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MUSCULAR TISSUE
DR.G.NIMOSHINI
Post graduate student
Department of Oral Pathology & Microbiology
SRM Dental College,
Ramapuram, Chennai, India
INTRODUCTION
• Latin –musculus
(mouse).
• Mice moving under the
skin.
• Greek-sarco(flesh).
• Over 700 skeletal
muscles.
• Distributed almost
everwhere in the body.
Muscle
• Derived from mesoderm , by modification of
cells into muscle fibres.
Muscle tissue
SPECIAL TERM
• Used for the various
cytoplasmic organelles of
the muscle fibers
• Plasma membrane-
sarcolemma
• Cytoplasm-sarcoplasm
• Smooth endoplasmic
reticulum-sarcoplasmic
reticulum
• Mitochondira-sarcosomes
Muscular System Functions
• Body movement
• Maintenance of posture
• Respiration
• Production of body heat
• Communication
• Constriction of organs and vessels
• Heart beat
Properties of Muscle
• Excitability
– Capacity of muscle to respond to a stimulus
• Contractility
– Ability of a muscle to shorten with force
• Extensibility
– Muscle can be stretched to its normal resting length and
beyond to a limited degree
• Elasticity
– Ability of muscle to recoil to original resting length after
stretched
Classification of muscles
Contractile cell functioning as Multicellular contractile units
Muscle Tissue Types
• Skeletal
– Attached to bones
– Nuclei multiple and peripherally located
– Striated, Voluntary and involuntary (reflexes)
• Smooth
– Walls of hollow organs, blood vessels, eye, glands, skin
– Single nucleus centrally located
– Not striated, involuntary, gap junctions in visceral smooth
• Cardiac
– Heart
– Single nucleus centrally located
– Striations, involuntary, intercalated disks
Contractile cell functioning as single-
cell contractile units:
• Myoepithelial cells(found in association with
secretory acini)
• Myofibroblasts(involved in wound healing)
• Myoid cells(found around seminiferous
tubules)
• Pericytes(smooth muscle like cells that
surround blood vessels)
Skeletal Muscle Structure
• Muscle fibers or cells
– Develop from myoblasts
– Numbers remain
constant
• Connective tissue
• Nerve and blood vessels
STRUCTURE OF MUSCLE FIBER
• CT EPIMYSIUM:-
Encloses whole muscle
• CT PERIMYSIUM:-
Encloses each
fasciculus(bundle)
• CT ENDOMYSIUM:-
Encloses each muscle
fibres.
STRUCTURE OF MUSCLE FIBERS
Cylindrical in shape
Outside lies connective
tissue endomysium with
some fibroblasts, collagen
fibrils
• ,capillaries.
A. Skeletal muscle mass; B. Cross
section of muscle; C. One muscle
fasciculus
MUSCLE FIBRE
Cell membrane of fibre is sarcolemma
Cytoplasm of muscle is known as Sarcoplasm
Connective Tissue, Nerve,
Blood Vessels
• Connective tissue
– External lamina
– Endomysium
– Perimysium
– Fasciculus
– Epimysium
• Fascia
• Nerve and blood vessels
– Abundant
Parts of a Muscle
STRUCTURE EMBEDDED WITHIN
SARCOPLASM :-
• Nuclei
• Myofibril
• Golgi apparatus
• Mitochondria
• Sarcoplasm reticulum
• Ribosomes
• Glycogen
• Lipids
MYOFIBRIL & ITS MICROSCOPIC
STRUCTURE
SARCOMERE
 STRUCTURAL AND
FUNCTIONAL UNIT OF
SKELETAL MUSCLE.
EXTENDS BETWEEN
TWO Z LINES.
ELECTRON MICROSCOPIC STUDY OF
SARCOMERE
• Sarcomere consists of
thread known as
myofilaments.
• They are of two types:-
• ACTIN
• FILAMENT(THIN)
• MYOSIN
FILAMENT(THICK)
Structure of Actin and Myosin
CONTRACTILE ELEMENTS OF MUSCLE
• Myosin filaments
formed by myosin
molecules
• Actin filaments are
formed by three types
of protein:-
I. Actin
II. Tropomyosin
III.Troponin
MYOSIN FILAMENT
• Each myosin molecule
made up of 6
polypeptide chain,2
heavy chains and 4 light
chains.
PORTION OF MYOSIN
MOLECULE:-
1. TAIL PORTION
2. HEAD PORTION
MYOSIN MOLECULE
• Myosin molecule formed by two heavy chains
and four light chains of polypeptides
ACTIN MOLECULE
• The major constituents of the thin actin filaments.
