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outstanding characteristic of muscle tissue
ability to shorten or contract
3 muscle tissue types
skeletal, cardiac, smooth
how are muscle tissue types classified?
structure, contractile props, location, and control mechanisms
skeletal muscle
most attached to bones (some attached to skin or other skeletal muscles)
contraction → skeleton movement
controlled by somatic division of nervous system
microscopic appearance: alternating transverse light and dark bands (striations)
VOLUNTARY CONTROL
cardiac muscle
heart wall
contraction → propels blood through circulatory system
control: autorhythmic - adjusted by autonomic NS and hormones
INVOLUNTARY CONTROL
microscope: striations, intercalated discs
smooth muscle
surrounds hollow organs and tubes
found as single Cs or in small groups
contraction → propulsion of luminal contents or flow regulation
controlled by autonomic NS, hormones, and intrinsic factors
INVOLUNTARY CONTROL
microscope = no striations (smooth)
Functions of muscular tissue
producing the body movements, stabilizing body, storing and moving substances within the body, and generating heat
Properties of muscular tissue
electrical excitability, contractility, extensibility, elasticity
electrical excitability
ability to recieve and respond to stimuli by action potential production
contractility
ability to shorten
extensibility
ability to stretch
elasticity
ability to recoil
What does skeletal muscle contain?
muscle fibers: individual muscle
CT: surrounds muscle fiber and whole muscle
blood vessels and nerves
Connective tissue components
1) layers surround and protecting (3 layers)
epimysium
perimysium
endomysium
2) fascia
deep fascia
superficial fascia
3) Skeletal Muscle Attachments
tendons
aponeurosis
Epimysium
CT that surrounds the ENTIRE muscle
Perimysium
CT that penetrates the muscle and separates and surrounds the muscle fibers into bundles of 10-100 fibers = “pascicles”
Endomysium
Thin CT extensions enveloping each muscle FIBER
Deep fascia
between neighboring muscles (carry nerves, blood vessels, etc.)
Superficial fascia
hypodermis, subcutaneous layer
between muscle and skin (adipose)
Tendons
white, fibrous cords of dense, regular CT that attach muscle to bone
Aponeurosis
sheet like layer of CT joining a muscle to the part that it moves
Specific names for the attachments of both ends of a skeletal muscle
origin and insertion
origin
the more STATIONARY bone to which the muscle is attached (head) (usually proximal)
Insertion
the more MOBILE end (of bone) (usually distal)
Myoblasts
the immature contractions giving rise to muscle c (fibers)
can divide
fuse
multinucleated mature muscle fiber (cannot divide)
satellite cs:
inactive myoblasts ass. with mature muscle fibers
have the potential to divide
increase # in young children
hypertrophy
enlargement of existing muscle fibers
accounts for muscle growth after birth in response to hGH (note - testosterone promotes further muscle fiber enlargement)
fibrosis
replacement of muscle fibers by fibrous scar tissue following damage
sarcolemma
plasma membrane
sarcoplasm
cytoplasm
T (transverse) tubules
in folding of sarcolemma; carries electrical current (charge) from surface to cell interior → Ca++ release from terminal cisternae
What is muscle fiber made up of?
