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Cell Physiolgy By: Dr. Foadoddini Department of Physiology & - PowerPoint PPT Presentation

Chapt. 6,7,8 Cell Physiolgy By: Dr. Foadoddini Department of Physiology & Pharmacology Birjand University of Medical Sciences Dr. Foadoddini Contraction of Skeletal Muscle Dr. Foadoddini Dr. Foadoddini Dr. Foadoddini T


  1. Chapt. 6,7,8 Cell Physiolgy By: Dr. Foadoddini Department of Physiology & Pharmacology Birjand University of Medical Sciences ١ Dr. Foadoddini

  2. Contraction of Skeletal Muscle ٢ Dr. Foadoddini

  3. ٣ Dr. Foadoddini

  4. ٤ Dr. Foadoddini

  5. T ‐ tubule ٥ Dr. Foadoddini

  6. Sliding Filament Mechanism ٦ Dr. Foadoddini

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  13. active tension ١٣ Dr. Foadoddini

  14. Tension N Length ١٤ Dr. Foadoddini

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  16. Energy for: Sliding Ion Pumps Sources of Energy: 1. Phosphocreatine 2. glycolysis" of glycogen 3. Oxida tj ve metabolism Efficiency of Muscle Contraction: ٢۵ % Max at a moderate velocity ١٦ Dr. Foadoddini

  17. muscle twitch: a single, sudden contraction lasting for a fraction of a second. Latency The characteristics of isotonic contraction depend on the load and the inertia of the load. However, the isometric system records strictly changes in force of muscle contraction itself. Therefore, the isometric system is most often used when comparing the functional characteristics of different muscle types. ١٧ Dr. Foadoddini

  18. Fast Versus Slow Muscle Fibers M otor unit: All the muscle fibers innervated by a single nerve fiber . ١٨ Dr. Foadoddini

  19. Force Summation: Multiple fiber summation : ( size principle) are driven asynchronously Thus providing smooth contraction Frequency summation: tetanization The Staircase Effect (Treppe) muscle tone Muscle Fatigue ١٩ Dr. Foadoddini

  20. Coactivation of Antagonit Msuscles Remodeling of Muscle to Match Function Hypertrophy the number of actin and myosin filaments in each muscle fiber Atrophy Hyperplasia actual number of muscle fibers Adjustment of Muscle Length Effects of Muscle Denervation Atrophy, degenerative changes, replaced by fibrous and fatty tissue, contracture ٢٠ Dr. Foadoddini

  21. Excitation of Skeletal Muscle: Neuromuscular Transmission and Excitation-Contraction Coupling ٢١ Dr. Foadoddini

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  24. End- plate potential ٢٤ Dr. Foadoddini

  25. Ca K ٢٥ Dr. Foadoddini

  26. Type of drugs: ٢٦ Dr. Foadoddini

  27. Curar Botulinum ٢٧ Dr. Foadoddini

  28. In Frog muscle Heart ٢٨ Dr. Foadoddini

  29. Calsequestrin Dr. Foadoddini ٢٩

  30. Excitation ‐ Contraction Coupling ٣٠ Dr. Foadoddini

  31. Smooth Dr. Foadoddini Muscle ٣١

  32. mass of hundreds to thousands of smooth muscle fibers that contract together as a single unit. adherent to one another many gap junctions Depolar. Without action potenential but junctional pot .. Syncytial smooth muscle Visceral smooth muscle Control mainly by nerve signals By non-nervous stimuli ciliary muscle , iris muscle of the eye, piloerector gut, bile ducts, ureters, uterus, muscles that cause erection of the hairs many blood vessels. ٣٢ Dr. Foadoddini

  33. dense bodies A/M= 5 to 10/1 Vs, 2/1 in skletal "side polar" cross-bridges So, contract as much as 80 per cent of their length ٣٣ Dr. Foadoddini

  34. Tonic contraction, sometimes lasting hours or even days Slow Cycling of the Myosin Cross-Bridges far less ATPase activity Less Energy Ryequired to Sustained Contraction Slowness Of Onset Contraction and Relaxation Force of Muscle Contraction "Latch“ Mechanism for Prolonge Holding of Contraction of Smooth Muscle Stress- relaxation as the activation of the enzymes decreases, the cycling frequency decreases, allows the myosin heads to remain attached ٣٤ Dr. Foadoddini

  35. Cross-bridge activation in smooth muscle Ca 2+ -stimulated myosin phosphorylation 4 Ca 2+ myosin light Ca Cm 4 chain kinase (MLCK) Calmodulin, Cm myosin light Ca Cm 4 chain kinase Mg 2+ ATP ADP regulatory P light chain relaxation contraction myosin P phosphatase ٣٥ Dr. Foadoddini

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  38. Smooth muscle can maintain force with reduced energy expenditure Smooth muscle has the ability to maintain force development even when a high [Ca 2+ ] and hence cross-bridge turnover is not maintained. Maintained force development, but with reduced velocity of movement, confers a clear physiological advantage to smooth muscle and is absent from striated muscle. [Ca 2+ ] force velocity & crossbridge phosphorylation stimulation ٣٨ Dr. Foadoddini

  39. contact junctions diffuse junctions Excitatory and Inhibitory Transmitter Substances Ach NE Type of receptor ٣٩ Dr. Foadoddini

  40. slow wave rhythm pacemaker waves self-excitatory voltage-gated calcium channels Excitation of Visceral Smooth Muscle by Muscle Stretch Excitation or Inhibition Hormones and Local Tissue Factor ٤٠ Dr. Foadoddini

  41. ٤١ Dr. Foadoddini

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