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skeletal muscle is under (voluntary/involuntary) control
voluntary
what causes skeletal muscle striation?
organized arrangement of actin and myosin (striations when viewed under microscope)
point of muscle attachment closest to the spine (proximal)
origin
point of muscle attachment on the far side of the joint (distal)
insertion
tendons
connective tissue at the end of muscle where points of attachment occur
what two muscles are on either side of a joint?
flexors and extensors
muscle fibers
skeletal muscle cells
endomysium
connective tissue layer surrounding muscle fibers
fascicles
grouped muscle fibers
perimysium
connective tissue layer surrounding fascicles, contains blood vessels and nerves
epimysium
connective tissue surrounding muscle
muscle
bundle of fascicles
tendon
grouping of connective tissue layers, joins muscle to skeleton
myotendinous junction
region of tendon where muscle fiber ends transmit force of contraction to tendon to effect skeletal movement
what are muscle connective tissues made of
elastin and collagen
myofibril
filaments running along axis of skeletal muscle cells
Z lines
two dark bands marking end of sarcomere (2 um)
I band
light bands on either side of Z line, contains thin actin filaments
A band
area between two I bands, contains thick myosin filaments
H band
light area in center of sarcomere, where no thick-thin overlap is
M line
center of sarcomere, contains proteins critical for organization and alignment
T tubules
invaginations of sarcolemma passing into fibers near A bands
(T tubules / SR) are in contact with extracellular space
T tubules
terminal cisternae
portion of SR nearest T tubules, site of Ca release
SERCA
Ca pump reuptake protein
thin filament structure
two stranded helical F-actin made of G-actin molecule aggregates, length regulated by cytoskeletal protein nebulin
tropomyosin structure and function
cover myosin-binding sites, dimers consisting of T, I, C subunit complex
tropomodulin function and location
end of thin filament, sets length
what proteins anchor thin filament to Z line?
CapZ and a-actinin
what protein contribute to thick filament structure?
titin, myomesin, and C protein
in what directions is contraction force transmitted?
longitudinally via tendon (myotendinous junction)
laterally to adjacent extracellular connective tissue (costameres)
costameres
sub-membranous, Z-line associated structures that transmit force and stabolize sarcolemma
dystrophin function and associated disease
maintains sarcolemma structure via dystrophin-glycoprotein complex connection to ECM
X-linked recessive deficiency results in Duchenne’s muscular dystrophy
what are some types of muscle dystrophy and their associated defects?
limb-girdle muscular dystrophy 2B - defect in sarcolemma repair and dysferlin
limb-girdle muscular dystrophy 2 and tibial muscular dystrophy - defects in titin
limb-girdle muscular dystrophy 2A - defects in calpain 3 protease
thick filament structure organized by heavy and light chains
2 heavy chains - backbone and N-term globular head
4 light chains - connecting heavy chain regions
essential vs regulatory light chains in myosin
essential - crucial for ATPase activity
regulatory - influences myson-actin interaction when phosphorylated
a motor neuron
innervates skeletal muscle
how does brain input get to muscles?
transmission to a motor neuronal cell body in ventral horn, transmission through ventral root
motor unit
motor nerve and all muscle fibers in innervates, functional contractile unit
how is fine motor control initiated?
activation of motor units with a small number of fibers
end plate
neuromuscular junction formed by motor neuron
tetany
increasing tension by repetitive stimulation of the muscle