Myofibrils
Sarcoplasmic reticulum
membranous sacs encircle myofibril; stores Ca++
Terminal cisternae
dilated sacs of SR alongside T-tubules
Triad
T-tubule + 2 terminal cisternae (on either side)
Contractile Elements
thick filaments
thin filaments
actin
tropomyosin
troponin
A Band
I Band
thick filaments
mainly made up of the contractile protein MYOSIN
large protein molecule with a globular head attached to a long tail
300 myosin molecules
tails: lie along long axis
heads: extend outwards (forms crossbridges)
myosin molecules in the 2 halves of each filament are oriented in opposite directions → all tails directed toward center (central area w no heads)
thin filaments
made up of the contractile protein ACTIN, plus proteins tropomyosin and troponin
actin
globular (G) actin subunits (contain myosin BINDING site)
G actin subunits are helically intertwined into a filament = F actin
tropomyosin
thread like protein extending end to end along the actin surface (1 per 7 G-actin subunits)
blocks myosin binding sites (active site) on actin
regulatory protein
Troponin
small protein bound to tropomyosin; can bind Ca++
regulatory protein
Striations
occur due to actin and myosin organization in skeletal and cardiac muscle
A bAnd = dArk band
thick filaments + overlapping think and thick filaments
H zone
M line
A band
extends entire length of thick filament
H zone
lighter region in middle of A band (o think fils)
M line
proteins at center of H zone (middle of sarcomere)
I Band
lIghter band, thin filaments only
Z-disc
Z-disc
narrow line bisecting I band
protein to which thin filaments are anchored
Sarcomere
compartmental arrangement of the filaments
each segment of myofibril from Z to Z
functional contractile unit of muscle fiber
Dystrophin significance
skeletal muscles also contain structural proteins (example - see relationship to muscular dystrophy)
Main Steps of Contraction of a Skeletal Muscle Fiber
nervous system excites a muscle fiber
excitation-contraction coupling (cross-bridging)
muscle CONTRACTION
muscle RELAXATION
Neuromuscular Junction
Synapse between the motor neuron (mn) and the muscle fiber
usually one per skeletal muscle
components of neuromuscular junction
motor neuron
motor end plate
cleft
motor neuron
(presynaptic membrane) somatic nerve cell supplying the neural stim for skeletal muscle fiber contraction
motor end plate (MEP)
region of fibers plasma membrane (sarcolemma), which lies directly under terminal portion of motor neuron axon - post synaptic membrane
cleft
separates the motor neuron and motor end plate
Excitation of a Skeletal Muscle Fibers Process
Release of Acetylcholine
Acetylcholine binds to acetylcholine receptors on fibers MEP
Production of Muscle Action Potential
Termination of Acetylcholine activity
What occurs at the release of acetylcholine stage of excitation?
motor neuron transmits electrical impulses
action potential reach the synaptic end bulb
acetylcholine molecules released from motor neuron ending by exocytosis
acetylcholine diffuse across gap (cleft)
What occurs at the Acetylcholine binds to Acetylcholine receptors on fibers MEP?
Na+ (sodium) channels open
What occurs during the production of the muscle action potential during the excitation process?
depolarization of plasma membrane at MEP (EPP) due to NA+ channels opening leads to electrical impulse (AP)
AP propagates (travels) along the membrane
AP initiates a series of intracellular events → the mechanical event of contraction
what occurs at the termination of ACh activity during the excitation of a skeletal muscle fiber?