• Each actin molecule is called F-actin and it is the
polymer of a small protein known as G-actin
• Actin molecules in the actin filament are arranged in
the form of a double helix.
• Each F actin molecule has an active site to which the
myosin head is attached
TROPONIN
• FORMED BY THREE
SUBUNITS:-
TROPONIN I:- attached
to F actin
TROPONIN T:- attached
to Tropomyosin
TROPONIN C:- attached
to calcium ions.
TROPOMYOSIN
• About 40 to 60 Tropomyosin molecules are
situated along the double helix strand of actin
filament.
• In relaxed condition of the muscle, the
Tropomyosin molecules cover all the active sites
of F actin molecules.
OTHER PROTEINS OF MUSCLE:-
• ACTININ
• DESMIN
• NEBULIN
• TITIN
• DYSTROPHIN
SARCOTUBULAR SYSTEM
• System of membranous
structures in the form of vesicles
and tubules in the sarcoplasm of
the muscle fibres
• Formed mainly by two types of
structures:
1. T tubules :-T tubules or
transverse tubules are narrow
tubules formed by the
invagination of the sarcolemma
2. L tubules or sarcoplasmic
reticulum:-Ltubules or
longitudinal tubules are the
closed tubules that run in long
axis of the muscle fiber
FUNCTION OF SARCOTUBULAR
SYSTEM
Function of T-Tubules
• responsible for rapid transmission of impulse in
the form of action potential from sarcolemma to
the myofibrils.
Function of L-Tubules
• L-tubules store a large quantity of calcium ions.
• When action potential reaches the cisternae of L-
tubule, the calcium ions are released into the
sarcoplasm.
Molecular basis of muscular
contraction
Includes three stages:-
• Excitation-contraction coupling
• Role of troponin and Tropomyosin
• Sliding Mechanism
EXCITATION CONTRACTION COUPLING
• Excitation-contraction
coupling is the process
that occurs in between
the excitation and
contraction of the
muscle.
Role of Troponin and Tropomyosin
SLIDING MECHANISM
Components of Sarcomeres
Sliding Filament Model
• Actin myofilaments sliding over myosin to
shorten sarcomeres
– Actin and myosin do not change length
– Shortening sarcomeres responsible for skeletal
muscle contraction
• During relaxation, sarcomeres lengthen
SLIDING MECHANISM
Sarcomere Shortening
SEQUENCE OF MUSCLE RELAXATION:-
SPECIAL STAINS
VAN GIESON – YELLOW MASSON TRICHOME - RED
PTAH - BLUE PAS – PALE PINK
METHENAMINE SILVER – PALE
GREY H AND E – DEEP PINK
L.S STRIATED MUSCLE –H& E C.S OF STRAITED MUSCLE – H& E
GROWTH AND REGENERATION
CELLS THAT FORM
SKELETAL MUSCLE ARE
CALLED MYOBLASTS
SATELLITE CELLS SERVES
AS A POTENTIAL
SOURCE OF NEW
MYOBLAST THAT ARE
CAPABLE OF FUSING
NEW MUSCLE FIBRE.
Smooth muscles
• Elongated spindle-shaped
muscle
• 30um in length
• Non striated,involuntary
• Supplied by autonomic
nerves system.
• MYOFIBRILS AND
SARCOMERE ARE ABSENT.
Smooth Muscle
• Characteristics
– Not striated
– Dense bodies instead of Z disks as in skeletal muscle
• Have non contractile intermediate filaments
– Ca2+ required to initiate contractions
• Types
– Visceral or unitary
• Function as a unit
– Multiunit
• Cells or groups of cells act as independent units
STRUCTURE IN WHICH SMOOTH
MUSCLES ARE PRESENT
Functional Properties of Smooth
Muscle
• Some visceral muscle exhibits autorhythmic
contractions
• Tends to contract in response to sudden
stretch but no to slow increase in length
• Exhibits relatively constant tension: Smooth
muscle tone
• Amplitude of contraction remains constant
although muscle length varies
Smooth Muscle Regulation
• Innervated by autonomic nervous system
• Neurotransmitter are acetylcholine and
norepinephrine
• Hormones important as epinephrine and
oxytocin
• Receptors present on plasma membrane
which neurotransmitters or hormones bind
determines response
CONTRACTILE PROTEINS
• ACTIN
• MYOSIN
• TROPOMYOSIN
• THICK AND THIN FILAMENTS
• Thick filaments formed by myosin molecule
• Thin filament formed by actin and
Tropomyosin molecule.
