Escolar Documentos
Profissional Documentos
Cultura Documentos
Dana Little
Section: 8
The muscular system is important for normal body functioning. There three
types of muscles, cardiac muscle are found in the heart to pump blood throughout
the body. Smooth muscles control the contractions of organs. Skeletal muscles
have two functions, to generate and shorten force, and contract to the response of
electrical and chemical signals. Skeletal muscles consist of muscle fibers made of
myofibrils for contracting. Myofibrils are made of actin filaments and thick myosin
filaments which when they over lap makes the muscle contract. The length of the
Signals from the brain sends signals to the spinal cord, where moto neurons
stimulate the muscle fibers. The motor unit consist of motor neurons and the
muscle fibers. The human body has many muscle units large and small which
depends the movement. Large muscle fibers produce large forces, small motor
units have fewer muscles for finer movements. Smaller motors are stimulated first
and then larger ones to conserve energy. However artificial stimulation can
potential which travels to the nerve cell and to the muscle fibers. When a
stimulated the never cells release calcium ion to trigger acetylcholine to release.
then also open and repolarizes the cell, which creates and second action potential.
and the interaction of actin and myosin cross bridges. The muscle is now relaxed
and is ready for another contraction. A twitch is a small muscle contraction cause
and frequency of stimulation allows for more motor units for recruitment resulting
the muscle fiber causes a second stimulation before it can relax. If the voltage is
high enough the fibers will be stimulated rapidly so there is no time for relaxation
The purpose of this lab is to understand skeletal muscle contraction and how
force is affected manipulating different factors. The stimulator sends pulses though
the sciatic nerve and the gastrocnemius muscle on the frog. By changing the
intensity and frequency of the stimulus and recording the forces produced and
observe the differences in the twitches. We also observe the effects of tunocurare
of the gastrocnemius frog muscle. At the end we saw that increasing the stimulus
resulted in an increase in the force until it has reached its maximum. When we
increased the frequency is caused an increase in a force until the muscle has
reached tetanus. When we injected the tubocurarine it inhibited muscle contraction,
by using electrodes we can directly stimulate the muscle with the capabilities of by
Methods:
then sperate the skin and carefully isolating the gastrocnemius from the tendon by Commented [DCL1]:
cutting away the bone at the heel. We then tie a 9-inch string to the gastrocnemius.
To keep the frog moist, we periodically applied Ringers saline solution to the frog.
Next, we exposed the sciatic nerve between the quadriceps and hamstring muscles.
The sciatic nerve was a thin white line extending from the knee to the hips. By
using a glass probe, we were able to free the nerve and place a 4 inch sting under
it. We then placed a parafilm to separate the nerve from the muscle to prevent the
electrode from stimulating the muscles at the wrong place. The artificial stimulator
sends electrical pules to the frog and the BioPac program places the response on to
a graph. First, we much calibrate the transducer by hanging a 20g weight with an S
hook. We then clamp the frog’s gastrocnemius junction to hold the leg in place.
The 9 inch string is now hung to the transducer at a 90 degree from the lower leg.
Double checking all our leads and dials are at the correct settings and hung the
maximum voltage threshold. The stimulator settings set to the Table found on page
13, the stimulator slowly increases until a twitch occurs which a peak on the
BioPac. The threshold is the lowest voltage needed to make a twitch. Switching it
to single and slowly increase the voltage until peaks no longer increases meaning
we have reached out maximum. Voltage maximum is the lowest voltage needed to
We found our voltage threshold and maximum. Before starting our second
experiment, we must check our tension again and adjust it back to between 20-30
frequency at 0.5 pps and switch it to repeat for 15 seconds. We then tested
frequency at 1.0, 2.0, 4.0,8.0, 15, and 25pps. We waited 30 seconds in-between test
In the third experiment we observed how inhiation will lower the number of
the acetylcholine receptors that are able to bind to acetylcholine and produce a
twitch. We often had to reassure that our leg tension 20-30 grams. Before injecting
tubocurare by our TA, we switch the stimulator to repeat and recorded for 1 minute
to observe the stimulation without the inhibitor. Next our TA injected .25ml of
indirectly stimulating. Two metal electrodes are inserted about 5mm apart in the
leg and connected to the stimulator. The begin the situation by increasing the
voltage until we see a response which our voltage threshold for the direct
stimulation will be. We recorded for 30 seconds and increased the voltage until the
peaks no longer increased which will be our voltage max for direct stimulation.
Results
Setting
V Threshold 0.22
V Max 0.375
Change in V 0.02