breaking down acetylcholine
acetylcholinesterase
enzyme in cleft that breaks down Acetylcholine
slow acetylcholinesterase leads to an increase of acetylcholine in cleft which leads to increased muscle strength
Botulinum toxin
blocks exocytosis of acetylcholine from mn
curare
blocks acetylcholine receptors
Excitation Contraction Coupling
series of events by which a propagated action potential leads to thick and thin filament interaction
process of Excitation Contraction Coupling
propagated ap passes from the sarcolemma along the t-tubule
as the action potential passes along t-tubules it causes the opening of Calcium channels in the sarcoplasmic reticulum (SR) → Ca++ enters the cytosol
CA++ binds to troponin causing troponin to change shape
this conformation moves tropomyosin away from the myosin binding site on actin → cross-briding between thick and think filaments - > leads to muscle contraction
Contraction cycle
events that cause the filaments to slide
contraction cycle process
ATP hydrolysis
cross-bridges
power stroke
detachment of myosin from actin
ATP hydrolysis
energizes the myosin head
ATP → ADP + P
Cross-bridges
myson head attaches to actin
power stroke
cross-bridges rotate toward center of sarcomere
what causes detachment of myosin from actin
due to ATP binding
sliding filament theory
1. myosin cross bridges with actin 2. (ADP and P1 released) myosin power strokes (pulls towards the M line of sarcomere) 3. once new ATP attaches to myosin -> cross bridge detaches 4. atp breaks down into adp and p1 to allow the myosin to attach to an actin again
load
force exerted by the object (against tension)
Relaxation
why contraction doesn’t continue indefinitely
Ca++ions free in the cytosol for only a short time
Ca++ actively pumped back into SR (see again how ATP is needed for relaxation) → troponin strengthens attachment w/ actin → tropomyosin moves back into blocking position until another AP arrives causing Ca++ release
muscle metabolism
amount within fibers at the start of contractile activity is small
if a muscle fiber is to sustain contractile activity, more ATP must be produced
ATP
immediate energy source
3 ways a muscle fiber can form ATP
phosphorylation of ADP by creatine phosphate (CP) (unique to muscle fibers)
oxidation phosphorylation of ADP in the mitochondria (aerobic metabolism)
Substrate phosphorylation of ADP (anaerobic metabolism)
Creatine phosphate
Immediate Energy
phosphorylation of ADP by CP = rapid means of forming ATP
CP + ADP ← → Creatine + ATP
creatine kinase (CK) catalyzes reaction
provides only enough ATP to support muscle contraction during strenuous exercise for few additional seconds
supports activities that require short bursts of intense muscle
Nutrients in aerobic respiration
glucose, glycogen, fatty acids
breakdown within fibers provide ATP required to support continued activity
Aerobic Metabolism (respiration)
Long Term Energy
occurs if sufficient O2 available to muscle
produces ATP by breaking down glycogen, glucose, and/or fatty acids
A LOT OF INCREASE ATP but is slow and requires oxygen
supports primarily light to moderate exercise
role of exercise in aerobic metabolism
exercise leads to an increase in breathing rate and depth and an increase in blood flow to skeletal muscle which also leads to increase oxygen delivery
pros and cons of aerobic metabolism
pros: increase in ATP
cons: slow
anaerobic metabolism (respiration)
short term energy
breaks down glycogen and glucose into lactic acid (non-O2 utilizing)
occurs during periods of intense muscular activity when O2 cannot be supplied fast enough
faster…can produce more ATP than aerobic metabolism over a limited time
uses increased glucose
generates H+
pros and cons of anaerobic metabolism
pros: no oxygen needed, fast
cons: less ATP, generates acid
Muscle fatigue
inability of a muscle to maintain a particular strength of contraction overtime
What might cause muscle fatigue
may be due to decreased nutrients, decrease calcium release from SR, and increased H+ (muscle acidity)
note - psychological fatigue or central fatigue is different = feeling tired occurs before muscle fatigue
oxygen debt
difference between the resting rate of O2 consumption and the increase rate following exercise = recovering oxygen uptake
contractile elements
those muscle structures actively involved in contraction (ex. thick and thin filaments)
series elastic elements
structures that resist stretching (but can be stretched)
located between the contractile elements and load including CT (ex. tendon)
internal tension
the force generated by the contractile elements
external tension
force exerted on load
Tension
force exerted by contracting muscle on an object (opposite from load)
isotonic contraction
constant tension in muscle while length changes (ex. when muscle is moving a load)
concentric isotonic contraction
muscle shortens
eccentric isotonic contraction
muscle lengthens
isometric contraction
muscle develops tension, but no length change
example - when maintaining posture OR attempting to move a load that is greater than the tension developed
twitch contraction
the mechanical response of a muscle fiber or motor unit to a single AP
muscle contracts rapidly, then relaxes
last longer than AP
3 phases (latent, contraction, relaxation)
Latent period
delay immediately following stimulus arrival; short (a few msecs); associated with excitation - contraction coupling processes
contraction period
tension develops, cross bridges form