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49 Cards in this Set

  • Front
  • Back
myosin stats
made of 200 - 500 myosin molecules
2 entwines polypeptides(look like golf clubs)
polypeptides
tails face the center and heads face the outside
central area of myosin
bare area with no heads, only tails
Actin
thin filament
two intertwines strans fibrous actin
globular actin with an active site
tropomyocin
long orange protein that stops mucles from contracting
Troponin
one small calcium binding molecule for each tropomyocin.
large amounts of calcium changes troponin shape, and pulls out topomyocin, causing a contraction.
contractile proteins
myosin and actin(doers)
Regulatory proteins
tropomyocin and troponin
steps of T & T
switch starts and stops muscle.
contraction activated by release of calcium into the sarcoplasm and its binding to troponin
troponin moves tropomyocin off the actin active site.
Dark Band
A band (thick filament region)
Myosin
Light Band
I Band (thin filament region)
Actin
gets shorter with contraction
sarcomere
from 1 Z-disk to the next is one sarcomere.
H zone
Light strand between dark bands.
Symatic motor neurons
make ACh- acetocoline
ATP Pump
makes a cell electrically excitable, by pumping Na, and K in and out of the cell.
Resting Membrane Potential
Inside the cell is -80/-90mV
Relax
Potasium is running inside the cell
Contract
Sodium going outside the cell
Electrical stimulus begins
when the pump runs
Muscle contraction and relaxation
1. excitation- nerve action potentials lead to action potentials in nerve fibers
2. Excitation contraction coupling- action potentials on the sarcolema activate myofilaments
3.Contraction- shorteing of muscle fiber
4. Relaxation- return to resting length
1. Excitation
Nerve signal opens voltage gated calcium stimulates exocytosis of synaptic vesicles containing ACh, then ACh releases into the Synaptic cleft.
Wave Peaks
when the wave peaks it will begative on the on the outside and positive on the inside.
membrane voltage
will determine whether the gate on the synaptic knob will open or close.
End Plate Petential
Binding ACh to Receptor Proteins will open Na and K channels resulting in a jump in RMP from -90 to + 75mV

Don't move anywhere.
Triggers action Plate.
Action Potential
Voltage change in EPP opens nearby voltage gated channels, this is like a wave

It does move.voltage gauged by sodium and potasium
2. Excitation Contraction Coupling
action potential spreading over sarcolema enters t-tubules voltage gated channels open in t-tubules causing calcium gates to open in SR
T-Tubules carry what?
action potentials through the sarcolema.
this electrical activity releases calcium from the sarcolema.
Calcium from SR
Binds to troponin, the toponin, tropomyocin complex changes shape and exposes active sites on actin.
3. Contraction
Myosin ATP in myosin head hydrolyzed on ATP molecule, activating the head and "cocking" it in on extended position
myosin head binds to actin active site forming cross bridge.
Power Stroke
myosin head releases ADP and phosphate as it flexes pulling the thin filament past the thick.
Sliding Filament Theory
thick and thin filaments dont become shorter, they just slide part eachother.
4.Relaxation
Nerve stimulus ceases ACh- sterase removes ACH from receptors, stimulation of the muscle cell ceases.
In relations Active Transport
Pumps calcium back into the SR, through active calcium pumps.
relaxation and ATp
ATP is needed for relaxation as well as contraction.
Rigamortis
calcium leaks from SR, causing the muscles to contract.
Exocytosis
is triggered by calcium
Calcium Channels
open during voltage change and calcium then difuses in SR and bonds with troponin
AChe
is found in Synaptic CLeft, eats away ACH when not absorbed.
Length Tension Relationship
Amount of tension generated depends on length of muscle, or sarcomere before it was stimulated.
Overly COntracted
Weak!
Thick filament to close to Z disk and cant slide.
too Stretched
Weak!
little overlap of thin and thick does not allow for ery many cross bridges to form.
Optimum Resting Length
Produces greatest Force.
Threshold
voltage producing on action potential.
Twitch
a single breif stimulus at that voltage produces a quick cycle of contraction and relaxation, lasting less than 1/10 of a second.
single twitch is very weak.
Latent Period
the time between the stimulus starts and when the contraction begins.
Threshold Stimuli
Produces twitches, but twitches of individual muscle fibers remain unchanged despite increased voltage.
variability in contraction
due to Ca2 concentration, previus stretch of the muscle, temperture, ph, and hydration.
Recruitment and stimulus intensity
stimulating a whole nerve with higher voltage produces stronger contractions
Multiple Motor Unit Summation
More motor units are being recruited
also known as spatial summation