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Muscle TissueThe muscle tissue is an assemblage of cells which
are highly specialized in contractility by virtue of their cellular contents of contractile structural
proteins.
The contractile ability of muscle cells is responsible
for movements in some organs and the body as awhole.
Muscle cells are derived from the embryonic
mesoderm through a process of cellular elongationaccompanied by intracellular synthesis of
myofibrilar proteins.
Muscle tissue is widely distributed all over the body.
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Classification of muscles (See Fig M1)
Muscle cells are classified into four main types
based on structural and functional properties of the
cells.These include:
1. Striated skeletal muscle: Striated skeletal muscleusually exist in bundles which are made up oflong, cylindrical and multinucleated cells. Theyalso posses cross striations under the lightmicroscope and are often attached to bones(skeleton). They are multinucleated and
voluntarily controlled2. Striated non-skeletal muscle: This muscle type
share the same properties with striated skeletalmuscle except that they are not attached to
bones and are not under voluntary control.
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3. Cardiac muscle: This muscle type also exists in
bundles, posses cross striations, long,
cylindrical, multinucleated and branching cells.
The cells (fibres) run parallel to one another and
are connected end-to-end by intercalated disks.
Cardiac muscles are not under voluntary control
and are restricted to the heart and some veins.4. Smooth Muscle: Smooth muscles are made up of
bundles of small, fusiform, and mononucleated
cell which have no cross striation under light
microscopic view. This muscle type is widelydistributed in the internal organs and is not
under voluntary control.
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Other Characteristic features of the
basic types of muscles are best
appreciated by a tabular
comparison of the muscles as
follows:
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Internal Organization of the Skeletal Muscle
(See Fig M3A & M3B):
• A skeletal muscle fibre may be up to 35 cm in length
with a diameter ranging from 10 to 100 micron
• Under the light microscope, a longitudinal section of a
skeletal muscle fibre show cross-striation which
comprises alternating dark and light bands.• The dark bands are referred to as the
A band (Anisotropic band) and
•
The Light band are the I band (Isotropic band).• Under the electron microscopic view, each I band is
divided in the middle by a transverse line called the
Z line.
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• The dark bands are also formed by Myosin
contractile proteins while the light bands are
formed by Actin contractile proteins.
• The contractile apparatus of the muscle is
subdivided into subunit referred to as the
SARCOMERE
• The distance from one Z line to the next one
constitutes the Sarcomere of the skeletal
muscle (See Diagram).
• Sarcomeres are also interconnected at the Z
line by the proteins α-actinin and desmin.
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• Under the electron microscope, the A band
is also divided in the middle by a transverse
line called the M Line. This is the region at
which adjacent myosin are interconnectedlaterally. It is also formed mainly by creatine
kinase a protein involved in the synthesis of
ATP.• There are two light zones on either side of
the M line. These collectively constitute the
H band within the A band.• In this region there is no overlap between
myosin and actin (See Fig. M3).
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Contractile Proteins of the Striated muscle
(See Fig. M4):
•
Myosin and Actin are the principal proteinsof the myofibrils constituting 55% of
myofibrillar proteins. (Ratio 1-6)
•
While Myosin forms the thick filaments,Actin forms the thin filament.
• Two other contractile proteins associated
with the thin filaments are:• Tropomyosin (40 nm long) and
• Troponin (Three globular subunits)
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The Tubular systems of the Skeletal Muscle
(See Fig. M5A & M5B):
The tubular systems of the striated musclecomprise the:
• The transverse (T) tubules: These are finger-
like invaginations of the sarcolemma whichform tubular network around the myofibril at
the junction the light and dark bands. They
serve as channels through which electricalimpulse is propagated from the exterior to
the interior of the muscle cell.
S l i R ti l t b l
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Sarcoplasmic Reticulum tubules:
• The smooth sarcoplasmic reticulum of the
muscle cell form terminal cisternae on either
side of the T tubular network leading to the
establishment of a system of three tubules
referred to as the Triad complex of tubules.
• The sarcoplasmic tubules contain calcium
ions which are released from the tubules on
stimulation by the impulse passing along
the T tubular network (See Diagram).
