ability to respond to stimuli by changing membrane potential
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Condutivity
sending and electrical charge down the length of the plasma membrane
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Contractiility
proteins slide against one another-
muscle cells cause body movement
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Extensibility
ability to be stretched and lengthened
proteins slide and reduce overlap
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Elasticity
ability of cell to return to original length after shortened or lengthened
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what is elasticity dependent upon?
extensibility and contractiility
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why is skeletal muscle considered an organ?
many tissue types
CT, bv, nerves, muscle fibers
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fasicle
bundle of muscle fibers
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how many fascicles in muscle?
many
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muscle fibers
muscle cells
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Layers of skeletal muscle
epimysium perimysium endomysium
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epimysium
surrounds entire muscle
DENSE IRREG
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perimysium
surrounds fascicles bv and nerves
DENSE IRREG
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Endomysium
surrounds each muscle fiber insulation, support, binds neighboring cells
AREOLAR
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tendon
Connects muscle to bone
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common properties of tendons and aponeurosis
attachments of muscle to muscle, skin, bone
made from fibers of epi, peri, endo collective fibers
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what type of tissue is in tendons?
dense regular
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Aponeurosis
strong sheet of tissue that acts as a tendon to attach muscles to bone
btw frontal and occipital head
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what type of tissue is in aponeurosis?
dense irregular
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deep fascia
superficial to epimyisum
separates individual muscles, binds muscles with similar functions
bv, nerves, lymph
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what type of tissue is deep fasica made of?
dense irregular
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superficial fascia
separates muscle from skin
superficial to deep fascia
BARRIER
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what type of tissue is superficial fascia made of?
areolar/adipose
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blood vessel/nerve properties of skeletal muscle
vasculairzed-removes wastes, delivers oxygen
innervated by somatic neurons-voluntarily control of muscle
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sacroplasm
cytoplasm of a muscle cell
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what does the sarcoplasm contain?
organelles and cytosol
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how are muscle cells multinucleated?
myoblasts fuse together
some become satellite cells-support/repair
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sacrolemma
plasma membrane of a muscle cell
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T-tubules (transverse tubules)
deep invaginations of the plasma membrane
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channels in T-tuble and sacrolemma
VGC allow for electrical signals
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voltage sensitive calcium channels
responsive to the electrical signals (action potentials)
IN SARCOLEMMA
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myofibrils
bundles of myofilaments enclosed in sarcoplasmic reticulum
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How many myofibrils are in each muscle fiber?
100s-1000s
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sacroplasmic reticulum
internal membrane complex similar to smooth ER
contains Ca pumps/calcium release channels
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terminal cisternae
blind sacs of sarcoplasmic reticulum serve as reservoirs for Ca ions
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triad
two terminal cisternae and a T tubule
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calcium release channels
Triggered by electrical signal traveling down T-tubule
calcium released into sarcoplasm
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myofilaments
contractile proteins
thick/thin
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thick filaments
myosin
heads point towards end of filament
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thin filaments
actin, troponin, tropomyosin
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troponin
globular protein, Ca binding site, pulls tropomyosin off
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tropomyosin
covers myosin binding sites on the actin molecules
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f actin
G actins polymerized into a double helix
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g actin
myosin binding site
monomer of f actin
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sacromeres
myofilaments are organized into repeating functional units
thick/thin filaments
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z lines
The ends of the sacromeres that cause contractions of a muscle
ANCHOR FOR THIN FILAMENTS
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I bands
light bands
thin filaments b
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what are the I bands bisected by?
Z discs
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A band
dark area
thick filaments, some thin contains H zone and M line
CENTER OF SACROMERE
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H zone
Central region of A-band thick filaments
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M line
middle of H band
attachment site for thick filaments
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What anchors the thin filaments?
Z disc
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What anchors thick filaments together?
M line
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connectin
Extends from Z disc to M line
Stabilizes thick filaments
"springlike" properties (passive tension)
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dystrophin
Anchors some myofibrils to sarcolemma proteins Abnormalities of this protein cause muscular dystrophy
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Duchenne Muscular Dystrophy (DMD)
defective/insufficient dystrophin
sarcolemma damaged during contraction -ca enters cell, damage
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what age do most patients with DMD survive to?
