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PHYSIOLOGY

Muscle Physiology

PHYSIOLOGICAL ANATOMY OF SKELETAL M. ¨ Partially interdigitate causing alternating


light & dark bands7
– I bands – light, only actin, isotropic to
polarized light
– A bands – dark, myosin & ends of
actin, anisotropic to polarized light
¨ Z disc – ends of actin filaments attach here
– Actin extend in both directions to
interdigitate with myosin
– Made of filamentous proteins different
from actin & myosin
– Passes crosswise across myofibril &
crosswise from myofibril to myofibril

Titin Filaments
] Filamentous molecules of protein maintaining
the side-by-side relationship between myosin &
actin
] Very springy
] Act as framework holding myosin & actin in
place so contractile machinery of sarcomere will
work
] On one end, it is elastic & attached to Z disk
¨ Acts as spring & changes length as
sarcomere contracts & relaxes
] Other end tethers it to myosin thick filament
] May act as template for initial formation of
portions of contractile filaments of sarcomere,
especially myosin

Myofibril Muscle Fiber / Myofiber


] Each muscle fiber contains densely arranged ] Smallest unit of skeletal muscle is a
spiral array of cylindrical elements multinucleated, elongated cell
] Essentially an end-to-end chain of regular ] Enclosed by sarcolemma which fuses with a
repeating units or sarcomeres tendon fiber
¨ Portion of myofibril that lies between 2 ¨ Has true cell membrane (plasma)
successive Z discs ¨ Has outer coat of thin layer of
¨ When muscle fiber is contracted, length of polysaccharide material with thin collagen
sarcomere is 2 microm fibrils
– Actin completely overlap with myosin ] Surrounded by endomisium
& actin tips are beginning to overlap
one another Fascicle
] Composed of large, polymerized protein ] Bundle of linearly aligned muscled fibers
molecules responsible for muscle contraction
(myofilaments) Muscle
¨ Thick filaments are myosin ] Bundles of fascicle
¨ Thin filaments are actin

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Ella Alexa Calingasan-Abrogueña
PHYSIOLOGY
Muscle Physiology

Transverse Tubules
Sarcoplasmic Reticulum

] Action potentials spread to interior of muscle


fiber by way of transverse tubule
] Only in skeletal & cardiac
] Penetrate muscle fiber & surround myofibrils at
2 points in each sarcomere: A & I bands
] Are small & run transverse to myofibrils
] Begin at cell membrane & penetrate all the way ] 2 major parts
from one side of muscle fiber to opposite side ¨ Terminal cisternae – large chambers that
] Branch among themselves & form entire planes abut T tubules
of T tubules interlacing among all separate ¨ Long longitudinal tubules surrounding all
myofibrils surfaces of contracting myofibrils
] Where T tubules originate from cell membrane, ] Within its vesicular tubules is an excess of Ca+
they are open to exterior of muscle fiber in high concentration
] Communicate with ECF surrounding muscle ¨ Many are released from each vesicle when
fiber & contain ECF in their lumens AP occurs in adjacent T tubule
] When an AP spreads over a muscle fiber
membrane, potential change also spreads along T
tubules to deep interior of muscle fiber
] Electrical currents surrounding T tubules elicit
muscle contraction
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Ella Alexa Calingasan-Abrogueña
PHYSIOLOGY
Muscle Physiology

EXCITATION-CONTRACTION COUPLING
] T tubule AP cause the release of Ca+ in muscle
fiber in immediate vicinity of myofibrils
¨ Ca+ cause muscle contractions
] As AP reaches T tubule, voltage change is
sensed by dihydropyridine receptors (DHP)
linked to Ca+-release channels or ryanodine
receptor channels
] Activation of DHP triggers opening of Ca+-
release channels in cisternae & in attached
longitudinal tubules
¨ Channels remain open for few milliseconds
¨ Release Ca+ into sarcoplasm surrounding
myofibrils = contraction
] During repolarization, conformational change in
] Once Ca+ has been released from sarcoplasmic
DHP receptor closes Ca+ release channels
tubules & have diffused among myofibrils,
¨ Ca+ transported from sarcoplasm into SR
muscle contractions continue until Ca+
by ATP-dependent pump SERCA concentration remains high

