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Structure and Function of Muscle
SKELETAL SMOOTH CARDIAC
METHOD OF CONTROL VOLUNTARY INVOLUNTARY INVOLUNTARY
BANDING PATTERN STRIATED NON-STRIATED STRIATED
NUCLEI/CELL MULTI SINGLE SINGLE
Muscle Types
Cardiac Muscle
Smooth Muscle
Skeletal Muscle
Muscle Cross Sections Showing Bundles of
Myofibers
FAT CELL
BLOOD VESSEL
Cross Section of Muscle Fibers
NUCLEI
Myofiber
Red and White Fibers in Muscle
Fiber types
The Blood Supply for Myofibers
Connective Tissues
Position of Mysiums in Muscle
ENDO = within
PERI = around
EPI = upon
Endomysium
Perimysium
Epimysium
• Endomysium from
muscle not aged
• Endomysium after
cooler aging (28 D
At 4oC)
The Sarcoplasmic Reticulum
• Sarcoplasmic reticulum
– T-tubule
• Calcium Storage
• Required for contraction
Structure of Muscle
Structure of Muscle (Cont)
Sarcomere
• Functional unit of a muscle
• Runs from z-line to z-line
– Actin
– Myosin
Myosin Filament
Actin Filament
Muscle Structure
Critical Contractile Proteins
REVIEW
Fat Structures
A
D
I
P
O
S
E
T
I
S
S
U
E
BLOOD VESSEL
ADIPOCYTE
ADIPOCYTES
Fat Layers and Depots
I.F. = Inter-fasicular or
intramucular (marbling)
I.M. = Intermuscular
(seam fat)
PR. = Perinephric or Peri-
renal (fat around the
kidneys)
FAT CELLS
Adipoblasts develop at widely varying
rates in different parts of the body.
Adipogenesis
• Adipoblasts
– 20 microns in diameter
• Adipocytes
– 120 micron in diameter
– 300 micron in obese
• Cellular make-up
– 95% of cytoplasm is lipid
– Remainder primarily nucleus
A
D
I
P
O
C
Y
T
E
HOW ARE
ADIPOCYTES
FORMED?
ONCE RECRUITED & FILLED, AN
ADIPOCYTE IS EASIER TO FILL AGAIN
THAN IF NOT FILLED BEFORE
Adipose cells
begin to
accumulate
When filled with lipid, it is a
mature adipocyte
Muscle Contraction
Introduction
• Overall structure of muscle is designed for
contraction and relaxation, which leads to
movement and locomotion.
• The ability to contract and relax is lost during
the transformation of muscle to meat.
• Events surrounding this conversion greatly
impact meat palatability
Introduction
• The biochemical processes that provide energy
to the living muscle cause the accumulation of
metabolites during harvest
– Affects color, WHC, pH, others
• An understanding of muscle contraction is
necessary to understand these processes
Contraction
• Begins with stimuli that arrive at the surface of
the muscle fiber at the sarcolemma
• Nerve impulse starts in the brain and is
transmitted via nerves to the muscle
Transmembrane Potentials
• Under resting conditions, an electric potential
exists between the inside and outside of the
cell
– Fluids inside are negative
– Fluids outside are positive
– Results in a resting membrane potential
Transmembrane Potentials
• Extracellular – Na+ and Cl-
• Intracellular – K+ and A-
• Na+ and K+ gradient maintained by a sodium-
potassium pump.
Action Potential
• Transmits electric impulse to muscle
• Travels along the membrane surface of the nerve
fiber by depolarization
– Initiated by a dramatic increase in the permeability of
Na+
– Na+ rushes into cell to establish equilibrium; however
K+ stays in cell causing a change in the net charge
inside the cell to positive
• Lasts only a millisecond (0.5 to 1 millisecond) before the
permeability to Na+ is changed to resting state
Myoneural Junction
• Action potential is not strong enough to elicit a
response alone
• Uses a chemical transmitter called
acetylcholine to be released.
– Acetylcholinesterase is quickly released to
neutralize the acetylcholine
Muscle Action Potentials
• Same as the action potential for nerve fibers
• Communicated to the inner muscle cell via the
T-tubule system
– Action potential transverse a muscle fiber via the t-
tubules and are ultimately responsible for the
release of calcium from the SR
Sarcomere - Basic contractile unit of the muscle
1. Myosin
2. Actin
a) Tropomyosin
b) Troponin
3. Z lines
Elements required for muscle contraction and
relaxation
1. Acetylcholine and Acetylcholinesterase
2. Calcium
3. Adenosine 5'-triphosphate (ATP)
a) Derived from aerobic and anaerobic
metabolism
Sources of Energy for Muscle
Contraction and Relaxation
Energy
• Aerobic
– Glycolysis
– TCA cycle
– Electron transport chain
• Anerobic
– Excess Hydrogen is used to reduce pyruvic
acid to lactic acid, which permits glycolysis to
proceed at a rapid rate
– Easily fatigued
Contraction Phase
1. Nerve pulse/impulse transmitted through
action potential

2. Acetylcholine is released at neural juncture

3. Action potential transmitted to muscle fiber
via the T-tubles to the sarcoplasmic reticulum
(SR)
Contraction phase
4. Calcium is released from SR into
sarcoplasm

5. Calcium binds to troponin

6. ATP is hydrolyzed (burned)

7. Energy causes a shift in tropomyosin and
actin binding site is exposed
Contraction phase
8. Actin-myosin cross bridge forms (cross
bridge is termed actomyosin)

9. ATP hydrolyzed

10. Myosin head rotates

11. Repeated over and over; filaments slide
causing shortening of sarcomere
Contraction
A sarcomere contracting
Notice that neither filament
changes length
ACTIN MYOSIN
http://www.unmc.edu/Physiology/Mann/
mann14.html
http://www.blackwellpublishing.com/matt
hews/myosin.html
http://entochem.tamu.edu/musclestrucco
ntractswf/index.html
Relaxation phase
1. Acetylcholinesterase is released (neutralizes
acetylcholine)

2. Calcium pump activated by SR to sequester
calcium

3. Actin-myosin cross bridge terminated

4. Tropomyosin shifts covering the binding site
on actin
Relaxation phase
5. Passive sliding of filaments

6. Sarcomere returns to resting state
Be Able To:
• Draw a sarcomere showing:
Myosin
Actin
Z Line
A Band
I Band
H Zone
M Line
• Explain how a muscle contracts and relaxes
– starting with a nerve impulse and including the SR role
• Explain the role of ATP in muscle contraction and relaxation
•(See p.889-900 In The Meat We Eat)

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muscle physiology.pptx

Editor's Notes

  1. A- = non-difusable anions proteins and peptides