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There are three main types…
1-Slow Twitch Fibres 2-Fast Twitch Fibres 3-Very
Fast Twitch Fibres
These types produce different degrees of force due to slight
differences in the characteristics of how they work.
A- SLOW TWITCH FIBRES:
They contract slowly but can contract repeatedly over long
periods.
They have a good blood supply. Hence they are "RED
FIBRES ".
Suited to endurance activity using the aerobic energy
system which relies on Oxygen from the blood for the
supply of energy.
They are smaller and develop less force than fast twitch
SKELETAL MUSCLE:
TYPES OF SKELETAL MUSCLE
FIBRES:
B- FAST TWITCH FIBRES:
They have fast contraction speed and can use
aerobic(Oxygen dependant) energy sources as well as
anaerobic(Oxygen Indepedent) energy sources. They
are WHITE FIBRES. As they are less reliant on
Oxygen supplied by blood for energy and therefore
Fatigue Faster than slow twitch fibres.
Suited to speed, strength and power type activities.
Such as:
moderately heavy weight training and fast running
events such as 400 meters.
C- VERY FAST TWITCH FIBRES:
They contract extremely rapidly. They create very
forceful muscle contractions and fatigue quickly. They
are also " WHITE FIBRES " but unlike fast fibres.
They can only use anaerobic energy sources.
They also suited to speed, strength and power type
Q : What determines how many muscle fibre type an
individual has?
Ans: 1-Genetics 2-Hormone levels within
blood
3-Training undertaken
GENETICS: It is based on parent’s genes genetically
programmed to have certain percentage of each fibre.
The average person is born with around 60% fast twitch
and 40% slow twitch fibres(some persons may have larger
amounts of these fibres and therefore be more sui
TRAINING UNDERTAKEN: The ability to change the
fibre type is a common area of debate amongst exercise
physiologists. There is no evidence as yet to show that
fibre type can b changed.
However there is evidence to show that fibres adapt to the
type of training they are exposed to.
For Example:
If a person with predominantly slow twitch ′endurance ′
CHARACTERISTICS ARE SUMMARISED IN THE FOLLOWING TABLE
CHARACTERISTICS TYPE I TYPE II A TYPE II B
CONTRACTION SPEED
(mili seconds)
SLOW(90-140)
ms
FAST(50-100)
ms
VERY FAST(40-90)
ms
SIZE OF MOTOR
NEUTRONS(BIGGER
MOTOR NEUTRONS
ALLOW NERVE
IMPULSES TO
OPERATE MORE
QUICKLY)
SMALL LARGE VERY LARGE
RESISTANCE TO
FATIGUE
HIGH INTERMEDIATE LOW
ACTIVITY USED FOR ENDURANCE
TYPE ACTIVITIES
SHORT(<2 min)
HIGH INTENSITY
ACTIVITIES
VERY SHORT(1-30
sec) MAXIMAL
INTENSITY
ACTIVITIES
FORCE PRODUCTION LOW HIGH VERY HIGH
CHARACTERISTICS TYPE I TYPE II A TYPE II B
EFFICIENCY HIGH MEDIUM LOW
NO. OF MITOCHONDRIA
(IN MUSCLE FIBRES
PRODUCE ENERGY
AEROBICALLY)
HIGH MEDIUM LOW
CAPILLARY
DENSITY(TRANSPORT OF
OXYGEN AND NUTRIENT
TO MUSCLE AND
REMOVE WASTE
PRODUCTS)
HIGH INTERMEDIATE LOW
OXIDATIVE CAPACITY
(THE CAPACITY TO USE
OXYGEN FOR THE
PRODUCTION OF
ENERGY)
HIGH INTERMEDIATE LOW
MYOGLOBIN CONTENT
(A PIGMENT THAT
BINDS TO OXYGEN
GIVING THE FIBRE A
RED COLOUR)
HIGH MEDIUM LOW
GLYCOLYTIC CAPACITY
(TO STORE AND
BRAKEDOWN GLYCOGEN
FOR USE AS A HIGH
INTENSITY ENERGY
SOURCE)
LOW HIGH HIGH
ATPASE LEVELS
(IT IS AN ENZYME THAT
CONTROLS THE
BRAKEDOWN AND
SYNTHESIS OF ATP FOR
ENERGY)
LOW INTERMEDIATE HIGH
Connective tissue sheaths of skeletal muscle: epimysium, perimysium,
and endomysium.
