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anatomy and physiology of muscle

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Diseases related to muscle physiology   Sarcopenia- age related loss of muscle Diabetes (1 and 2)- skeletal muscle removes glucose from blood Cardiovascular disease- heart; Cardiac hypertrophy deals with cardiac muscle; Coronary artery disease deals with smooth muscle  
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Basic muscle function   turns chemical energy into mechanical force  
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Functional characteristics of muscle   1.Excitability or irritability 2. Contractibility 3.Extensibility 4.Elasticity  
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Excitability or irritability   the ability to receive and respond to stimuli (depolarization)  
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Contractibility   the ability to shorten forcibly  
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Extensibility   the ability to be stretched or extended  
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Elasticity   The ability to recoil and resume the original resting length  
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3 types of muscle   1.Skeletal-striated and multi-nucleated; voluntary 2.Cardiac- striated and multi-nucleated; involuntary 3.Smooth- not striated and single nuclei for each cell; involuntary  
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Skeletal muscle   multiple nuclei; regular banding patterns that are organized by contractile proteins  
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Skeletal muscle development   muscle arises from the mesoderm; myoblast; multi-nucleated myotube; myofiber  
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Myoblast   muscle cell, fused together  
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multi-nucleated myotube   myoblasts fused together no longer have mitotic abilities; instead we alter size (weight lifting) by adding or subtracting nuclei by adding satellite cells (cells floating outside myotube)  
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Myofiber   smalles complete contractile system; activated when nerve hits myotube but if nerve fails to make contact the myotube will wither and die  
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Structure of skeletal muscle   1.Epimysium 2.Fascicle 3.Fibers 4.Myofibril 5.Sarcomere 6.Perimysium 7.Endomysium 8.Sarcolemma  
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Epimysium   Layer of connective tissue outside muscle that covers the entire thing; dense irregular connective tissue  
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Fascicle   a bundle of muscle fibers wrapped in perimysium; contains smaller bundles of muscle fibers  
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Perimysium   A layer of connective tissue that wraps muscle fibers into bundles or fascicles; dense irregular tissue  
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Fibers   Formed by the fusion of myoblasts; a long, cylinder, multi-nucleated cell; nuclei is under sarcolemma and has other cell organelles like mitochondria; each fiber is wrapped in endomyseum  
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Endomysium   Areolar connective tissue; layer of connective tissue that surrounds muscle fibers  
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Sarcolemma   The plasma membrane of a muscle cell (muscle fiber)  
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Myofibril   The basic unit of a muscle; Where contraction takes place; a long strand of sarcomeres; found in the skeletal muscle fibers; held together in a long chain by proteins and organized into myofiliments  
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Sarcomere   Smallest functional unit of skeletal muscle; Shortens for muscle contraction; runs Z-disc to Z-disc; composed to thick filaments-Myosin and thin filaments- Actin (slide past each other to contract)  
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Overview of skeletal muscle contraction   Myosin binds to actin to shorten; myosin heads work with receptor proteins of actin  
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Muscle striations   made by sarcomeres; striations consist of A-bands, I-bands, M-lines, and H-zones  
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A-band   Anisotropic- light does not pass through due to high concentration of protein; Dark area  
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I-band   Isotropic- light can pass through due to less protein; light area  
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M-line   Dark band in the center of the sarcomere; consists of proteins that anchor thick filaments to the center of the sarcomere  
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H-zones   Light bands that are located on either side of the M-line  
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I-band (blue circles)   6 actin form a circle; thin filaments (actin) molecules only  
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H-zone (red circles)   Thick filaments (myosin) molecules only  
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M-line (red circles connected)   proteins connect thick filaments (myosin) only; do not connect think filaments at all  
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A-band (blue and red circles)   thick and then filaments (actin and myosin); 6 thin filaments for every thick filament  
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Thick filaments (myosin) structure   Globular myosin head- binds to actin; tails- are intertwined that interact with other myosin subunits and regulate motor activity; neck- acts as a lever (hinges to change shape)  
