Skeletal Muscle Mechanics About Disease.co. 7. Isotonic vs. isometric contraction.
Molecular Basis of Skeletal Muscle Contraction
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Transcript of Molecular Basis of Skeletal Muscle Contraction
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Molecular Basis of Skeletal Muscle Contraction
Dr.Mohammed Sharique Ahmed QuadriAssistant Professor
Department Basic Medical Sciences Division of Physiology Faculty of Medicine Almaarefa Colleges
بسم الله الرحمن الرحيم
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ObjectivesBy the end of this lecture, you should be able to:
Understand the Molecular mechanism of skeletal muscle contraction including:
Role of calcium ions in excitation contraction coupling
Sliding Filament Theory of Contraction The role of T-tubule and sarcoplasmic
reticulum Regulation of Calcium efflux and influx from
the sarcoplasmic reticulum and into the sarcoplasm
Molecular rearrangement of Actin and Myosin Myosin-ATPase cycle and Rigor Mortis
phenomenon
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Structure and Arrangement of Myosin Molecules Within Thick Filament
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Role of Calcium in Cross-Bridge Formation
• During relaxed state
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Role of Calcium in Cross-Bridge Formation
• Excited
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Sliding Filament Mechanism
Cross-bridge interaction between actin and myosin brings about muscle contraction by means of the sliding filament mechanism.
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Sliding Filament Mechanism
• Increase in Ca2+ starts filament sliding• Decrease in Ca2+ turns off sliding process• Thin filaments on each side of sarcomere slide
inward over stationary thick filaments toward center of A band during contraction
• As thin filaments slide inward, they pull Z lines closer together
• Sarcomere shortens
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Sliding Filament Mechanism
• All sarcomeres throughout muscle fiber’s length shorten simultaneously
• Contraction is accomplished by thin filaments from opposite sides of each sarcomere sliding closer together between thick filaments.
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Changes in Banding Pattern During Shortening
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Power Stroke• Activated cross bridge bends toward center of
thick filament, “rowing” in thin filament to which it is attached– Sarcoplasmic reticulum releases Ca2+ – Myosin heads bind to actin– Hydrolysis of ATP transfers energy to myosin head
and reorients it– Myosin heads swivel toward center of sarcomere
(power stroke)– ATP binds to myosin head and detaches it from
actin
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Relaxation
• Depends on reuptake of Ca2+ into sarcoplasmic reticulum (SR)
• Acetylcholinesterase breaks down ACh at neuromuscular junction
• Muscle fiber action potential stops • When local action potential is no longer
present, Ca2+ moves back into sarcoplasmic reticulum
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Excitation contraction couplingT Tubules and Sarcoplasmic Reticulum
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Relationship Between T Tubule and Adjacent Lateral Sacs of Sarcoplasmic Reticulum
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Calcium Release in Excitation-Contraction Coupling
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CROSS-BRIDGE CYCLE
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Contraction-Relaxation Steps Requiring ATP
• Splitting of ATP by myosin ATPase provides energy for power stroke of cross bridge
• Binding of fresh molecule of ATP to myosin lets bridge detach from actin filament at end of power stroke so cycle can be repeated
• Active transport of Ca2+ back into sarcoplasmic reticulum during relaxation depends on energy derived from breakdown of ATP
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References
• Human physiology by Lauralee Sherwood, 7th edition
• Text book physiology by Guyton &Hall,12th edition
• Text book of physiology by Linda .s contanzo,third edition
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