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movement, posture and position, stabilize, heat production
primary function of muscles
movement
responsible for locomotion(move the skeletal system), responsible for organ manipulation
posture and position
muscles function nearly continuously, small adjusting movements
stabilize
while moving joints, stabilization occurs to maintain bony articulation
heat production
generated with contration, plays a role in maintaining normal body temperature
skeletal, smooth, cardiac
muscle tissue types
myo, mys
muscle
sarco
flesh

epimysium, perimysium, fasicle, muscle fiber, endomysium, sarcolemma, myofibril
gross anatomy of skeletal muscles
myofibrils
rod-like contractile elements, “banded” appearance, made of sarcomeres
muscle fibers
elongated multinucleate cell, “banded” appearance, made of myofibrils, surrounded by endomysium(wrap sheath of areolar connective tissue)
fasicles
discrete bundle of muscle fibers, surrounded by perimysium(dense irregular connective tissue)
muscle
hundreds of thousands of fasicles, includes: blood vessels and nerves, surrounded by epimysium(dense irregular connective tissue)
direct and indirect
connecting to the skeleton
direct connection
“fleshy” attachment, epimysium is fused to the periosteum/pericondrium
indirect connection
tendon, apneurosis, can anchor to bone, cartilage and other muscles; more common
tendon
rope like anchor
aponeurosis
sheet anchor
sarcomere
contractile unit; composed of myofilaments made up of contractile proteins'; 1=z-disc to z-disc
myosin
splits ATP
titin
forms elastic filament
actin
binding site for myosin
tropomyosin
stabilize actin; block myosin binding sites(relaxed)
troponin
helps position tropomyosin and binds Ca+ ions
thick filament
many myosin molecules; around 300 heads

thin filament
two strands of actin twisted into a helix and 2 types of regulatory proteins

sarcomere zones
I band, H zone, M line, Outer edge of A band

I band
thin filaments only
H zone
thick filaments only
M line
thick filaments linked by accessory proteins
outer edge of A band
thick and thin band filaments
sarcoplasmic reticulum
elaborate smooth endoplasmic reticulum, loosley weaves around each myofibril(elongated sacs are terminated cisterns(always come in pairs), stores calcium
T tubules
formed by the sarcolemma, runs between terminal cisterns creating triads, allow for nerve stimulation to reach even the deepest sarcomeres
excitability, extensibility, elasticity, conductivity, contractility
universal characteristics of muscle
motor unit
one motor neuron and all the muscle fibers it innervates
motor neurons
aka somatic motor neurons and efferent somatic neurons, axon splits as it enters the muscle, split branches form the neuromuscular junction(motor end plate)
neuromuscular junction
only one per muscle fiber( around middle fiber), contain multiple axon terminals, very close to the muscle but technically separate(synaptic cleft)
muscle contration
motor neuron fires, release of ACh, ACh binds, depolarization; action potential triggered down the sarcolemma; AP travels to T tubules, release of Ca2+, Ca2+ binds to troponin; contraction
neuromuscular junction
synaptic vesicles(small membranous sacs), contains neurotransmitter acetylcholine(ACh), very close to the muscle but technically separate(synaptic cleft)
first step of neuromuscular junction
action potential arrives at axon terminal
second step of neuromuscular junction
voltage gated Ca2+ channels open. Ca2+ enters the axon terminal, moving fown the electrochemical gradient
third step of neuromuscular junction
Ca2+ entry causes ACh to be released
fourth step of neuromuscular junction
ACh diffuses across the synaptic cleft and binds to ACh receptors on the sarcolemma
fifth step of neuromuscular junction
ion channels now open to allow passage of Na+ into the muscle fiber and K+ out of the muscle fiber. (Na+>K+) results in depolarization(end plate potential)
sixth step of neuromuscular junction
Ach breaks down and is sweapt away from the junction(ion channels close)
action potential across the sarcolemma
once initiated, sweeps across entire sarcolemma; 3 phases: generation of end plate potential, 2. action potential depolarization, 3. repolarization
action potential
result of a predictable sequence of electrical changes
first step in excitation-contraction coupling
the action potential propagates along the sarcolemma and down the T tubules
second step in excitation-contraction coupling
as the ATP moves down the T-tubules, they change shape (voltage sensitive). change in shape leads to release of Ca2+ from the terminal cisterns, creating an increase of Ca2+ in the cytosol
third step in excitation-contraction coupling
Ca2+ binds to troponin causing it to change shape, and removes the blocking action of tropomyosin. results in the myosin binding sites of the actin to be exposed
fourth step in excitation-contraction coupling
contraction begins as the myosin heads are now able to form cross-bridges
sliding filament model of contraction
nervous system stimulates the muscle, 2. a cross bridge is formed, 3. thin filaments propelled towards center, 4. muscle cell shortens
cross bridge cycle
myosin head attaches to actin(cross bridge), 2. ADP and Pi are released(results in myosin head movement and flex of the cross bridge), 3. actin slides relative to myosin, 4. ATP attaches to myosin(releases from actin)
energy for muscle contraction
ATP
direct phosphorylation
no oxygen use; 1 ATP per CP, creatine made; 15 seconds of energy
anaerobic pathway
no oxygen use; 2 ATP per glucose and lactic acid made; 30-40 seconds of energy provided
aerobic pathway
oxygen use required; 32 ATP per glucose made, CO2, H2O; energy lasts hours
force
directly correlated to the number of myosin cross bridges that are attached to actin; four factors contribute to the strength of a muscle contraction(frequency, number, size, stretch)
velocity and duration
“how fast” and “how long”; three factors contribute to velocity and duration of muscle contraction(type, load, recruitment)
slow oxidative(type I) and fast glycolytic(type II)
subtypes of skeletal muscle
slow oxidative(type I)
endurance; smaller motor units; weaker motor unit strength; smaller relative diameter; aerobic ATP synthesis; good fatigue resistance; abundant and large mitochondria
fast glycolytic(type II)
quick/fast; larger motor unit size; stronger motor unit strength; larger diameter; anaerobic ATP synthesis; poor fatigue resistance; fewer and smaller mitchondria