30
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myoglobin
stores oxygen in muscle cells for ATP production
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where is glucose stored
liver and skeletal muscle
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creatine phosphate
phosphate from creatine phosphate can be removed and attached to an ADP to generate ATP quickly.
10-15 sec of energy
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catalyst in creatine phosphate
creatine kinase
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motor unit
A motor neuron and all of the muscle fibers it innervates
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small motor units
less than five muscle fibers -allow for precise control of force output
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large motor units
thousands of muscle fibers -allow for production of large amount of force but not precise control
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location of fibers of motor unit
dispersed throughout muscle
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synaptic knob
rounded areas on the end of the axon terminals
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synaptic vesicles
saclike structures found inside the synaptic knob containing AcH
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channels in synaptic knob
ca pumps, VGC Ca
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motor end plate
specialized part of a muscle fiber membrane at a neuromuscular junction
many AcH receptors
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synaptic cleft
separates knob from motor end plate
Acetylorichase resides here
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actetylcholinesterase
an enzyme that breaks down acetylcholine
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neuromuscular junction
Location where motor neuron innervates muscle
Has synaptic knob, synaptic cleft, motor end plate
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resting membrane potential skeletal muscle
-90mV
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Calcium entry at synaptic knob
•Nerve signal travels down axon, opens voltage-gated Ca2+ channels •Ca2+ diffuses into synaptic knob •Ca2+ binds to proteins on surface of synaptic vesicles
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Release of ACh from synaptic knob
-vesicles merge with cell membrane at synaptic knob: exocytosis -thousands of ACh molecules released from about 300 vesicles
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excitation-contraction coupling
sequence of events from motor neuron signaling to a skeletal muscle fiber to contraction of the fiber's sarcomeres
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end plate potential (EPP)
ach receptors open when Ach binds to them
Na diffuses into cell, little K out
EPP is local but is graded potential
opens VGC
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How does EPP reach threshold?
by causing nearby voltage-gated Na+ channels to open
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depolarization of skeletal muscle
30 mV
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the release of Ca from the sarcoplasmic reticulum
Ca interacts with myofilaments triggering contraction
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crossbridge cycle
crossbridge formation: binding of myosin to myosin binding site and actin to actin binding site
power stroke: myosin pulls on actin, ADP and Pi released
release of myosin head: ATP binds to myosin head causing its release from actin
reset myosin head: ATP split ADP and Pi, cocks myosin head
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what is needed for crossbridge cycling?
Ca and ATP
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steps of cross bridge cycle
cross bridge formation
power stroke
cross bridge detachment
cocking of myosin head
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cross bridge formation
myosin heads attach to the active site on actin
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power stroke
action of myosin pulling actin inward (toward the M line)
ADP and P1 released
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what happens when ADP is released in crossbridge?
moves actin to m line
POWERSTROKE
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what happens when phosphate is released in crossbridge?
bonds get stronger
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cross bridge detachment
ATP attaches to myosin head, causing cross bridge to detach
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cocking of myosin head
As ATP is hydrolyzed to ADP and Pi, the myosin head returns to its prestroke high-energy, or "cocked" position
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hydrolize
break down (a compound) by chemical reaction with water.
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muscle relaxation
AP ends, electrical stimulation of SR stops
Ca2+ pumped back into SR Stored until next AP arrives Requires ATP
Without Ca2+, troponin and tropomyosin return to resting conformation Covers myosin-binding site Prevents actin-myosin cross-bridging
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storage of ATP in muscle cells
little
spent after 5 seconds of exertion
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myokinase
transfers Pi from one ADP to another, converting the latter to ATP
makes additional ATP rapidly
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Ways to generate ATP in skeletal muscle fiber
-Immediate supply via phosphate transfer -Short-term supply via glycolysis -Long-term supply via aerobic cellular respiration