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Chapter 9 Types of Muscle Tissue Derived from mesoderm Skeletal Skeletal, striated, voluntary, multinucleated Fast, fatigued contractions Adaptable (paperclip vs textbook) Smooth Visceral, nonstriated, involuntary, uninucleated Slow, sustained contractions Cardiac Cardiac, striated, involuntary, uninucleated Contraction rate stabilized by pacemaker cells Neural control can alter Intercalated discs Functional Characteristics Excitability Receive and respond to a stimulus (pH or NT) Electrical impulse along the sarcolemma Contractibility Shorten and thicken w/ appropriate stimulation Extensibility Stretch or extend without damage Elasticity Return to normal shape after a stretch Muscle Function Produce movement Sk: locomotion, manipulation, and response Sm: squeeze substances through Car: keep blood moving Maintain posture and position Adjustments to stay erect or seated despite gravity Protection Encloses viscera and forms valves (control) Generate heat Contractions keep body temp at 98.6 Stabilize joints Pull on bones for movement, but strengthen joints Gross Anatomy of Skeletal Muscle Discrete organs of all 4 tissue types Nerves and blood 1 nerve, 1 artery, & 1+ vein per muscle Enter centrally; 1 nerve ending per muscle fiber (cell) Constant O2 and nutrients b/c contractions are high E demand Connective tissue Support and reinforce 3 layers (internal to external) Endomysium: cover muscle fiber Perimysium: cover fasicle Epimysium: cover muscle Attachments Direct: epimysium fused to periosteum Indirect: epimysium beyond muscle = tendon Microscopic Anatomy Sarcolemma Sacroplasm Glycogen, myoglobin, and mitochondria Myofibrils Actin (thin) and myosin (thick) proteins arranged into repeating sarcomeres Sarcoplasmic reticulum (SR) Smooth ER surrounding myofibrils Triads Terminal cisternae SR is enlarged and joins with T tubules; occur in pairs Transverse (T) tubules Deep indentions of sarcolemma into sarcoplasm; conduct Ca2+ into cell Sarcomere Organization Smallest functional unit of skeletal muscle fiber A bands dark b/c contain thick and thin filaments H zone is lighter middle because it lacks thin filaments M line created by a protein that link thick filaments I bands light b/c contain thin filaments only Z line connect thin filaments together in a zig zag pattern Marks end of sarcomere Zone of overlap 6 thin surround 1 thick; 3 thick surround 1 thin Myofilament Structure Thick filaments Bundles of myosin proteins Composed of a rod-like tail and globular head Head forms cross bridges; attach to site on actin; contain ATPases Thin filaments Twisted strands of F actin, composed of G actin G actin contains ‘active sites’ where myosin can attach Tropomyosin forms stiffening chains that cover ‘active sites’ Troponin holds the tropomyosin in place Changes shape to expose active sites G-actin = pearl, F-actin = strand, tropomysin = strands together Sliding Filament Theory During contraction, sarcomeres (not filaments) shorten Z lines closer, shortening sarcomere H band and I band narrow Zone of overlap increases A band doesn’t change Sliding Mechanism Cross bridges detached Tropomyosin blocks ‘active sites’ Active site exposed cross bridge attach Ca2+ binds troponin shape change Myosin head pivots toward M line thin filaments to center Cross bridges detach and mysoin reactivated ATP binds ATPase resets Neuromuscular Junction (NMJ) Innervation of muscle fiber by an axon terminal 1 NMJ per muscle fiber Motor unit: motor neuron and all muscle fibers innervated Fewer fibers = more precise Number determines strength of muscle Separated by a synaptic cleft Axon terminal houses synaptic vesicles filled with acetylcholine (Ach) Impulse opens Ca2+ channels to http://www.colorado.edu/intphys/Class/IPHY3430-200/image/figure7m.jpg release Motor end plate is depression in the sarcolemma for the axon Contains Ach receptors Propogates an action potential (AP) Introduction to Action Potentials Resting membrane is polarized (charge separation) NT binds = opens gated ion channels (Na + and K +) Depolarize cell (less ‘–’ or more ‘+’) locally Spreads throughout plasma membrane in waves Initiates AP Adjacent Na + open more depolarization to threshold Na + close, K + open = repolarization Refractory period because no stimuli can initiate Resets electrical condition to resting state Na + /K + pump restore ionic condition All or none response, b/c unstoppable once started Excitation – Contraction Coupling Stimuli releases ACh, depolarizes end plate AP propagated down T tubules Termianl cisternae of SR release Ca 2+ Electrical signal raise Ca2+ levels by opening Ca2+ channels Ca2+ binds troponin, removing tropomyosin block Contraction occurs (see earlier) Ca2+ levels decrease, tropomyosin replaced = relaxation ATP dependent Ca2+ pump into SR Repeat with stimulation Skeletal Muscle Contractions Muscle Tone Alternating active motor units while muscle at rest No active movements produced Stabilize joints and maintain posture Ensure response ready Isotonic Tension constant as muscle length changes Isometric Tension increases to peak, but muscle length unchanged Moving a load greater than developable tension Concentric : force w/shortening Eccentric : force w/lengthening (gastrocnemius & hills) Muscle Twitch Response to a single stimulation Quick contract, relax cycle in 3 phases Latent period Excitation – coupling is occurring Muscle tension increases, but no contraction Contraction period Cross bridges active Peak tension, muscle shortens Relaxation period Reentry Ca2+ into SR Muscle tension to zero, resting Varies between muscle types Strength depends on # of motor units, recruitment Graded Muscle Responses Contraction varies depending on circumstance Wave summation (time) 2 stimuli in rapid succession = larger contraction 2nd time Refractory period unaltered Tetanus (speed) Sustained contraction w/ or w/o partial relaxation Unfused Fused Treppe Increase tension with repeated contractions Warming up stronger later to same stimulus Muscle Metabolism Muscle Disorders Myasthenia gravis: autoimmune disease, loss of Ach receptors Rigor mortis: ATP depletion prevents cross bridge detachment Atrophy: degeneration of muscle from disuse Duchenne muscular dystrophy: sex-linked disease that destroys muscle Hernia: organ protrudes through abdominal wall Myalgia: muscle pain Fibromyositis: inflammation of a muscle and CT coverings Strain: excessive stretching and tearing of muscle or tendon