Bone
Perimysium
Endomysium
(between individual
muscle fibers)
Muscle fiber
Fascicle
(wrapped by perimysium)
Epimysium
Tendon
Blood vessel
Fascicle
FIBRE
Muscle mass:
Muscle mass or muscle tissues are made up of a
large number of individual muscle cells.
The muscle cells are commonly called muscle fibers
because they are long and cylinder in appearance.
Fascia:
Muscle mass is
separated from the
neighboring tissues by a
thick fibrous tissue layer
known as fascia.
Epimysium:
Beneath the fascia
muscle is covered with a
connective tissue sheath
Fasciculi:
In the muscle the muscle fibers are arranged in
various groups called bundles or fasciculi.
Perimysium:
Connective tissue sheath that covers each
fasciculus is called perimysium.
Endomysium:
Each muscle fiber is covered by a connective
tissue layer called the endomysium.
Muscle fiber:
Each muscle cell or muscle fiber is cylindrical in
shape.
Average length of the fiber is 3cm. It varies
between 1cm to 4 cm, depending upon the length
of the muscle. The diameter of the muscle fiber
varies from 10µ to 100µ.
Each muscle fiber is enclosed by a cell membrane
called plasma membrane, that lies beneath the
endomysium called sarcolema.
Cytoplasm of the muscle is known as sarcoplasm.
The sarcolema consist of true cell membrane
called plasma membrane.
Structures embedded with in the sarcoplasm are;
1. Nuclie
2. Myofibril
Myofibrils:
Each muscle fiber itself contains cylindrical
organelles known as Myofibrils.
Myofibrils run through the entire length of the
muscle fiber, the myofibrils appear like small
distinct dots within the sarcoplasm.
In some muscle fibers, some of the myofibrils are
arranged in groups called cohnheim’s areas or
fields.
Surrounding the myofibrils there is a network of
tubules and channels called the Sarcoplasmic
reticulum.
Muscle contraction:
Is caused by interactions of thick and thin
filaments.
Structure of protein molecules determine its
interactions.
Each myofibril contains myofilaments:
Thick filaments:
A band contain thick filament(primarily composed of
myosin) is called as A band which:
Move closer together and Do not Shorten.
H band shorten:
Contain only myosin and Shorten during
contraction.
Thin filaments:
I band contains thin filaments(primarily composed
of actin) is called as I band which:
Decrease in length and it is a Distance between A
bands of successive Sarcomeres.
Center of each I band is Z disc.
Muscle Contracts because of sliding of thin
Sarcomere:
Z disc to Z disc.
M lines:
Produced by protein filaments in a sarcomere.
Anchor myosin during contraction.
Titin:
Elastic protein that runs through the myosin from M
line to Z disc.
Contributes to elastic recoil of muscle.
Microscopic anatomy of a skeletal
muscle fiber.
I band I bandA band
Sarcomere
H zone
Thin (actin)
filament
Thick (myosin)
filament
Z disc Z disc
M line
(c)Small part of one myofibril enlarged to show the myofilaments
responsible for the banding pattern. Each sarcomere extends from
one Z disc to the next.
Sliding filament theory:
Definition:
when a muscle contracts , the thin filaments slide
past the thick filaments, and the sarcomere
shortens. This process comprised of several steps
is called SLIDING FILAMENT THEORY. It is also
called WALK ALONG THEORY or the RACHET
THEORY.
Sliding of filaments is produced by the actions of
cross bridges.
Cross bridges:
Are part of the myosin proteins that extends out
towards actin. It form arms that terminate in heads.
Each myosin head contain an ATP binding site.
Contraction:
Myosin binding site splits ATP to ADP and Pi. ADP
and Pi remain bound to myosin until myosin heads
attach to actin.
Pi is released causing the power stroke to occur.
Power stroke pulls actin towards the center of the A
band. ADP is released when myosin binds to a fresh
ATP at the end of the power stroke. Release of ADP
upon binding to another ATP, causes the cross bridge
bond to break. Cross bridge detach, ready to bind
again.
Regulation of Contraction:
Regulation of cross bridge attachment to actin is due
to:
Tropomyosin:
Lies with in grove between double row of G-actin. In
relaxed muscle state Tropomyosin blocks binding sites
Role of Ca in Muscle Contraction:
Muscle Relaxation:
[Ca] in sarcoplasm lowers when tropomyosin blocks
attachment. Which prevents muscle contraction.
Ca is pumped back into the SR in the terminal
cisternae.
Na diffusion produces end-plate
potential(depolarization) + ions are attracted to
negative plasma membrane.
