1 / 80

Skeletal Muscle 骨骼肌

Skeletal Muscle 骨骼肌. Qiang XIA ( 夏强 ), PhD Department of Physiology Room C518, Block C, Research Building, School of Medicine Tel: 88208252 Email: xiaqiang@zju.edu.cn. Muscle. Types of muscle: Skeletal muscle 骨骼肌 Cardiac muscle 心肌 Smooth muscle 平滑肌. Striated muscle 横纹肌.

odysseus-sheppard
Download Presentation

Skeletal Muscle 骨骼肌

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Skeletal Muscle 骨骼肌 Qiang XIA (夏强), PhD Department of Physiology Room C518, Block C, Research Building, School of Medicine Tel: 88208252 Email: xiaqiang@zju.edu.cn

  2. Muscle Types of muscle: • Skeletal muscle骨骼肌 • Cardiac muscle 心肌 • Smooth muscle平滑肌 Striated muscle 横纹肌

  3. Muscle (cont.) • The sliding filament mechanism（肌丝滑行机制）, in which myosin（肌凝蛋白） filaments bind to and move actin （肌纤蛋白）filaments, is the basis for shortening of stimulated skeletal, smooth, and cardiac muscles. • In all three types of muscle, myosin and actin interactions are regulated by the availability of calcium ions. • Changes in the membrane potential of muscles are linked to internal changes in calcium release (and contraction).

  4. Muscle (cont.) • Neuronal influences on the contraction of muscles is affected when neural activity causes changes in themembrane potential of muscles. • Smooth muscles operate in a wide variety of involuntaryfunctions such as regulation of blood pressure andmovement of materials in the gut.

  5. Structure of skeletal muscle

  6. Skeletal muscles are attached to the skeleton by tendons. Skeletal muscles typically contain many, many muscle fibers.

  7. The sarcomere（肌小节） is composed of: thick filaments called myosin, anchored in place by titin fibers, and thin filaments called actin, anchored to Z-lines .

  8. A cross section through a sarcomere shows that: • each myosin can interact with 6 actin filaments, and • each actin can interact with 3 myosin filaments.

  9. Sarcomere structures in an electron micrograph.

  10. Filaments

  11. Myosin filament (thick filament)粗肌丝 • Myosin肌凝蛋白

  12. Actin filament (thin filament)细肌丝 • Actin肌纤蛋白 • Tropomyosin原肌凝蛋白 • Troponin肌钙蛋白

  13. Titin肌联蛋白

  14. Sarcotubular system (1) Transverse Tubule横管 (2) Longitudinal Tubule纵管 Sarcoplasmic reticulum肌浆网

  15. Molecular mechanisms of contraction Sliding-filament mechanism

  16. Contraction (shortening): myosin binds to actin, and slides it, pulling the Z-lines closer together, and reducing the width of the I-bands. Note that filament lengths have not changed.

  17. Contraction: myosin’s cross-bridges（横桥） bind to actin; the crossbridges then flex to slide actin.

  18. Click here to play the Sarcomere Shortening Flash Animation

  19. The thick filament called myosin is actually a polymer of myosin molecules, each of which has a flexible cross-bridge that binds ATP and actin.

  20. 4. Partial hydrolysis of the bound ATP energizes or “re-cocks” the bridge. 2. The full hydrolysis and departure of ADP + Picauses the flexing of the bound cross-bridge. 3. Binding of a “new” ATP to the cross-bridge uncouples the bridge. The myosin-binding site on actin becomes available, so the energized cross-bridge binds. 1. The cross-bridge cycle requires ATP

  21. The myosin-binding site on actin becomes available, so the energized cross-bridge binds. 1.

  22. 2. The full hydrolysis and departure of ADP + Picauses the flexing of the bound cross-bridge.

  23. 3. Binding of a “new” ATP to the cross-bridge uncouples the bridge.

  24. 4. Partial hydrolysis of the bound ATP energizes or “re-cocks” the bridge.

  25. 4. Partial hydrolysis of the bound ATP energizes or “re-cocks” the bridge. 2. The full hydrolysis and departure of ADP + Picauses the flexing of the bound cross-bridge. 3. Binding of a “new” ATP to the cross-bridge uncouples the bridge. The myosin-binding site on actin becomes available, so the energized cross-bridge binds. 1. The cross-bridge cycle requires ATP

  26. Click here to play the Cross-bridge cycle Flash Animation

  27. Roles of troponin, tropomyosin, and calcium in contraction In relaxed skeletal muscle, tropomyosin blocks the cross-bridge binding site on actin. Contraction occurs when calcium ions bind to troponin; this complex then pulls tropomyosin away from the cross-bridge binding site.