Removal of Ca+
] May be extruded across cell plasma membrane
] Sequestered within intracellular compartments
] A continually active Ca+ pump in walls of SR
pumps Ca away from myofibril back into
sarcoplasmic tubules
] Inside SR is protein calsequestrin that can bind
to 40x more Ca
¨ Buffers Ca+ within SR lumen
¨ Unload Ca+ in vicinity of Ca+-release
channel = EC coupling
] Important pumps
¨ SERCA
¨ PMCA
¨ Na-Ca Exchanger

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Ella Alexa Calingasan-Abrogueña
PHYSIOLOGY
Muscle Physiology

MUSCLE CONTRACTION
AP travels along motor nerve to NMJ

Nerve secretes small amount of ACh

Opening of ACh gated cation channels

Diffusion of large quantities of Na+ ions
= local depolarization

Opening of voltage-gated Na+ channels
= initiation of AP at membrane

AP travels along muscle fiber & through center of
muscle fiber

SR releases large quantities of Ca+ that have been stored

Ca+ initiate attractive forces between actin & myosin
= slide alongside (contractile process)

Ca+ are pumped back to SR by Ca membrane pump
= ceases of muscle contraction

] Muscle contraction occurs by sliding filament


mechanism
] Myosin head has innate ATP activity

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Ella Alexa Calingasan-Abrogueña
PHYSIOLOGY
Muscle Physiology

ACTIN FILAMENT

] Composed of actin, tropomyosin, & troponin


] Troponin includes troponin I, C, & T
] Inhibited by troponin-tropomyosin complex
] Activation is brough by Ca+

CROSS-BRIDGING

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Ella Alexa Calingasan-Abrogueña
PHYSIOLOGY
Muscle Physiology

ISOTONIC vs ISOMETRIC twitch that is superimposed on residual tension


of initial twitch
¨ Activates greater isometric tension than the
first
] Adding individual twitch contractions to increase
intensity of overall muscle contraction
] If multiple AP occurs close enough in time, the
multiple features can summate & greatly increase
tension developed
] Summation is more effective at increasing
tension when AP are grouped more closely in
time

2 types
1. Multiple fiber summation
¨ Increasing number of motor units contracting
simultaneously
2. Frequency summation
Isometric Contraction ¨ Increasing frequency of contraction
] Attachment points are immobile, thereby fixing ¨ Can lead to tetanization
muscle length
] Stimulation causes an increase in tension but no Tetanization
shortening ] When frequency of contraction reaches a critical
level
Isotonic Contraction ] Successive contraction eventually become so
] One of 2 attachment points is mobile & force rapid that they fuse together
tends to pull this mobile point away from fixed ] Whole muscle contraction appears to be smooth
one & continuous
] Stimulation causes shortening, provided tension ] Cannot be maintained for long periods of time
developed by muscle is greater than opposing because of fatigue
load
Tetany
MUSCLE TWITCH ] Occurs because enough Ca+ are maintained in
muscle sarcoplasm, even between APs
] Contraction-relaxation of a skeletal muscle in ] Full contractile state is sustained without
response to single stimulus allowing any relaxation between APs
] When muscle is activated by single stimulus,
there is a brief lag/latent period
¨ Prior to initiation of tension development
] Rapid shortening or period of contraction
] Slightly longer period of relaxation

SUMMATION
] If a skeletal muscle is stimulated & a 2nd stimulus
is applied before initial contraction has fully
subsided, a 2nd contraction or AP induces a

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Ella Alexa Calingasan-Abrogueña
PHYSIOLOGY
Muscle Physiology

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Ella Alexa Calingasan-Abrogueña

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