If depolarization sufficient, threshold occurs,
producing Action potential. This action potentials
travel down sarcolemma and T tubules.
Sarcoplasmic reticulum, terminal cisternae releases
Ca from chemical release channels. Ca is also
released through a Ca induced Ca release.
Ca attaches to troponin and Tropomyosin-troponin
Action Potential:
It is generated by increase in sodium ions in
sarcolemma.
That travels along the T tubules and leads to
excitation-contraction coupling.
Excitation-contraction coupling:
Action potential reaches a triad. Where releasing
calcium occur
This Triggering contraction requires myosin heads to be
in cocked position which is loaded by ATP energyConditions for skeletal muscle contraction:
There must be a neural stimulus. There must be
calcium in the muscle cell. ATP must be available for
energy.
So a few things can stop the contraction such as:
Energy system fatigue. Nervous system fatigue.
Voluntary nervous system control. Sensory nervous
Types of contraction:
1. Isotonic contraction 2. Isometric contraction
3. Eccentric contraction
In order for a muscle fiber to shorten they must
generate a force greater than the opposing forces
that act to prevent movement of that muscle
insertion.
Isotonic contraction:
Force of contraction remains constant through out
the shortening process.
Velocity of muscle shortening decreases as load
increases.
Isometric contraction:
Length of muscle fibers remain constant if the
number of muscle fibers activated is too few to
Upper neuron control of skeletal Muscle:
Cerebellum:
Receives sensory input from muscle spindles, golgi
tendon organs and areas of cerebral cortex devoted to
vision hearing and equilibrium. All output from
cerebellum is inhibitory
Disorders of Muscle Contraction:
Muscle Atrophy: It is characterized by weakening and
shrinking of a muscle. It may be caused by
immobilization and loss of neural stimulation.
Muscle Hypertrophy: It is characterized by
Enlargement of a muscle. Which leads to more
capillaries and more mitochondria.
It is caused by Strenous exercise as well as Steroid
hormones.
Tetany: Sustained contraction of a muscle
Result of a rapid succession of nerve impulse
A motor unit consists of a motor
neuron and all the muscle fibers it
innervates.
Spinal cord
Motor neuron
cell body
Muscle
Branching axon
to motor unit
Nerve
Motor
unit 1
Motor
unit 2
Muscle
fibers
Motor neuron
axon
Axon terminals at
neuromuscular junctions
Branching axon
terminals form
neuromuscular
junctions, one per
muscle fiber (photo-
micrograph 330x).
(b)
(a)
Motor Unit

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Skeletal muscle contraction

  • 1.
  • 2. There are three main types… 1-Slow Twitch Fibres 2-Fast Twitch Fibres 3-Very Fast Twitch Fibres These types produce different degrees of force due to slight differences in the characteristics of how they work. A- SLOW TWITCH FIBRES: They contract slowly but can contract repeatedly over long periods. They have a good blood supply. Hence they are "RED FIBRES ". Suited to endurance activity using the aerobic energy system which relies on Oxygen from the blood for the supply of energy. They are smaller and develop less force than fast twitch SKELETAL MUSCLE: TYPES OF SKELETAL MUSCLE FIBRES:
  • 3. B- FAST TWITCH FIBRES: They have fast contraction speed and can use aerobic(Oxygen dependant) energy sources as well as anaerobic(Oxygen Indepedent) energy sources. They are WHITE FIBRES. As they are less reliant on Oxygen supplied by blood for energy and therefore Fatigue Faster than slow twitch fibres. Suited to speed, strength and power type activities. Such as: moderately heavy weight training and fast running events such as 400 meters. C- VERY FAST TWITCH FIBRES: They contract extremely rapidly. They create very forceful muscle contractions and fatigue quickly. They are also " WHITE FIBRES " but unlike fast fibres. They can only use anaerobic energy sources. They also suited to speed, strength and power type