  28. Interaction of myosin and actin

  29. Excitation-contraction coupling 兴奋-收缩偶联 • Transmission of action potential (AP) along T tubules • Calcium release caused by T tubule AP • Contraction initiated by calcium ions

  30. The latent period between excitation and development of tension in a skeletal muscle includes the time needed to release Ca++ from sarcoplasmic reticulum, move tropomyosin, and cycle the cross-bridges.

  31. The transverse tubules bring action potentials into the interior of the skeletal muscle fibers, so that the wave of depolarization passes close to the sarcoplasmic reticulum, stimulating the release of calcium ions. The extensive meshwork of sarcoplasmic reticulum assures that when it releases calcium ions they can readily diffuse to all of the troponin sites.

  32. Passage of an action potential along the transverse tubule opens nearby voltage-gated calcium channels, the “ryanodine receptor,” located on the sarcoplasmic reticulum, and calcium ions released into the cytosol bind to troponin. The calcium-troponin complex “pulls” tropomyosin off the myosin-binding site of actin, thus allowing the binding of the cross-bridge, followed by its flexing to slide the actin filament.

  33. Which of these following proteins contains the binding sites for Ca2+ that initiates contraction? A Myosin B Troponin I C Tropomyosin D Troponin C E Troponin T

  34. General process of excitation and contraction in skeletal muscle • Neuromuscular transmission • Excitation-contraction coupling • Muscle contraction

  35. A single motor unit（运动单位） consists of a motor neuron and all of the muscle fibers it controls.

  36. The neuromuscular junction（神经肌接头）is the point of synaptic contact between the axon terminal of a motor neuron and the muscle fiber it controls. Action potentials in the motor neuron cause Acetylcholine（乙酰胆碱） release into the neuromuscular junction. Muscle contraction follows the delivery of acetylcholine to the muscle fiber.

  37. 1. The exocytosis of acetylcholine from the axon terminal occurs when the acetylcholine vesicles merge into the membrane covering the terminal. 2. On the membrane of the muscle fiber, the receptors for acetylcholine respond to its binding by increasing Na+ entry into the fiber, causing a graded depolarization. 3. The graded depolarization typically exceeds threshold for the nearby voltage-gate Na+ and K+ channels, so an action potential occurs on the muscle fiber.

  38. Nicotinic acetylcholine receptor 烟碱型乙酰胆碱受体 Acetylcholinesterase 乙酰胆碱酯酶

  39. End plate potential (EPP) 终板电位

  40. Miniature end plate potential 微终板电位 • Small fluctuations (typically 0.5 mV) in the resting potential of postsynaptic cells. • They are the same shape as, but much smaller than, the end plate potentials caused by stimulation of the presynaptic cell. Miniature end plate potentials are considered as evidence for the quantal release of neurotransmitters at chemical synapses, a single miniature end plate potential resulting from the release of the contents of a single synaptic vesicle.

  41. Click here to play the Neuromuscular Junction Flash Animation

  42. Click here to play the Action Potentials and Muscle Contraction Flash Animation

  43. A woman comes to your clinic and explains that she is noting gradually worsening fatigue/weakness in her legs when she goes for her walk. She also mentions a droopy right eyelid, and wonders if this is a normal aging process. You examine her and find the following: overall decreased muscle strength, trace reflexes throughout, and weakness of eyelid closure bilaterally. The rest of the exam is unremarkable. What would you administer to treat the likely condition? A Muscarinic blockers B Nicotinic blockers C Acetylcholinesterase blockers D Alpha blockers E Beta blockers

  44. Neuromuscular transmission A Is caused by the release of acetylcholine from the muscle side of the junction B Shows a permeability change to Na+ and K+ at the receptor site during the endplate potential (EPP) C May be facilitated by curare in myasthenia gravis D Is blocked by curare because it competes with the Na+ entry during the muscle action potential E Is solely an electronic function

  45. A miniature end-plate potential is A Not related to changes in ionic permeability B A reduced action potential in the motor end-plate C Produced by spontaneous release of acetylcholine D Responsible for weak muscular contractions E An afterdischarge at the neuromuscular junction

  46. The action of acetylcholine at the neuromuscular junction is terminated primarily by A Enzymatic breakdown by choline acetylase B Enzymatic breakdown by acetylcholinesterase C Uptake into the muscle D Uptake into the nerve ending E Diffusion into the surrounding extracellular fluid

  47. The transmission of an action potential over the muscle fiber membrane causes the contraction of the fiber a few milliseconds later. Which of the following terms is used to describe that process? A Ratchet Theory of Muscle Contraction B Excitation Contraction Coupling C Membrane Potential D All-or -Nothing Law

More Related