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Thin filaments (actin) structure   long chains made of actin molecules (twisted); each actin has a myosin binding site; protein strands run through actin filament called tropomyosin; yellow proteins called troponin  
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Tropomyosin   Protein strands; blocks myosin binding site on actin and prevents contraction  
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Troponin complex   Yellow proteins complexes that contain 3 proteins; inhibit tropomyosin to allow binding and contraction when and action potential is created  
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T-Tubules   Part of the plasma membrane of the sarcolemma; studded with calcium channels for depolarization; run transversely through muscle fibers  
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Sarcoplasmic Reticulum   Located on either side of the T-tubules; Stores (muscle relaxation), releases (muscle contraction), and sequesters calcium  
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Terminal cisterna   Site where T-tubule tells sarcoplasmic reticulum to release calcium for contraction; large sac-like structure  
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Triad   T-tubules, Terminal cisterna, and sarcoplasmic reticulum  
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Voluntary control   A neuron must tell the muscle what to do  
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Cardiac muscle   specialized striated muscle; involuntary  
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Development of cardiac muscle   Cardiomyocyte- located in walls of heart; generate electrical impulses of the heart; single or multi-nucleated  
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Contraction of cardiac muscle   Automaticity- spontaneous contraction Syncytium- single cell function and 1 (gap junction) because cells meet end to end; allows contractions to work together  
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Neural control of cardiac muscle   Autonomic nervous system- parasympathetic (relax) and sympathetic (stimulate) no neural muscular junction  
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Cardiac muscle functional structures   Sarcomere- T-tubules, SR, Mitochondria Intercolated disks with gap junctions  
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Sliding filament theory   during contraction the thin filaments slide past the thick filaments to they overlap; When sarcomere is contracted I-bands are gone and Z-discs are pulled to the center of the sarcomere  
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Cross-bridge cycling   4 steps; when actin bind to myosin we have a cross-bridge; Cycling- going back and forth between strong and weak bonds  
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Step 1 Cross-bridge cycling   Myosin binds to actin forming a cross-bridge  
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Step 2 Cross-bridge cycling   Phosphate falls off and myosin bends forward which draws thin filaments towards center of the sarcomere and ADP falls off  
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Step 3 Cross-bridge cycling   ATP binds to myosin and disassociates or weakens bond between actin and myosin  
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Step 4 Cross bridge cycling   Myosin will change ATP to ADP and phosphate and re-cocks the myosin head  
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Role of calcium in contraction   Calcium binds to troponin C; Troponin then triggers tropomyosin to move  
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Neuron muscular junction   Site where the neuron makes contact with the muscle  
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Buton (neurotransmitter)   Releases vessicles containing ACH (acetylcholine) into the synaptic cleft; ACH binds to receptors on Na and K channels; ACH opens channels in the cleft which causes membrane potential which initiates and raises membrane potential  
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After acetylcholine is used...   It is broken down and leaves the cleft  
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Action potential   When a membrane depolarizes and repolarizes; membrane can depolarize and recover in 4ms  
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Threshold   a point you must reach or exceed for something to occur; all or none; when threshold is met or exceeded sodium channels will open  
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Depolarization   Na channels will be signaled to open and sodium will rush in the cell; the membrane potential will become positive; this action moves down the sarcolema  
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Repolarization   When a section of the membrane has a positive potential the potassium channels will open allowing the membrane to be polarized again; this also moves down the sarcolema right behind the depolarization  
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After Depolarization/repolarization   The channels close and Na (out) and K (in) are pumped back to the appropriate sides of the membrane through sodium potassium pumps  
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Resting membrane potential   -90  
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depolarization and the triad   signal to depolarize can travel down T-tubules by the Na channels; this process signals sarcoplasmic reticulum through receptors; the SR then releases Ca to bind to troponin ect.  
