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Smooth muscle
- Internal organs, blood vessels, eye. Produce movements in internal organs.
- involuntary, single nuclei, non-striated, spindle-shaped
- nerve supply to visceral modifies, nerve supply to MULTIUNIT is necessary
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Cardiac muscle
- Heart. Pumps blood.
- Single nuclei, striated, branched, involuntary
- nerve supply not necessary for function--modifies
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Skeletal muscle
- skeletal muscles. Moves bones, generates heat.
- Voluntary. Multi-nuclei, striated, long, thin fibers.
- Nerve supply necessary for movement
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epimysium
connective tissue that encircles all fascicles to form a complete muscle
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perimysium
connective tissue that encircles a group of muscle fibers forming a fascicle
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Fascicle
a group of muscle fibers (held together by a perimysium)
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Endomysium
connective tissue that surrounds each muscle fiber or cell.
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Tendon
where epimysium, perimysium and endomysium come together to attach to a bone
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Sarcoplasm
muscle cytoplasm
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sarcoplasmic reticulum
- muscle endoplasmic reticulum
- surrounds each myofibril. Inside, lots of CALCIUM
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Sarcolemma
plasma membrane of a muscle cell
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T(ransverse)-tubules
- invaginations of the sarcolemma into the inside of the muscle at a right angle.
- Action potential travels inside of them to stimulate SR and release calcium for contraction
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Actin
- thin filament in muscles. In I-band (across Z-line) in a sarcomere. Double helix made of F-actin (string) and G-actin molecules (pearls).
- Tropomyosin and troponin attached. Moved by myosin
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Myosin
- thick filament. Tail, hinge and head. Head has ATP/ADP and phosphate to help move actin filament.
- Makes up H-zone in sarcomere.
- All heads in the same direction (on each side). Tails point towards the H-zone
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Organization of skeletal muscles
- Muscle bundle
- muscle fiber
- myofibril
- sarcomere
- (myofilaments) actin and myosin filaments
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Z-line
boundaries of a single sarcomere. Includes actin and myosin filaments (half I-band, A-band, H-zone)
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A-band
section of a sarcomere containing myosin. Some actin is inside too
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I-band
section in sarcomere that contains only actin, spans the Z-line so half is in each sarcomere. Disappears as muscle contracts
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H-zone
portion of sarcomere that contains only myosin, in the middle. Disappears as muscle contracts.
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F actin
string part of double helix that makes up actin filament
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G-actin
pearls of actin filament
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Triad
A T-tubule and two terminal cisternaes (part of sarcoplasmic reticulum)
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Dihydropyradine receptor
DHP, on T-tubule. Receptor that depolarizes to signal the Ryanodine (RyR) receptor and allow calcium out of the sarcoplasmic reticulum
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Ryanodine receptor
on sarcoplasmic reticulum, receptor that opens when DHP is depolarized to release calcium into the cell and cause muscle contraction
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Tropomyosin
evil stepmother that covers myosin binding sites on the actin filament until distracted by a calcium-troponin bond.
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Troponin
Tiny bubbles on tropomyosin with three sub-units (bond to G-actin, Calcium or Tropomyosin)
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Power stroke
when myosin filaments move actin filaments toward the H-zone, contracting the muscle.
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Actin and myosin contraction
action potential goes through DHP, RyR releases calcium, calcium binds to Troponin, Troponin-Ca moves Tropomyosin, Myosin binds to Actin, Myosin hinges move actin towards the H-zone (due to release of ADP and P), causing the power-stroke that contracts the muscle, ATP phosphorylates, re-cocking the hinge
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Termination of muscle contraction
energy (ATP) is required to pump Ca2+ back into sarcoplasmic reticulum. Everything releases back into its original form.
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Action potential from cardiac muscle is different because:
it contains a plateau instead of a spike, caused by opening of voltage-gated calcium channels (slower). Slower depolarization, extends before repolarization. Longer absolute refractory period creates a forced pause between beats for the ventricles to fill (no tetany)
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Strength of muscle tension is dependant on
length of sarcomere pre-contraction. Maximum number of cross bridges is ideal--should be overlap but still contain an h-zone and I-zones.
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Twitch (3, last one has 3)
- single instant reaction of muscle, 20-200 milliseconds, goes through phases one time.
- Neuro action potential (spike)
- Muscle action potential (wider, a little less spike)
- Muscle contraction (Latent, contraction, relaxation)
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phases of muscle contraction
- latent (action potential to calcium release)
- contraction (calcium release to power stroke)
- Relaxation (calcium pumped back into SR, ADP/ATP released to recock myosin head)
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Treppe
A gain of muscle twitch (more forceful but not longer) caused by a second stimulation shortly AFTER the relaxation phase of the first twitch. Not all calcium was pumped back into SR so there is more force/tension.
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wave summation
- gain of muscle reaction (stronger AND longer) caused by second stimulation DURING relaxation phase. Makes for a graded or sustained contraction, smoother response.
- Can result in FUSED tetanus, for smooth contraction
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Fused tetanus
during wave summation when so many impulses are coming so fast that reactions become constant and smooth. A contraction. Graded, smooth, continuous.
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Tetanus
stimuli coming quickly, twitch goes through fused summation for a prolonged contraction. (Normal)
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Spatial Summation
- Greater force of muscle contraction by INCREASING the number of motor units that fire at one time. (more motor units will cause a contraction to get stronger/longer)
- AKA multiple motor unit summation or recruitment summation
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Multiple motor unit summation
Greater force of muscle contraction by INCREASING the number of motor units that fire at one time. (more motor units will cause a contraction to get stronger/longer)AKA spatial summation or recruitment summation
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recruitment summation
Greater force of muscle contraction by INCREASING the number of motor units that fire at one time. (more motor units will cause a contraction to get stronger/longer)AKA multiple motor unit summation or spatial summation
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Delicacy of muscle motion
- is dependant on number of fibers controlled by a single motor unit--less is more.
- Smaller motor muscle unit=more delicate movement
- larger muscle motor unit=less precise movement
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phosphocreatine
- storage for ATP in muscle. Short-term, so more needs to be made constantly. Stored during rest.
- phosphocreatine + ADP --(creatine kinase)--> creatine + ATP
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Ways for muscle to get ATP
- creatine-phosphate (into creatine, into ATP)
- Anaerobic (glycogen by glycolosis into lactic acid into ATP)
- Aerobic (Most, cellular respiration, electron transport chain)
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How can you interefere with muscle synapse?
- Block release of ACH
- too much ACH
- No breakdown of ACH
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What was wrong with Maggie? Wound, flaccid paralysis, weak tongue, eyelid tone, difficulty chewing and swallowing.
Botulism. Food poisoning, wound poisoning in horses. Toxin interrupts nerve transmission--prevents release of ACH. Acute symptoms. treated with antitoxin and antibiotics.
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What was wrong with Fifi? Fatigue and exercise-induced weakness, change in voice, vomiting.
Myasthenia Gravis. antibodies attacking nicotinic receptors, blocking action potential. Can cause megaesophagus. Often in dogs, rarely in cats. Give tensulin--quick easy test that exposes nicotinic sites and temporarily cures symptoms
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