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Neuromuscular
Junction &
Muscle
Contraction
 Muscle fibers are muscle cells
Ensheathed by thin connective tissue layer called
endomysium
 Plasma membrane is called sarcolemma
 Muscle fibers are similar to other cells except are multinucleate
and striated
Skeletal Muscle Structure continued
12-6
Most distinctive feature of skeletal muscle is its
striations
Skeletal Muscle Structure continued
12-7
Neuromuscular Junction
12-8
Neuromuscular Junction (NMJ)
 Includes the single synaptic ending of the motor neuron
innervating each muscle fiber and underlying specializations of
sarcolemma
12-9
Place on sarcolemma where NMJ occurs is the motor
end plate
Neuromuscular Junction (NMJ) continued
12-10
Motor Unit
12-11
 Each motor
neuron branches
to innervate a
variable # of
muscle fibers
 A motor unit
includes each
motor neuron
and all fibers it
innervates
Motor Unit
12-12
When a motor neuron is activated, all muscle fibers in
its motor unit contract
Number of muscle fibers in motor unit varies according
to degree of fine control capability of the muscle
Innervation ratio is # motor neurons : muscle fibers
Vary from 1:100 to 1:2000
Fine control occurs when motor units are small, i.e.
1 motor neuron innervates small # of fibers
Motor Unit continued
12-13
Since individual motor units fire "all-or-none," how do
skeletal muscles perform smooth movements?
Recruitment is used:
Brain estimates number of motor units required
and stimulates them to contract
It keeps recruiting more units until desired
movement is accomplished in smooth fashion
More and larger motor units are activated to
produce greater strength
Motor Unit continued
12-14
Mechanisms of Contraction
12-15
Structure of Muscle Fiber
 Each fiber is packed with myofibrils
Myofibrils are 1µ in diameter and extend length of fiber
Packed with myofilaments
 Myofilaments are composed of thick and thin filaments
that give rise to bands which underlie striations
12-16
 A band is dark, contains
thick filaments (mostly
myosin)
Light area at center of
A band is H band
= area where actin
and myosin don’t
overlap
 I band is light, contains
thin filaments (mostly
actin)
At center of I band
is Z line/disc where
actins attach
Structure of Myofibril
12-17
12-18
 Are contractile units of skeletal muscle consisting of
components between 2 Z discs
 M lines are structural proteins that anchor myosin during
contraction
 Titin is elastic protein attaching myosin to Z disc that contributes
to elastic recoil of muscle
Sarcomeres
12-19
How Fiber Contracts
12-20
Sliding Filament Theory of Contraction
Muscle contracts because myofibrils get shorter
Occurs because thin filaments slide over and
between thick filaments towards center
Shortening distance from Z disc to Z disc
12-21
Sliding Filament Theory of Contraction continued
 During contraction:
 A bands (containing actin)
move closer together, do
not shorten
 I bands shorten because
they define distance
between A bands of
successive sarcomeres
 H bands (containing
myosin) shorten
12-22
12-23
Cross Bridges
 Are formed by heads of myosin molecules that extend toward
and interact with actin
 Sliding of filaments is produced by actions of cross bridges
Each myosin head contains an ATP-binding site which
functions as an ATPase
12-24
Cross Bridges continued
 Myosin can’t bind to actin unless it is “cocked” by ATP
After binding, myosin undergoes conformational change
(power stroke) which exerts force on actin
After power stroke myosin detaches
12-25
12-26
Control of Contraction
 Control of cross bridge attachment to actin is via troponin-
tropomyosin system
Serves as a switch for muscle contraction and relaxation
The filament tropomyosin lies in grove between double row
of G-actins (that make up actin thin filament)
Troponin complex is attached to tropomyosin at intervals of
every 7 actins
12-27
Control of Contraction continued
 In relaxed muscle,
tropomyosin blocks
binding sites on actin so
crossbridges can’t occur
This occurs when Ca++
levels are low
 Contraction can occur
only when binding sites
are exposed
12-28
Role of Ca++
in Muscle Contraction
When Ca++
levels rise, Ca++
binds to troponin causing
conformational change which moves tropomyosin and
exposes binding sites
Allowing crossbridges and contraction to occur
Crossbridge cycles stop when Ca++
levels decrease
12-29
Role of Ca++
in Muscle Contraction
 Ca++
levels decrease
because it is
continually pumped
back into the
sarcoplasmic
reticulum (SR - a
calcium reservoir in
muscle)
 Most Ca++
in SR is in
terminal cisternae
 Running along
terminal cisternae are
T tubules
12-30
Excitation-Contraction Coupling
 Skeletal muscle
sarcolemma is
excitable
Conducts Action
Potentials
 Release of ACh at
NMJ causes large
depolarizing end-plate
potentials and APs in
muscle
 APs race over
sarcolemma and
down into muscle via
T tubules
12-31
Excitation-Contraction Coupling continued
 T tubules are extensions
of sarcolemma
 Ca++
channels in SR are
mechanically linked to
channels in T tubules
 APs in T tubules cause
release of Ca++
from
cisternae via V-gated
and Ca++
release
channels
Called
electromechanical
release
channels are 10X
larger than V-gated
channels 12-32
Excitation-Contraction Coupling continued
12-33
Cardiac Muscle (Myocardium)
 Contractile apparatus similar to skeletal
 Striated like skeletal but involuntary like smooth
 Branched; adjacent myocardial cells joined by intercalated disks
(gap junctions)
Allow Action Potentials to spread throughout cardiac muscle
12-77

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Fox muscles