SARCOTUBULAR SYSTEM
• T – Tubules are absent.
• L – tubules are poorly developed
TYPES OF SMOOTH MUSCLE:-
SINGLE UNIT OR VISCERAL SMOOTH MUSCLE
Fibres with interconnecting gap junction.
Gap junctions allow rapid spread of action
potential throughout the tissue.
DISTRIBUTION OF SINGLE UNIT SMOOTH MUSCLE
FIBERS
Gastrointestinal organs
Uterus
Ureters
Respiratory tract.
MULTIUNIT SMOOTH MUSCLE
FIBERS:-
 MUSCLE FIBER WITHOUT INTERCONNECTING GAP JUNCTION.
DISTRIBUTION OF MULTIUNIT SMOOTH MUSCLE
FIBERS:-
• Ciliary muscle of eye
• Iris of the eye
• Nictitating membrane
• Arrector pili
• Smooth muscle of blood vessel and urinary bladder.
MOLECULAR BASIS OF SMOOTH
MUSCLE CONTRACTION:-
• This process is called
LATCH – BRIDGE
mechanism.
CONTROL OF SMOOTH MUSCLE
• NERVOUS FACTOR:-Sympathetic and parasympathetic
nerves control the activities.
• HUMORAL FACTOR:-Activity controlled by hormones ,
neurotransmitter and other humoral factor.
 HORMONES AND NEUROTRANSMITTER :acetyl
choline, ADH, Adrenaline, noradrenaline,
histamine.
 HUMORAL FACTORS CAUSES RELAXATION:
Lack of oxygen, excess of carbon dioxide , lactic acid ,
excess of potassium ion , decrease in calcium ion.
Cardiac muscle
• The heart wall is made
up of myocardium.
Cardiac muscle/myocardium
• Many similar structural and functional
characteristics of skeletal and smooth muscles.
• Exhibits cross strations.
• Shorter muscle fibers.
• Shows branching pattern.
• One or two nuclei placed centrally
• Involuntary and contracts automatically like
smooth muscle
FUNCTIONAL SYNCITIUM
• Darkly stained T lines across
the fibers –intercalated
discs
• Specialised cell junctions
between the ends of
adjacent muscle fibers.
• This cell junctions(gap
junction and desmosomes).
• Providing cytoplasmic
continuity.
• Rapid trasmission of
impluse.
• Contract simultaneously.
PURKINJE FIBRES
• The conducting system
of the heart.
• Modified cardiac
muscle fiber.
• Thicker ,larger, few
myofilaments.
• Conduct stimuli faster
(2-3m/s vs 0.6m/s).
• Seen beneath the
endocardium.
Four properties of cardiac cells
• EXITABILITY:
• CONDUCTIVITY:
• CONTRACTILITY:
• RHYTHMICITY:
STRUCTURE EMBEDDED WITHIN
SARCOPLASM :-
IHC MARKER FOR MUSCLES
• SMOOTH MUSCLE:- H.CAL DESMON,SMOOTH
MUSCLE SPECIFIC ACTIN
• SKELETAL MUSCLE :- INTEGRIN β1-d,FILAMIN
–C (FLN-C)/ACTIN BINDING LIKE
PROTEIN, ACTIN α-1 SKELETAL MUSCLE
• CARDIAC MUSCLE :- INTEGRIN β 1-d,
,FILAMIN –C (FLN-C)/ACTIN BINDING LIKE
PROTEIN.
MUSCULAR DYSTROPHY
• Genetic disorder causes weakness in the
muscle.
• Diagnosed by muscular biopsy.
• Individuals with MD donot produce
dystrophin.
Duchenne’s muscular dystrophy
• Most common type.
• Caused by a defect with the gene that makes a
protein – dystrophin.
• Without the protein, the muscles break down.
• And the person gradually becomes weaker.
• Symptoms:wasting of muscles,poor
balance,limited range of movements.
Becker muscular dystrophy
Becker muscular dystrophy
REFERENCES
• TEXT BOOK OF HISTOLOGY-A PRACTICAL GUIDE-second
edition , J P Gunasegaran.
• KRAUSE’S ESSENTIAL HUMAN HISTOLOGY FOR MEDICAL
STUDENTS -Third Edition ,William J. Krause, Ph.D.
• HAM’S HISTOLOGY – Ninth edition ,David H. Cormack
,Ph.D .
