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Muscle cell properties
contractibility
Excitability(response to chemicals and hormones)
Conductivity(cells travel through electricity)
Distensiblity(elongation without damage)
Elasticity(returned to normal state)
Neuromuscular Junction
synapse where a single motor neuron communicate
Transmit signals from neuron to sacrolemma of muscles fiber
Three components: axon terminal, synaptic cleft, motor end plate
Excitation phase
action potential arrives at axon terminal, triggers, calcium channel to open
Calcium ions, move into the action terminal and trigger exocytosis synaptic vesicles
Synaptic vesicles release ACH into synaptic cleft
ACH binds to receptors on motor end plate
Sodium ion channels open and sodium enters muscle fiber
Sodium entry, depolarizes, sarcolemma, creating, and plate potential
VIDEO:https://mediaplayer.pearsoncmg.com/assets/_z_QVtvni1EUXVBVXaeWRbRFdEs7sV_g
Excitation Contraction Coupling
and complete potential stimulates on action potential
Action potential is propagated down the T-Tubles
T-Tuble depolarize leads to opening of calcium ion channel is SR and calcium ions enter cytosol
Calcium ions bond to tropnin
Tropomysin moose and active sites on Actin are exposed
VIDEO:https://mediaplayer.pearsoncmg.com/assets/apf-excitation-contraction-coupling
Contraction-cross bridge
ATP Hydrolysis “cock” the myosin head
Myosin head binds to Actin
Powerstroke occurs when phosphate, detached, myosin head and myosin pulls Actin towards the center of the sarcolemma
ATP breaks the attachment of myosin to Actin
VIDEO:https://mediaplayer.pearsoncmg.com/assets/5QBacoiPZ_QDy46rzobIBu9WIiGf125a
Muscle relaxation
Actylcholinsterase degrades remaining ACH and re-polarize occurs
Circle lemma returns, resting, and calcium ion channels in the SR close
Calcium is pumped back into the SR
Troponin shifts and pulls trypomyosin back into position to block active sites of Actin and muscle relaxes
VIDEO:https://mediaplayer.pearsoncmg.com/assets/FBw0ZSz7qfmIzeSTm3Fxh8Lo0zO8OoEg
A tendon-place where epimysium blends into a rope-like connection that links muscle to bone
B epimysium-connective tissue "overcoat" covering entire muscle
D muscle fiber-make up the fascicles; also known as a muscle cell allows contractibility
E endomysium- connective tissue layer that covers each individual muscle fiber surrounded by the ECM
F muscle fasciculi-visible bundles composed of muscle fibers that make up the whole muscle
G perimysium-connective tissue that covers muscle fasciculi (fascicle)
H Bone
Osteon
dense part of bone circular
Central canal
blood vessels, parallel to the osteon lined with connective tissue called endosteum(inner layer of osteoblast, which secrete bone ECM and osteoclast)
Perforating canal
perpendicular to Lamelle carry blood vessels deep into Periosteum
Lamellae
lines bone ECM give strength
Lacunae
pockets, and layer of matrix osteocytes live in it
Osteocyte
mature bone cells
Canaliculi
Tiny passage ways, allowed diffusion in nutrients and waste
Periosteum
membrane, blood vessels, nerves, attach, dense, irregular, connective tissue outside a bone
Endosteum
inside lining bone marrow covers trabeculae
Sarcolemma
muscle fibers plasma membrane
T Tubule
stores, calcium ions
Modified smooth, endoplastic reticulum
Sarcoplasmic reticulum
Myofibril are wrapped in
Terminal Cisternae
on either side of the T-tubule
Triad
1 T-Tubule
2 terminal cisternae
Myofibril
small cyndricil organelles
Myofilment
protein subunits
Thick fillment
Composed of myosin
Contractive protein
Thin filament
composed of Actin
Contractile protein
A band
dense region of striations
Overlap, thick and thin fill or only thick
I band
lighter region
Only thin
Z disc
middle of I band
Structural protein
H zone
middle of a band
Thick
M line
runs down H zone
Structural protein
Sliding fillment theory
filament move inward(towards M line) which make the Z disc closer
Resting potential
voltage in cell negative compared to outside
Solute move by
leak channel-always open to allow ion move( passive transport hide to low)
Gated-closed at rest, certain ions stimulated to open
Electrochemical gradient
Concentration ions, diffuse hide to low
Electrical-look at charge and goes to the opposite, like charges repel
This builds to the electro chemical gradient which has sodium move and cell due to it being positive and wants to move towards the negative part of the cell, and then the potassium moves on a concentration gradient
Action potential
Quick temporary change move negative inside to positive
Resting stage-muscle at -90 mill volts during rest
Depolarization-sodium moves in more positive in cell
Re-polarization-sodium potassium get pushed outside the cell inside us now negative
Propagation-continuation of this is a wave all throughout the cell
The three stages of electricity in excitability in a cell
resting potential
Solute move
Action potential
Anaerbobic Catabolism
Glycolysis
Glucose sources-food blood to muscle FORM 2 ATP
Anaerobic-no oxygen
Fate of Pyruvate- pyruvate turns into lactic acid
Creatine phosphate
has ATP extra phosphate, quick energy
Aerobic Catabolism
oxidative-reduction reaction
Fuel source glucose
Aerobic-oxygen
Myoglobin-help blood hold onto oxygen
Gain 30 ATP in crab cycle
Long lasting
Muscle twitches three phases
Latent Period-time for action potential to propagate into sarcolemma
Contraction-repeated Crossbridge cycles generate tension
Relaxation-calcium ions are reduced in inside of cell by SR pumps
* Refractory Period-between the start of Latent . And into the contraction. Where muscle fibers can't respond to another stimulus.
Wave summation
waves of messages together create one whole message
Unfused Tetanus
tension gets stronger
Fused Tetanus
Complete contraction, muscle no time to act, tension constant
Length-tension relationship
shorted muscle hit limit
Overstretch hit limit
Type one skeletal fibers-dark muscle
Small, slow, not a lot of tension
“never wear out”
Oxidative mitochondria
Slow twitch
Oxidative fiber
Type two skeletal fiber-light muscle
contract quickly
Fast and powerful
Fatigue easy
Glycolysis
Fast twitch and glycolic fibers
Motor units
larger means more fibers to respond
Fine VS gross control
Fine control-precise control small motor unit
Gross control-large units, powerful contractions
Recruitment
initiation of contraction
Muscle tone
when at rest muscle stay somewhat contracted
Hypotonia VS hypertonia
hypotonia-low muscle tone due to injury
Hypertonia-high muscle tone due to things like working out
Isotonic contraction
cause muscle to change and length
Concentric VS Eccentric
concentric-muscle tension exceeds resistance
Eccentric-elongated muscle decrease intention
Isometric
muscle contraction cannot overcome tension
Endurance training
repetitious less weight increase contracting muscles
Need energy increase the number of mitochondria
Need oxygen
Resistance
weight fewer repetitions
Muscles hypertrofify(increase in size) decrease in mitochondria
Disuse
muscles don't get used less toned atrophy
Muscle fatigue
inability to maintain a level of intensity
Depletion in metabolic and oxygen
Recovery Period
breathe fast, which increases oxygen which increases lactic acid