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42 Cards in this Set
- Front
- Back
locomotion
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movement of the body
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excitable
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nervous tissue and muscle tissue
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action potential
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electrical impulses that (in this case) cause contraction
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extensible
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muscle tissue can stretch
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elasticity
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muscle tissue can recoil back to original shape and size
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Muscle tissue is
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elastic
extensible excitable |
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Epimysium
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covering of skeletal muscle organ as a whole
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Perimysium
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the connective tissue between each muscle fascicle
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Endomysium
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the connective tissue between each muscle fiber (cell)
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sarcolemma
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cell membrane of a muscle fiber
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sarcoplasm
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the cytoplasm of surrounding individual muscle fiber cells
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T tubules
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connects sarcolemma to interior of muscle fiber
pass contraction stimuli to deeper regions of muscle fiber |
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myofibrils
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thousands of rods of proteininside each muscle fiber
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sarcoplasmic reticulum
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modified endoplasmic reticulum that stores calcium ions
surrounds each myofibril |
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terminal cisternae
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large calcium ion sotrage chambers which lie adjacent to transverse tubules
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triad
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sandwich made of a t-tubule, plus terminal cisterna on either side
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Actin
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THIN filament (3000)
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Myosin
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THICK filament (1500)
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sarcomere
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repeating patterns of actin and myosin along a myofibril
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Z line
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where thin actin connects to one another at the END of a sarcomere
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Actinin
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what makes up a Z line
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I band
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area newar Z line that contains only thin filaments
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A band
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area containing both thin and thick filaments located between I bands in a sarcomere
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zone of overlap
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where thick and thin bind during muscle contraction
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H zone
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middle region of an A band and contains ONLY THICK filaments
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Four proteins that make up actin strands
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G actin
F actin nebulin active sites |
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G actin
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spherical molecules like pearls on a necklace
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F actin
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300-400 G actins twist together
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Nebulin
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"string of a necklace" that holds beads "g-actins" in place
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tropomyosin
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follows twisted actin strands and blocks active sites to regulate muscle contraction
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troponin
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holds tropomyosin in position and has binding sites for calcium ions
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two strands of myosin
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two intertwined tail regions and two globular head regions
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titin
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protein that attaches thick filament to the Z line on end of sarcomere
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Muscular dystrophies
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inherited diseases that cause changes in muscle proteins that result in progressive weakening and deterioration of skeletal muscles
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DMD (Duchenne
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starts in childhood and fatal with cardiac and respiratory failure by age of 20
mutation of gene for muscle protein dystrophin part of anchoring complex that attaches thin filaments to sarcolemma calcium channels remain open in absence of dystrophin located on X chromosome mothers can be carriers and 50% chance to pass on to male offspring |
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motor neuron
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nerve cell controlling skeletal muscle fiber
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ACh
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chemical released by motor neuron
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Neuromuscular junction/ myoneural junction
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where motor neuron and muscle fiber meet
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synaptic vesicles
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store ACh at end of synaptic knob/terminal
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Synaptic cleft
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small gap that separates knob from a folded area of sarcolemma called motor end plate
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AChE
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esterase- breaks down ACh to prevent over stimulation of muscle fiber
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Muscle contraction
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AP travels down neuron and raches synaptic knob and vesicles release ACh into synaptic cleft. ACh diffuses across cleft and binds to ACh receptors embedded in sarcolemma at motor end plate of muscle fiber. Binding causes sarcolemma to generate an action potential. Spread down T tubules causing calcium ions to be released from sarcoplasmic reticulum into sarcoplasm of muscle fiber. Calcium ions bind to troponin which moves tropomyosin and exposes active sites on G actins. Myosin heads attach at active sites and ratchet thin filaments inward. Thin filaments slide into H zone and sarcomere shorterns
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