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End plate potential   The rise in membrane potential of the cleft; gets to about -40 or -50 which meets threshold requirements and causes depolarization  
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When acetylcholine stops and membrane potential is positive...   channels open and membrane repolarizes  
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Twitch   muscle contraction stimulated by a single stimulus  
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3 periods of a twitch   1.Latent period 2.Contraction period 3. Relaxation period  
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Latent period   Beginning; everything up to myosin binding to actin  
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Contraction period   Middle; Myosin binds to actin; takes about 30ms to peak  
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Relaxation period   End; decreasing amount of tension  
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Slow vs fast twitch   twitch characteristics come from the metabolic properties of myofibrils; no difference in latent period  
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Fast twitch   Very quick to peak in the contraction period and very quick to fatigue  
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Slow twitch   Slower to peak in contraction period and slower to fatigue  
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Gastrocnemius   (fast twitch); quick to peak and quick to relax  
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Soleus   (slow twitch); longer to peak and longer to relax  
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Graded muscle responses (i.e. tension production)   1.Frequency stimulation 2.Amount of motor neurons activated  
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Frequency stimulation   crude; before the first contraction can relax we have a second contraction on top of the first; causes more force with the same muscle- energy is reserved and more Ca is being released to cause more reactions; can continue till max cross-bridges formed  
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motor neuron control   each fiber is controlled by a specific motor neuron but one motor neuron can be responsible for controlling 40-200 fibers  
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Amount of motor neurons activated   (size principle); as stimulus voltage increases the amount of fibers activated increases and higher the tension; high contraction force by increasing # of motor units contracting; smallest to largest  
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Smallest to largest   small units used for small tasks and vice versa; we can regulate force by regulating the motor neurons activated  
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Length tension relationship   optimal sarcomere length; too much contraction; too much stretching  
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Optimal sarcomere length   max number of cross bridges are formed  
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Over contracted   If we contract the sarcomere by too much the thin filaments will over lap and it will block binding sites so tension and # of cross-bridges will decrease; can continue to shorten until no more cross-bridges can be formed  
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Over stretched   If we extend the sarcomere by to much then tension and number of cross bridges will decrease as actin and myosin separate; will continue until no cross-bridges can be formed  
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Smooth muscle   Involuntary; not striated; single nucleated cells; found in the lining of most organs  
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Development in smooth muscle   Layers of cells can have different shapes- no cell phenotype; single, central nuclei;synchronous contractions due to cellular junctions; lacks organization; No sarcomere  
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Neural control in smooth muscle   Autonomic nervous system- parasympathetic, and sympathetic; no defined nerve ending plates  
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Contraction types of smooth muscle   1.Phasic contraction- single unit (gastrointestinal) 2.Tonic contraction- multiunit (blood vessels)  
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Layers of cells   longitudinal and circular layers of cells; they contract at different times; cells have gap junctions that tell the cells around them to contract  
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Autonomic nervous system   Norepineprine is released by a varicosity of an autonomic nerve fiber and can cause numerous muscles to contract (involuntary)  
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Varicosity   bulbous swelling of innervating nerves; release neurotransmitters into wide synaptic clefts called diffuse junctions  
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Intermediate filaments   cytoskeletal structure, helps give the cell characteristics like twisting while shortening  
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Caveolae   (poorly developed SR); receptor mediated, concentrates calcium, helps to take calcium from outside the cell to make up for poor SR  
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Thin to thick filament ratio (smooth muscle)   1 thick filament to every 13 thin filaments  
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Filaments in Smooth muscle   actin and myosin are not organized in sarcomeres; no troponin or tropomyosin  
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E-C coupling   Calcium is released into cell and binds to calmodulin; kinase phosphorilates myosin; the more phosphate groups the more contractions  
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Calmodulin   enzyme that phosphorilates kinase  
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Single unit contraction   single-unit muscle (visceral muscle); contracts rhythmically as a unit via gap junctions; may have spontaneous action potentials; arranged in opposing sheets to exhibit stress-relaxation response; (ex. gut contractions)  
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peristalsis   alternating contractions and relaxations of smooth muscle that mix and squeeze substances through the lumen (ex. stomach)  
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Mulit-unit   Rare gap junctions; infrequent spontaneous depolarizations; structurally independent muscle fibers; a rich nerve supply, may form motor units; graded contractions (ex. airways, blood vessels, arrector pili, internal eye)  
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Stress relaxation response   smooth muscle can expand due to a stimulus and if the expansion is held for long enough the muscle will then relax and allow more room for more tension all while keeping its ability to contract  
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hyperplasia   increase in the number of cells which may result in an increase of that organ; smooth muscles used this to undergo mitosis and increase number (only muscle that can divide)  
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Atherosclerosis   heart disease  
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Hyperplasia (estrogen and the uterus)   at puberty estrogen stimulates the synthesis of more smooth muscle which allows uterus to grow to adult size; also happens during pregnancy to accommodate the increasing size of the baby  
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