tropomyosin lies in the grooves of the actin filaments → cross-bridge attachments are blocked

in stimulated muscle: active cross-bridge cycling causes muscle to contract; Ca2+ binds to troponin → tropomyosin moves → cross-bridge attachments can occur

<p>in relaxed muscle: the myosin/actin interaction is inhibited; tropomyosin lies in the grooves of the actin filaments → cross-bridge attachments are blocked</p><p>in stimulated muscle: active cross-bridge cycling causes muscle to contract; Ca2+ binds to troponin → tropomyosin moves → cross-bridge attachments can occur</p>
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twitch

the response of a muscle to a single action potential

↑ action potential frequency → summation of muscle response

<p>the response of a muscle to a single action potential</p><p>↑ action potential frequency → summation of muscle response</p>
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skeletal muscle behavior

contraction strength increases as:

  • more motor units are recruited

  • number of myofibrils increases

  • frequency of stimulation increases

  • myofibril thickness increases

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aerobic vs anaerobic ATP

aerobic ATP production:

  • during low to moderate intensity, sustained activities

  • dominant energy system for activities lasting several minutes or longer/endurance exercises (long distance running, cycling, swimming)

  • processL with oxygen present, glucose or fatty acids are metabolized in the mitochondria through glycolysis, krebs cycle, and ETC

anaerobic ATP production:

  • during high-intensity, short-duration activities where atp demand is very high

  • without oxygen, glucose broken down into pyruvate, converted to lactate which can lead to muscle fatigue

<p>aerobic ATP production:</p><ul><li><p>during low to moderate intensity, sustained activities</p></li><li><p>dominant energy system for activities lasting several minutes or longer/endurance exercises (long distance running, cycling, swimming)</p></li><li><p>processL with oxygen present, glucose or fatty acids are metabolized in the mitochondria through glycolysis, krebs cycle, and ETC</p></li></ul><p>anaerobic ATP production:</p><ul><li><p>during high-intensity, short-duration activities where atp demand is very high</p></li><li><p>without oxygen, glucose broken down into pyruvate, converted to lactate which can lead to muscle fatigue</p></li></ul>
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