• WHEATHER’S FUNCTIONAL HISTOLOGY – 5th Edition ,
Young ,Lowe ,Stevens ,Health .
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Muscular tissue

  • 1. MUSCULAR TISSUE DR.G.NIMOSHINI Post graduate student Department of Oral Pathology & Microbiology SRM Dental College, Ramapuram, Chennai, India
  • 2.
  • 3. INTRODUCTION • Latin –musculus (mouse). • Mice moving under the skin. • Greek-sarco(flesh). • Over 700 skeletal muscles. • Distributed almost everwhere in the body.
  • 4.
  • 5. Muscle • Derived from mesoderm , by modification of cells into muscle fibres.
  • 7. SPECIAL TERM • Used for the various cytoplasmic organelles of the muscle fibers • Plasma membrane- sarcolemma • Cytoplasm-sarcoplasm • Smooth endoplasmic reticulum-sarcoplasmic reticulum • Mitochondira-sarcosomes
  • 8.
  • 9.
  • 10. Muscular System Functions • Body movement • Maintenance of posture • Respiration • Production of body heat • Communication • Constriction of organs and vessels • Heart beat
  • 11.
  • 12. Properties of Muscle • Excitability – Capacity of muscle to respond to a stimulus • Contractility – Ability of a muscle to shorten with force • Extensibility – Muscle can be stretched to its normal resting length and beyond to a limited degree • Elasticity – Ability of muscle to recoil to original resting length after stretched
  • 13. Classification of muscles Contractile cell functioning as Multicellular contractile units
  • 14. Muscle Tissue Types • Skeletal – Attached to bones – Nuclei multiple and peripherally located – Striated, Voluntary and involuntary (reflexes) • Smooth – Walls of hollow organs, blood vessels, eye, glands, skin – Single nucleus centrally located – Not striated, involuntary, gap junctions in visceral smooth • Cardiac – Heart – Single nucleus centrally located – Striations, involuntary, intercalated disks
  • 15. Contractile cell functioning as single- cell contractile units: • Myoepithelial cells(found in association with secretory acini) • Myofibroblasts(involved in wound healing) • Myoid cells(found around seminiferous tubules) • Pericytes(smooth muscle like cells that surround blood vessels)
  • 16. Skeletal Muscle Structure • Muscle fibers or cells – Develop from myoblasts – Numbers remain constant • Connective tissue • Nerve and blood vessels
  • 17.
  • 18. STRUCTURE OF MUSCLE FIBER • CT EPIMYSIUM:- Encloses whole muscle • CT PERIMYSIUM:- Encloses each fasciculus(bundle) • CT ENDOMYSIUM:- Encloses each muscle fibres.
  • 19. STRUCTURE OF MUSCLE FIBERS Cylindrical in shape Outside lies connective tissue endomysium with some fibroblasts, collagen fibrils • ,capillaries. A. Skeletal muscle mass; B. Cross section of muscle; C. One muscle fasciculus
  • 20. MUSCLE FIBRE Cell membrane of fibre is sarcolemma Cytoplasm of muscle is known as Sarcoplasm
  • 21. Connective Tissue, Nerve, Blood Vessels • Connective tissue – External lamina – Endomysium – Perimysium – Fasciculus – Epimysium • Fascia • Nerve and blood vessels – Abundant
  • 22. Parts of a Muscle
  • 23. STRUCTURE EMBEDDED WITHIN SARCOPLASM :- • Nuclei • Myofibril • Golgi apparatus • Mitochondria • Sarcoplasm reticulum • Ribosomes • Glycogen • Lipids
  • 24. MYOFIBRIL & ITS MICROSCOPIC STRUCTURE
  • 25. SARCOMERE  STRUCTURAL AND FUNCTIONAL UNIT OF SKELETAL MUSCLE. EXTENDS BETWEEN TWO Z LINES.
  • 26. ELECTRON MICROSCOPIC STUDY OF SARCOMERE • Sarcomere consists of thread known as myofilaments. • They are of two types:- • ACTIN • FILAMENT(THIN) • MYOSIN FILAMENT(THICK)
  • 27. Structure of Actin and Myosin
  • 28. CONTRACTILE ELEMENTS OF MUSCLE • Myosin filaments formed by myosin molecules • Actin filaments are formed by three types of protein:- I. Actin II. Tropomyosin III.Troponin
  • 29. MYOSIN FILAMENT • Each myosin molecule made up of 6 polypeptide chain,2 heavy chains and 4 light chains. PORTION OF MYOSIN MOLECULE:- 1. TAIL PORTION 2. HEAD PORTION
  • 30. MYOSIN MOLECULE • Myosin molecule formed by two heavy chains and four light chains of polypeptides
  • 31. ACTIN MOLECULE • The major constituents of the thin actin filaments. • Each actin molecule is called F-actin and it is the polymer of a small protein known as G-actin • Actin molecules in the actin filament are arranged in the form of a double helix. • Each F actin molecule has an active site to which the myosin head is attached
  • 32. TROPONIN • FORMED BY THREE SUBUNITS:- TROPONIN I:- attached to F actin TROPONIN T:- attached to Tropomyosin TROPONIN C:- attached to calcium ions.
