Week 9 - Muscle Microanatomy/Histology

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key terms and concepts

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<p>Key Characteristics of Skeletal Muscle</p>

Key Characteristics of Skeletal Muscle

  • Voluntary movement

  • Multi-nucleated

  • Straited

  • Vascularized

  • Innervated by a plexus (network of blood vessels and nerves)

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The Layers of Fascia

  • epimysium: surrounds the entire muscle

  • perimysium: surrounds a bundle of muscle fibers (fascicle)

  • endomysium: surrounds a single muscle fiber

<ul><li><p>epimysium: surrounds the entire muscle</p></li><li><p>perimysium: surrounds a bundle of muscle fibers (fascicle)</p></li><li><p>endomysium: surrounds a single muscle fiber</p></li></ul><p></p>
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What makes up a muscle? (superficial to deep)

fascicle, muscle fiber, myofibrils, sarcomere, actin & myosin

<p>fascicle, muscle fiber, myofibrils, sarcomere, actin &amp; myosin</p>
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What is the structure of a sarcomere?

  • Z-Disc (Z-Line): Zigzag lines marking the boundaries of a sarcomere, anchoring the thin (actin) filaments.

  • A-Band (Anisotropic): The dark band, spanning the entire length of the thick (myosin) filaments, including overlapping thin filaments. Its length remains constant during contraction.

  • I-Band (Isotropic): The lighter region containing only thin (actin) filaments, bisected by the Z-disc. It shortens during contraction.

  • H-Zone: The pale area in the center of the A-band containing only thick (myosin) filaments (no thin filament overlap). It shrinks or disappears during contraction.

  • M-Line (Midline): A dark line in the very center of the H-zone, where myosin filaments are linked. 

    • The I band and H zone shorten when a muscle contracts.

<ul><li><p><span><strong><span>Z-Disc (Z-Line):</span></strong><span> Zigzag lines marking the boundaries of a sarcomere, anchoring the thin (actin) filaments.</span></span></p></li><li><p><span><strong><span>A-Band (Anisotropic):</span></strong><span> The dark band, spanning the entire length of the thick (myosin) filaments, including overlapping thin filaments. Its length remains constant during contraction.</span></span></p></li><li><p><span><strong><span>I-Band (Isotropic):</span></strong><span> The lighter region containing </span><em><span>only</span></em><span> thin (actin) filaments, bisected by the Z-disc. It shortens during contraction.</span></span></p></li><li><p><span><strong><span>H-Zone:</span></strong><span> The pale area in the center of the A-band containing </span><em><span>only</span></em><span> thick (myosin) filaments (no thin filament overlap). It shrinks or disappears during contraction.</span></span></p></li><li><p><span><strong><span>M-Line (Midline):</span></strong><span> A dark line in the very center of the H-zone, where myosin filaments are linked.&nbsp;</span></span></p><ul><li><p>The I band and H zone shorten when a muscle contracts.</p></li></ul></li></ul><p></p>
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Excitation-contraction coupling

  1. Neural Stimulation: A motor neuron releases acetylcholine (ACh) at the neuromuscular junction, generating an action potential on the muscle's sarcolemma (cell membrane).

  2. Signal Propagation: The action potential travels along the sarcolemma and into the T-tubules (deep invaginations of the membrane).

  3. Calcium Release: The electrical signal activates voltage-sensitive Dihydropyridine Receptors (DHPRs) in the T-tubules, which are physically linked to Ryanodine Receptors (RyRs) on the SR. This interaction pulls open the RyRs, releasing stored Ca2+ into the sarcoplasm (cytoplasm).

  4. Cross-Bridge Cycling: The increased intracellular Ca2+ binds to troponin, causing tropomyosin to shift and uncover myosin-binding sites on actin.

  5. Muscle Contraction: Myosin heads bind to actin, forming cross-bridges, and perform the power stroke, pulling the thin filaments towards the sarcomere's center, causing muscle shortening (contraction).

  6. Relaxation: When the nerve signal stops, Ca2+ is actively pumped back into the SR, tropomyosin covers the binding sites, and the muscle relaxes. 

<ol><li><p><span><strong><span>Neural Stimulation</span></strong><span>: A motor neuron releases acetylcholine (ACh) at the neuromuscular junction, generating an action potential on the muscle's sarcolemma (cell membrane).</span></span></p></li><li><p><span><strong><span>Signal Propagation</span></strong><span>: The action potential travels along the sarcolemma and into the T-tubules (deep invaginations of the membrane).</span></span></p></li><li><p><span><strong><span>Calcium Release</span></strong><span>: The electrical signal activates voltage-sensitive Dihydropyridine Receptors (DHPRs) in the T-tubules, which are physically linked to Ryanodine Receptors (RyRs) on the SR. This interaction pulls open the RyRs, releasing stored Ca2+ into the sarcoplasm (cytoplasm).</span></span></p></li><li><p><span><strong><span>Cross-Bridge Cycling</span></strong><span>: The increased intracellular Ca2+ binds to troponin, causing tropomyosin to shift and uncover myosin-binding sites on actin.</span></span></p></li><li><p><span><strong><span>Muscle Contraction</span></strong><span>: Myosin heads bind to actin, forming cross-bridges, and perform the power stroke, pulling the thin filaments towards the sarcomere's center, causing muscle shortening (contraction).</span></span></p></li><li><p><span><strong><span>Relaxation</span></strong><span>: When the nerve signal stops, Ca2+ is actively pumped back into the SR, tropomyosin covers the binding sites, and the muscle relaxes.&nbsp;</span></span></p></li></ol><p></p>
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Where is smooth muscle found?

walls of hollow visceral organs (stomach, bladder)

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What are the key characteristics of smooth muscle

non-striated, involuntary, mono nucleated

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Types of contractions produced by smooth muscle

slow and smooth, peristalsis (contraction, relax, repeat)

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Where is cardiac muscle found?

only in the myocardium (wall of the heart)

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The key characteristics of cardiac muscle

striated, involuntary, mononucleated

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How does cardiac muscle contract?

  • automaticity; action potential created spontaneously by the heart

  • intercalated discs (gap junctions) spread action potentials throughout heart, causing rhythmic contractions of the heart