- Dr. Foadoddini
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Cell Physiolgy
By: Dr. Foadoddini
Department of Physiology & Pharmacology Birjand University of Medical Sciences
- Chapt. 6,7,8
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
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By: Dr. Foadoddini
Department of Physiology & Pharmacology Birjand University of Medical Sciences
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T‐ tubule
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Sliding Filament Mechanism
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active tension
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Tension Length N
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Energy for: Sliding Ion Pumps Sources of Energy:
Efficiency of Muscle Contraction: ٢۵% Max at a moderate velocity
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muscle twitch: a single, sudden contraction lasting for a fraction of a second. 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.
Latency
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Fast Versus Slow Muscle Fibers Motor unit: All the muscle fibers innervated by a single nerve fiber .
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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
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Coactivation
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 Effects of Muscle Denervation Atrophy, degenerative changes, replaced by fibrous and fatty tissue, contracture
Adjustment of Muscle Length
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Excitation of Skeletal Muscle: Neuromuscular Transmission and Excitation-Contraction Coupling
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End- plate potential
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Ca K
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Type of drugs:
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Curar Botulinum
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In Frog muscle Heart
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Calsequestrin
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Excitation‐Contraction Coupling
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Syncytial smooth muscle Visceral smooth muscle
gut, bile ducts, ureters, uterus, many blood vessels. mass of hundreds to thousands of smooth muscle fibers that contract together as a single unit. adherent to one another many gap junctions ciliary muscle , iris muscle of the eye, piloerector muscles that cause erection of the hairs
Control mainly by nerve signals By non-nervous stimuli
but junctional pot..
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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
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Stress- relaxation "Latch“ Mechanism for Prolonge Holding of Contraction of Smooth Muscle 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 as the activation of the enzymes decreases, the cycling frequency decreases, allows the myosin heads to remain attached
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P
myosin light chain kinase Ca Cm 4
ATP ADP
Mg2+
myosin phosphatase P
myosin light chain kinase (MLCK) Ca Cm 4 4 Ca2+ Calmodulin, Cm
contraction
relaxation
regulatory light chain
Cross-bridge activation in smooth muscle
Ca2+-stimulated myosin phosphorylation
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Smooth muscle can maintain force with reduced energy expenditure
stimulation force [Ca2+] velocity & crossbridge phosphorylation Smooth muscle has the ability to maintain force development even when a high [Ca2+] 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.
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diffuse junctions contact junctions Excitatory and Inhibitory Transmitter Substances Ach NE Type of receptor
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slow wave rhythm pacemaker waves
Excitation of Visceral Smooth Muscle by Muscle Stretch
voltage-gated calcium channels self-excitatory
Excitation or Inhibition Hormones and Local Tissue Factor
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