  • 33. TROPOMYOSIN • About 40 to 60 Tropomyosin molecules are situated along the double helix strand of actin filament. • In relaxed condition of the muscle, the Tropomyosin molecules cover all the active sites of F actin molecules.
  • 34. OTHER PROTEINS OF MUSCLE:- • ACTININ • DESMIN • NEBULIN • TITIN • DYSTROPHIN
  • 35. SARCOTUBULAR SYSTEM • System of membranous structures in the form of vesicles and tubules in the sarcoplasm of the muscle fibres • Formed mainly by two types of structures: 1. T tubules :-T tubules or transverse tubules are narrow tubules formed by the invagination of the sarcolemma 2. L tubules or sarcoplasmic reticulum:-Ltubules or longitudinal tubules are the closed tubules that run in long axis of the muscle fiber
  • 36. FUNCTION OF SARCOTUBULAR SYSTEM Function of T-Tubules • responsible for rapid transmission of impulse in the form of action potential from sarcolemma to the myofibrils. Function of L-Tubules • L-tubules store a large quantity of calcium ions. • When action potential reaches the cisternae of L- tubule, the calcium ions are released into the sarcoplasm.
  • 37. Molecular basis of muscular contraction Includes three stages:- • Excitation-contraction coupling • Role of troponin and Tropomyosin • Sliding Mechanism
  • 38. EXCITATION CONTRACTION COUPLING • Excitation-contraction coupling is the process that occurs in between the excitation and contraction of the muscle.
  • 39. Role of Troponin and Tropomyosin
  • 42. Sliding Filament Model • Actin myofilaments sliding over myosin to shorten sarcomeres – Actin and myosin do not change length – Shortening sarcomeres responsible for skeletal muscle contraction • During relaxation, sarcomeres lengthen
  • 45. SEQUENCE OF MUSCLE RELAXATION:-
  • 46. SPECIAL STAINS VAN GIESON – YELLOW MASSON TRICHOME - RED
  • 47. PTAH - BLUE PAS – PALE PINK
  • 48. METHENAMINE SILVER – PALE GREY H AND E – DEEP PINK
  • 49. L.S STRIATED MUSCLE –H& E C.S OF STRAITED MUSCLE – H& E
  • 50. GROWTH AND REGENERATION CELLS THAT FORM SKELETAL MUSCLE ARE CALLED MYOBLASTS SATELLITE CELLS SERVES AS A POTENTIAL SOURCE OF NEW MYOBLAST THAT ARE CAPABLE OF FUSING NEW MUSCLE FIBRE.
  • 51. Smooth muscles • Elongated spindle-shaped muscle • 30um in length • Non striated,involuntary • Supplied by autonomic nerves system. • MYOFIBRILS AND SARCOMERE ARE ABSENT.
  • 52. Smooth Muscle • Characteristics – Not striated – Dense bodies instead of Z disks as in skeletal muscle • Have non contractile intermediate filaments – Ca2+ required to initiate contractions • Types – Visceral or unitary • Function as a unit – Multiunit • Cells or groups of cells act as independent units
  • 53. STRUCTURE IN WHICH SMOOTH MUSCLES ARE PRESENT
  • 54. Functional Properties of Smooth Muscle • Some visceral muscle exhibits autorhythmic contractions • Tends to contract in response to sudden stretch but no to slow increase in length • Exhibits relatively constant tension: Smooth muscle tone • Amplitude of contraction remains constant although muscle length varies
  • 55. Smooth Muscle Regulation • Innervated by autonomic nervous system • Neurotransmitter are acetylcholine and norepinephrine • Hormones important as epinephrine and oxytocin • Receptors present on plasma membrane which neurotransmitters or hormones bind determines response
  • 56. CONTRACTILE PROTEINS • ACTIN • MYOSIN • TROPOMYOSIN • THICK AND THIN FILAMENTS • Thick filaments formed by myosin molecule • Thin filament formed by actin and Tropomyosin molecule.