  • 1. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Neuromuscular Junction & Muscle Contraction
  • 2.  Muscle fibers are muscle cells Ensheathed by thin connective tissue layer called endomysium  Plasma membrane is called sarcolemma  Muscle fibers are similar to other cells except are multinucleate and striated Skeletal Muscle Structure continued 12-6
  • 3. Most distinctive feature of skeletal muscle is its striations Skeletal Muscle Structure continued 12-7
  • 5. Neuromuscular Junction (NMJ)  Includes the single synaptic ending of the motor neuron innervating each muscle fiber and underlying specializations of sarcolemma 12-9
  • 6. Place on sarcolemma where NMJ occurs is the motor end plate Neuromuscular Junction (NMJ) continued 12-10
  • 8.  Each motor neuron branches to innervate a variable # of muscle fibers  A motor unit includes each motor neuron and all fibers it innervates Motor Unit 12-12
  • 9. When a motor neuron is activated, all muscle fibers in its motor unit contract Number of muscle fibers in motor unit varies according to degree of fine control capability of the muscle Innervation ratio is # motor neurons : muscle fibers Vary from 1:100 to 1:2000 Fine control occurs when motor units are small, i.e. 1 motor neuron innervates small # of fibers Motor Unit continued 12-13
  • 10. Since individual motor units fire "all-or-none," how do skeletal muscles perform smooth movements? Recruitment is used: Brain estimates number of motor units required and stimulates them to contract It keeps recruiting more units until desired movement is accomplished in smooth fashion More and larger motor units are activated to produce greater strength Motor Unit continued 12-14
  • 12. Structure of Muscle Fiber  Each fiber is packed with myofibrils Myofibrils are 1µ in diameter and extend length of fiber Packed with myofilaments  Myofilaments are composed of thick and thin filaments that give rise to bands which underlie striations 12-16
  • 13.  A band is dark, contains thick filaments (mostly myosin) Light area at center of A band is H band = area where actin and myosin don’t overlap  I band is light, contains thin filaments (mostly actin) At center of I band is Z line/disc where actins attach Structure of Myofibril 12-17
  • 14. 12-18
  • 15.  Are contractile units of skeletal muscle consisting of components between 2 Z discs  M lines are structural proteins that anchor myosin during contraction  Titin is elastic protein attaching myosin to Z disc that contributes to elastic recoil of muscle Sarcomeres 12-19
  • 17. Sliding Filament Theory of Contraction Muscle contracts because myofibrils get shorter Occurs because thin filaments slide over and between thick filaments towards center Shortening distance from Z disc to Z disc 12-21
  • 18. Sliding Filament Theory of Contraction continued  During contraction:  A bands (containing actin) move closer together, do not shorten  I bands shorten because they define distance between A bands of successive sarcomeres  H bands (containing myosin) shorten 12-22
  • 19. 12-23
  • 20. Cross Bridges  Are formed by heads of myosin molecules that extend toward and interact with actin  Sliding of filaments is produced by actions of cross bridges Each myosin head contains an ATP-binding site which functions as an ATPase 12-24
  • 21. Cross Bridges continued  Myosin can’t bind to actin unless it is “cocked” by ATP After binding, myosin undergoes conformational change (power stroke) which exerts force on actin After power stroke myosin detaches 12-25
  • 22. 12-26
  • 23.
  • 24. Control of Contraction  Control of cross bridge attachment to actin is via troponin- tropomyosin system Serves as a switch for muscle contraction and relaxation The filament tropomyosin lies in grove between double row of G-actins (that make up actin thin filament) Troponin complex is attached to tropomyosin at intervals of every 7 actins 12-27
  • 25. Control of Contraction continued  In relaxed muscle, tropomyosin blocks binding sites on actin so crossbridges can’t occur This occurs when Ca++ levels are low  Contraction can occur only when binding sites are exposed 12-28
  • 26. Role of Ca++ in Muscle Contraction When Ca++ levels rise, Ca++ binds to troponin causing conformational change which moves tropomyosin and exposes binding sites Allowing crossbridges and contraction to occur Crossbridge cycles stop when Ca++ levels decrease 12-29
  • 27. Role of Ca++ in Muscle Contraction  Ca++ levels decrease because it is continually pumped back into the sarcoplasmic reticulum (SR - a calcium reservoir in muscle)  Most Ca++ in SR is in terminal cisternae  Running along terminal cisternae are T tubules 12-30
  • 28. Excitation-Contraction Coupling  Skeletal muscle sarcolemma is excitable Conducts Action Potentials  Release of ACh at NMJ causes large depolarizing end-plate potentials and APs in muscle  APs race over sarcolemma and down into muscle via T tubules 12-31
  • 29.
  • 30. Excitation-Contraction Coupling continued  T tubules are extensions of sarcolemma  Ca++ channels in SR are mechanically linked to channels in T tubules  APs in T tubules cause release of Ca++ from cisternae via V-gated and Ca++ release channels Called electromechanical release channels are 10X larger than V-gated channels 12-32
  • 32. Cardiac Muscle (Myocardium)  Contractile apparatus similar to skeletal  Striated like skeletal but involuntary like smooth  Branched; adjacent myocardial cells joined by intercalated disks (gap junctions) Allow Action Potentials to spread throughout cardiac muscle 12-77