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I t l O i ti f th C di
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Internal Organization of the Cardiac
Muscle (See Fig. M6A & M6B):•
Cardiac muscle has an average diameter of 15µand length range of 85-100µ.
• Most cells are mononucleated but a few are
binucleated.
• In all cases the nuclei are centrally located.
• Cardiac muscle consists of branching muscle
fibres and adjacent fibres are connected end to
end via these branches by intercalated disks.• Intercalated disks are specialized junctional
complexes which are peculiar to cardiac muscle.
Th d f th t i
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They are made up of three components viz.
• Fasciae Adherentes which serve as anchoring
site for actin fibres
• Maculae Adherentes which bind cardiac muscle
fibres together and
•
Gap Junctions which provide channels for ionicand electric flow between cardiac muscle cells
(fibres).
• The arrangement of myofibrils in the cardiac
muscle is similar to the arrangement in skeletal
muscle.
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• Other Contents of the sarcoplasm of
cardiac muscle:
• Glycogen: This is the energy source of
the muscle and is stored in granules.
• Myoglobin: This is an oxygen binding
protein similar to hemoglobin in blood. It
imparts dark red color on the muscle
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Cardiac Tubular System:
•
The T-tubular systems are larger and morenumerous compared with skeletal muscle.
• However, only one sarcoplasmic reticulartubule is associated with the T-tubule thus a
diads tubular system is established in thecardiac muscular system.
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Other features of the sracoplasm of cardiac
muscle include:
• Abundance of mitochondria which constitute
40% of the sracoplasm
• Large deposit of fatty acids as glyceride as
the major fuel of cardiac muscle
• Small amount of glycogen
• Granules of lipofuscin pigments
1. Granules of the precursor of Atrial
natriuretic factor which is stored in large amount(around the nucleus) in the right atrium and less
quantity in other cardiac muscles.
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Internal Organization of the Smooth Muscle
(Fig. M7A & 7B)
•The length of the spindle shaped smoothmuscle cell varies from one organ to the other.
In the vascular wall it is about 20µ while in the
gravid uterus it could be as long as 500µ.• Smooth muscle cell is surrounded by a basal
lamina and a network of reticular fibres which
ensures that a bundle of smooth muscle
contract in unison.
• Smooth muscle lacks T-tubular system but
widely distributed sarcoplasmic reticulum.
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• The myofibrils which comprise myosin actin andtropomyosin are arranged in a crisscrosspattern.
• The contractile filaments are attached to focaldensities in the sracoplasm and to attachmentdensities on the sarcolemma.
•
The mechanism of contraction of actin andmyosin filament is similar to the mechanism inskeletal muscle.
• Intermediate filaments called desmin are also
found in the smooth muscle.• Electrical and ionic communication between
smooth muscle cells are effected through Nexus(Gap) junctions.
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Other sarcoplasmic contents of the smooth
muscle include:
• Calmodulin: This is a calcium binding
protein which forms a complex with calcium
ions. The complex so formed activates the
interaction between myosin and actin.
• Mitochondria
• Polyribosomes
• Rough endoplasmic reticulum
• Golgi complex
•
Pinocytotic vesicles
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Regeneration of muscle tissue:
• Striated skeletal and non-skeletal muscles
increase in size and number by proliferationof inactive myoblasts called satellite cells.
• Smooth muscles also regenerate from
mononucleated cells.• Cardiac muscles are incapable of
regeneration
The Neuromuscular Junction (See Fig M8):
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The Neuromuscular Junction (See Fig. M8):
• This is the contact point between the muscle and its
nerve supply. It is also referred to as the
Myoneuronal junction or Motor end plate:The principal features of this structure are:
• Demyelination of the synaptic bulb
•
Synaptic Cleft (gap) containing neurotransmitter • Synaptic junctional folds on the sarcolemma
• Presynaptic vesicles containing neurotransmitter
•
Pre and Post synaptic abundance of Mitochondria• Several nuclei, ribosomes and glycogen granules
beneath the junctional folds
• Neurotransmitter receptors on the sarcolemma
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