  • 57. SARCOTUBULAR SYSTEM • T – Tubules are absent. • L – tubules are poorly developed
  • 58. TYPES OF SMOOTH MUSCLE:- SINGLE UNIT OR VISCERAL SMOOTH MUSCLE Fibres with interconnecting gap junction. Gap junctions allow rapid spread of action potential throughout the tissue. DISTRIBUTION OF SINGLE UNIT SMOOTH MUSCLE FIBERS Gastrointestinal organs Uterus Ureters Respiratory tract.
  • 59. MULTIUNIT SMOOTH MUSCLE FIBERS:-  MUSCLE FIBER WITHOUT INTERCONNECTING GAP JUNCTION. DISTRIBUTION OF MULTIUNIT SMOOTH MUSCLE FIBERS:- • Ciliary muscle of eye • Iris of the eye • Nictitating membrane • Arrector pili • Smooth muscle of blood vessel and urinary bladder.
  • 60. MOLECULAR BASIS OF SMOOTH MUSCLE CONTRACTION:- • This process is called LATCH – BRIDGE mechanism.
  • 61. CONTROL OF SMOOTH MUSCLE • NERVOUS FACTOR:-Sympathetic and parasympathetic nerves control the activities. • HUMORAL FACTOR:-Activity controlled by hormones , neurotransmitter and other humoral factor.  HORMONES AND NEUROTRANSMITTER :acetyl choline, ADH, Adrenaline, noradrenaline, histamine.  HUMORAL FACTORS CAUSES RELAXATION: Lack of oxygen, excess of carbon dioxide , lactic acid , excess of potassium ion , decrease in calcium ion.
  • 62.
  • 63. Cardiac muscle • The heart wall is made up of myocardium.
  • 64. Cardiac muscle/myocardium • Many similar structural and functional characteristics of skeletal and smooth muscles. • Exhibits cross strations. • Shorter muscle fibers. • Shows branching pattern. • One or two nuclei placed centrally • Involuntary and contracts automatically like smooth muscle
  • 65.
  • 66. FUNCTIONAL SYNCITIUM • Darkly stained T lines across the fibers –intercalated discs • Specialised cell junctions between the ends of adjacent muscle fibers. • This cell junctions(gap junction and desmosomes). • Providing cytoplasmic continuity. • Rapid trasmission of impluse. • Contract simultaneously.
  • 67. PURKINJE FIBRES • The conducting system of the heart. • Modified cardiac muscle fiber. • Thicker ,larger, few myofilaments. • Conduct stimuli faster (2-3m/s vs 0.6m/s). • Seen beneath the endocardium.
  • 68. Four properties of cardiac cells • EXITABILITY: • CONDUCTIVITY: • CONTRACTILITY: • RHYTHMICITY:
  • 70.
  • 71. IHC MARKER FOR MUSCLES • SMOOTH MUSCLE:- H.CAL DESMON,SMOOTH MUSCLE SPECIFIC ACTIN • SKELETAL MUSCLE :- INTEGRIN β1-d,FILAMIN –C (FLN-C)/ACTIN BINDING LIKE PROTEIN, ACTIN α-1 SKELETAL MUSCLE • CARDIAC MUSCLE :- INTEGRIN β 1-d, ,FILAMIN –C (FLN-C)/ACTIN BINDING LIKE PROTEIN.
  • 72. MUSCULAR DYSTROPHY • Genetic disorder causes weakness in the muscle. • Diagnosed by muscular biopsy. • Individuals with MD donot produce dystrophin.
  • 73.
  • 74. Duchenne’s muscular dystrophy • Most common type. • Caused by a defect with the gene that makes a protein – dystrophin. • Without the protein, the muscles break down. • And the person gradually becomes weaker. • Symptoms:wasting of muscles,poor balance,limited range of movements.
  • 75.
  • 76.
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  • 82.
  • 83. REFERENCES • TEXT BOOK OF HISTOLOGY-A PRACTICAL GUIDE-second edition , J P Gunasegaran. • KRAUSE’S ESSENTIAL HUMAN HISTOLOGY FOR MEDICAL STUDENTS -Third Edition ,William J. Krause, Ph.D. • HAM’S HISTOLOGY – Ninth edition ,David H. Cormack ,Ph.D . • WHEATHER’S FUNCTIONAL HISTOLOGY – 5th Edition , Young ,Lowe ,Stevens ,Health .