The document discusses the anatomy and physiology of three types of muscle tissue: skeletal, cardiac, and smooth muscle. It describes the microscopic structure of muscle fibers and cells, including myofibrils, sarcomeres, and associated proteins. The mechanisms of muscle contraction and relaxation are also explained.
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BBT221 Lecture 7
The document discusses the anatomy and physiology of three types of muscle tissue: skeletal, cardiac, and smooth muscle. It describes the microscopic structure of muscle fibers and cells, including myofibrils, sarcomeres, and associated proteins. The mechanisms of muscle contraction and relaxation are also explained.
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MUSCULAR SYSTEM
• Muscle contraction is a cellular
phenomenon. • Universal Characteristics of Muscle: PHYSIOLOGY • excitability - responds to stimuli (e.g., OF MUSCLE nervous impulses)
CELLS • Conductivity-ability to produce local effect
• contractility - able to shorten in length • extensibility - stretches when pulled • elasticity - tends to return to original shape & length after contraction or extension CLASSIFICATION OF MUSCLE TISSUE • Skeletal muscle may be defined as voluntary striated muscle that is usually attached to one or more bones. • Sk Muscle cells = muscle/myofibers SKELETAL MUSCLE • The Endomysium that surrounds each muscle fiber, the Perimysium that bundles muscle fibers together into fascicles, and the Epimysium that encloses the entire muscle. SKELETAL MUSCLE MICROSCOPIC ANATOMY •Sarcoplasmic reticulum - surround myofibrils longitudinally • Ca2+ reservoir MUSCLE FIBERS Muscle Fibers MYOFIBRILS
Consist of 3 types of myofilaments:
1. Thick filaments – 300 myosin molecules • two peptide chains with globular heads – form cross bridges b/t thick and thin filaments • heads have actin binding sites and ATPase enzymes
2.Thin filaments • actin strands (2) contain binding sites for myosin heads • tropomyosin strands block these sites in relaxed muscles • troponin complex binds to actin, tropomyosin, and calcium
3. Elastic filaments (titin)
• attaches thick filaments to Z disc; holds thick filaments in place; prevents muscle cell from overstretching Dystrophin – accessory protein links thick filaments STRIATIONS AND SARCOMERES A band: Dark band formed by parallel thick filaments that partly overlap the thin filaments (all three myofilaments) H band: A lighter region in the middle of an A band that contains STRIATIONS thick filaments only; thin filaments do not reach this far into the A band in relaxed muscle AND SARCOMERES M line: A dark line in the middle of an H band; meshwork of proteins which anchor thick filaments, origin of the thick filaments I band: A light band composed of thin filaments only, also elastic filaments Z disc: A protein disc to which thin filaments and elastic filaments are anchored at each end of a sarcomere; appears as a narrow dark line in the middle of the I band, anchors thin and elastic filaments MOTOR Axons (fibers) of somatic motor neuron UNIT divide as they enter muscle Motor unit = one nerve fiber and all muscle fibers innervated by it each muscle gets at least one motor nerve, wh/ contains hundreds of motor neurons w/ their axons one axon branches to many terminals, each forms junction w/ one muscle fiber muscle fibers in a motor unit spread throughout muscle, not clustered together small vs. large motor units MOTOR UNIT Each fiber ending forms neuromuscular junction (synapse) w/ a muscle fiber at motor end plate synaptic cleft axonal ending has synaptic vesicles w/ ACh highly folded sarcolemma of motor end plate has receptors for ACh (also ion NEUROMUSCULA channels) R JUNCTION Nerve impulse reaches end of axon→ voltage- gated Ca2+ channels open → Ca2+ influx causes vesicles to fuse w/axon membrane → ACh released ACh binds to receptors on sarcolemma →triggers depolarizationaction potential Acetylcholinesterase on sarcolemma breaks down ACh, prevents continued muscle contraction 1. Recall resting membrane potential: 2. Binding of ACh opens chemically gated ion channels; Na+ gate opens, Na+ in causes depolarization at motor end plate (end-plate potential) GENERATION 3. Voltage-gated channels on sarcolemma OF ACTION next to end plate open, create action POTENTIAL potential that propagates along memb 4. Immediately Na+ gates close and K+ gates open, K+ rushes out and makes inside neg. again (repolarization). Action potential moves down T tubule in triad Terminal cisternae of SR release Ca2+ into sarcoplasm via voltage-gated channels Ca2+ binds to troponin which shifts tropomyosin Binding sites on actin exposed to myosin heads
EXCITATION- ATP bound to myosin heads hydrolyzed which
CONTRACTION activates myosin head COUPLING Myosin heads attach and pull thin filaments toward center of sarcomere ATP binding to head releases it, hydrolysis of ATP cocks head for another stroke, etc. Active transport of Ca2+ back to SR causes restoration of blocking action by troponin, and muscle cell relaxes SLIDING FILAMENT CONTRACTION MODEL
A. thin filaments slide past thick filaments to
overlap to a greater extent than when relaxed B. nerve impulse →myosin heads attach to actin in thin filaments → thin filaments move to center of sarcomere, repeats w/ ATP C. Z bands become closer together, I bands shorten, H zone disappears, muscle fiber shortens Cross-Bridge cycle SMOOTH MUSCLE
Each smooth muscle fiber is a spindle-shaped cell with a diameter
ranging from 2 to 10 µm Smooth muscle fibers have a single nucleus
Two types of filaments
Thick myosin-containing filaments Thin actin-containing filaments. Does not contain sarcomeres. Contains > content of actin than myosin (ratio of 16:1). SMOOTH MUSCLE CONTRACTION
• Depends on rise in free intracellular
Ca2+. • Ca2+ binds with calmodulin. • Ca2+ calmodulin complex joins with and activates myosin light chain kinase. • Myosin heads are phosphorylated. • Myosin heads binds with actin. • Relaxation occurs when Ca2+ concentration decreases.