  • 4. Q : What determines how many muscle fibre type an individual has? Ans: 1-Genetics 2-Hormone levels within blood 3-Training undertaken GENETICS: It is based on parent’s genes genetically programmed to have certain percentage of each fibre. The average person is born with around 60% fast twitch and 40% slow twitch fibres(some persons may have larger amounts of these fibres and therefore be more sui TRAINING UNDERTAKEN: The ability to change the fibre type is a common area of debate amongst exercise physiologists. There is no evidence as yet to show that fibre type can b changed. However there is evidence to show that fibres adapt to the type of training they are exposed to. For Example: If a person with predominantly slow twitch ′endurance ′
  • 5. CHARACTERISTICS ARE SUMMARISED IN THE FOLLOWING TABLE CHARACTERISTICS TYPE I TYPE II A TYPE II B CONTRACTION SPEED (mili seconds) SLOW(90-140) ms FAST(50-100) ms VERY FAST(40-90) ms SIZE OF MOTOR NEUTRONS(BIGGER MOTOR NEUTRONS ALLOW NERVE IMPULSES TO OPERATE MORE QUICKLY) SMALL LARGE VERY LARGE RESISTANCE TO FATIGUE HIGH INTERMEDIATE LOW ACTIVITY USED FOR ENDURANCE TYPE ACTIVITIES SHORT(<2 min) HIGH INTENSITY ACTIVITIES VERY SHORT(1-30 sec) MAXIMAL INTENSITY ACTIVITIES FORCE PRODUCTION LOW HIGH VERY HIGH
  • 6. CHARACTERISTICS TYPE I TYPE II A TYPE II B EFFICIENCY HIGH MEDIUM LOW NO. OF MITOCHONDRIA (IN MUSCLE FIBRES PRODUCE ENERGY AEROBICALLY) HIGH MEDIUM LOW CAPILLARY DENSITY(TRANSPORT OF OXYGEN AND NUTRIENT TO MUSCLE AND REMOVE WASTE PRODUCTS) HIGH INTERMEDIATE LOW OXIDATIVE CAPACITY (THE CAPACITY TO USE OXYGEN FOR THE PRODUCTION OF ENERGY) HIGH INTERMEDIATE LOW
  • 7. MYOGLOBIN CONTENT (A PIGMENT THAT BINDS TO OXYGEN GIVING THE FIBRE A RED COLOUR) HIGH MEDIUM LOW GLYCOLYTIC CAPACITY (TO STORE AND BRAKEDOWN GLYCOGEN FOR USE AS A HIGH INTENSITY ENERGY SOURCE) LOW HIGH HIGH ATPASE LEVELS (IT IS AN ENZYME THAT CONTROLS THE BRAKEDOWN AND SYNTHESIS OF ATP FOR ENERGY) LOW INTERMEDIATE HIGH
  • 8. Connective tissue sheaths of skeletal muscle: epimysium, perimysium, and endomysium. Bone Perimysium Endomysium (between individual muscle fibers) Muscle fiber Fascicle (wrapped by perimysium) Epimysium Tendon Blood vessel Fascicle FIBRE
  • 9. Muscle mass: Muscle mass or muscle tissues are made up of a large number of individual muscle cells. The muscle cells are commonly called muscle fibers because they are long and cylinder in appearance. Fascia: Muscle mass is separated from the neighboring tissues by a thick fibrous tissue layer known as fascia. Epimysium: Beneath the fascia muscle is covered with a connective tissue sheath
  • 10. Fasciculi: In the muscle the muscle fibers are arranged in various groups called bundles or fasciculi. Perimysium: Connective tissue sheath that covers each fasciculus is called perimysium. Endomysium: Each muscle fiber is covered by a connective tissue layer called the endomysium.
  • 11. Muscle fiber: Each muscle cell or muscle fiber is cylindrical in shape. Average length of the fiber is 3cm. It varies between 1cm to 4 cm, depending upon the length of the muscle. The diameter of the muscle fiber varies from 10µ to 100µ. Each muscle fiber is enclosed by a cell membrane called plasma membrane, that lies beneath the endomysium called sarcolema. Cytoplasm of the muscle is known as sarcoplasm. The sarcolema consist of true cell membrane called plasma membrane. Structures embedded with in the sarcoplasm are; 1. Nuclie 2. Myofibril
  • 12. Myofibrils: Each muscle fiber itself contains cylindrical organelles known as Myofibrils. Myofibrils run through the entire length of the muscle fiber, the myofibrils appear like small distinct dots within the sarcoplasm. In some muscle fibers, some of the myofibrils are arranged in groups called cohnheim’s areas or fields. Surrounding the myofibrils there is a network of tubules and channels called the Sarcoplasmic reticulum.
  • 13.
  • 14. Muscle contraction: Is caused by interactions of thick and thin filaments. Structure of protein molecules determine its interactions.
  • 15. Each myofibril contains myofilaments: Thick filaments: A band contain thick filament(primarily composed of myosin) is called as A band which: Move closer together and Do not Shorten. H band shorten: Contain only myosin and Shorten during contraction. Thin filaments: I band contains thin filaments(primarily composed of actin) is called as I band which: Decrease in length and it is a Distance between A bands of successive Sarcomeres. Center of each I band is Z disc. Muscle Contracts because of sliding of thin
  • 16.
  • 17. Sarcomere: Z disc to Z disc. M lines: Produced by protein filaments in a sarcomere. Anchor myosin during contraction. Titin: Elastic protein that runs through the myosin from M line to Z disc. Contributes to elastic recoil of muscle.
  • 18. Microscopic anatomy of a skeletal muscle fiber. I band I bandA band Sarcomere H zone Thin (actin) filament Thick (myosin) filament Z disc Z disc M line (c)Small part of one myofibril enlarged to show the myofilaments responsible for the banding pattern. Each sarcomere extends from one Z disc to the next.
  • 19. Sliding filament theory: Definition: when a muscle contracts , the thin filaments slide past the thick filaments, and the sarcomere shortens. This process comprised of several steps is called SLIDING FILAMENT THEORY. It is also called WALK ALONG THEORY or the RACHET THEORY. Sliding of filaments is produced by the actions of cross bridges. Cross bridges: Are part of the myosin proteins that extends out towards actin. It form arms that terminate in heads. Each myosin head contain an ATP binding site.
  • 20.
  • 21. Contraction: Myosin binding site splits ATP to ADP and Pi. ADP and Pi remain bound to myosin until myosin heads attach to actin. Pi is released causing the power stroke to occur. Power stroke pulls actin towards the center of the A band. ADP is released when myosin binds to a fresh ATP at the end of the power stroke. Release of ADP upon binding to another ATP, causes the cross bridge bond to break. Cross bridge detach, ready to bind again. Regulation of Contraction: Regulation of cross bridge attachment to actin is due to: Tropomyosin: Lies with in grove between double row of G-actin. In relaxed muscle state Tropomyosin blocks binding sites
  • 22.
  • 23. Role of Ca in Muscle Contraction: Muscle Relaxation: [Ca] in sarcoplasm lowers when tropomyosin blocks attachment. Which prevents muscle contraction. Ca is pumped back into the SR in the terminal cisternae. Na diffusion produces end-plate potential(depolarization) + ions are attracted to negative plasma membrane. If depolarization sufficient, threshold occurs, producing Action potential. This action potentials travel down sarcolemma and T tubules. Sarcoplasmic reticulum, terminal cisternae releases Ca from chemical release channels. Ca is also released through a Ca induced Ca release. Ca attaches to troponin and Tropomyosin-troponin
  • 24. Action Potential: It is generated by increase in sodium ions in sarcolemma. That travels along the T tubules and leads to excitation-contraction coupling. Excitation-contraction coupling: Action potential reaches a triad. Where releasing calcium occur This Triggering contraction requires myosin heads to be in cocked position which is loaded by ATP energyConditions for skeletal muscle contraction: There must be a neural stimulus. There must be calcium in the muscle cell. ATP must be available for energy. So a few things can stop the contraction such as: Energy system fatigue. Nervous system fatigue. Voluntary nervous system control. Sensory nervous
  • 25. Types of contraction: 1. Isotonic contraction 2. Isometric contraction 3. Eccentric contraction In order for a muscle fiber to shorten they must generate a force greater than the opposing forces that act to prevent movement of that muscle insertion. Isotonic contraction: Force of contraction remains constant through out the shortening process. Velocity of muscle shortening decreases as load increases. Isometric contraction: Length of muscle fibers remain constant if the number of muscle fibers activated is too few to
  • 26.
  • 27. Upper neuron control of skeletal Muscle: Cerebellum: Receives sensory input from muscle spindles, golgi tendon organs and areas of cerebral cortex devoted to vision hearing and equilibrium. All output from cerebellum is inhibitory Disorders of Muscle Contraction: Muscle Atrophy: It is characterized by weakening and shrinking of a muscle. It may be caused by immobilization and loss of neural stimulation. Muscle Hypertrophy: It is characterized by Enlargement of a muscle. Which leads to more capillaries and more mitochondria. It is caused by Strenous exercise as well as Steroid hormones. Tetany: Sustained contraction of a muscle Result of a rapid succession of nerve impulse
  • 28. A motor unit consists of a motor neuron and all the muscle fibers it innervates. Spinal cord Motor neuron cell body Muscle Branching axon to motor unit Nerve Motor unit 1 Motor unit 2 Muscle fibers Motor neuron axon Axon terminals at neuromuscular junctions Branching axon terminals form neuromuscular junctions, one per muscle fiber (photo- micrograph 330x). (b) (a) Motor Unit