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skeletal muscle tissues are composed of..
Skeletal muscle tissue
Nervous tissue
Blood
Connective tissues
connective tissue of skeletal muscle
Fascia: Thin covering of connective tissue around a muscle
Tendon: Cord-like mass of connective tissue that connects muscle to a bone
Aponeurosis: Sheet-like mass of connective tissue that connects a muscle to bone, skin, or another muscle
compartment syndrome
Fluid accumulation within a compartment
Results in increase in pressure in compartment
Leads to deficiency of oxygen and nutrients
Causes severe pain
thick vs thin filaments
a) Composed of myosin protein, heads form cross-bridges with thin filaments (creates chain of binding that allows ATPase enzyme in heads myosin to convert to energy for muscle contraction)
b) Composed of actin protein, associated with troponin and tropomyosin, which prevent cross-bridge formation when muscle is not contracting
neuromuscular junction
synapse where axon of motor neuron and skeletal muscle fiber interact to contract skeletal muscle fibers
parts:
Motor neuron: Neuron that controls skeletal muscle fiber
Motor end plate: Specialized folded portion of skeletal muscle fiber sarcolemma
Synaptic cleft: Space between neuron and muscle fiber, across which neurotransmitter travels
Synaptic vesicles: Membrane-bound sacs containing neurotransmitters
Neurotransmitters: Chemicals released by motor neuron to deliver message to muscle fiber
Acetylcholine
neurotransmitter that provides stimulus for muscle contraction
Nerve impulse causes release of ACh from synaptic vesicles
ACh binds to ACh receptors on motor end plate
ACh causes changes in membrane permeability to sodium and potassium ions, which generates a muscle impulse (action potential)
Impulse causes release of calcium ions from SR, which leads to muscle contraction
excitation-contraction coupling
muscle relaxation - Ca+2 ions are stored in SR, Troponin-tropomyosin complexes cover binding sites on actin filaments
muscle stimulation - Muscle impulses cause SR to release +2 Ca ions into cytosol, ion binds to troponin to change its shape, tropomyosin is held in place by a troponin molecule; change in shape of troponin alters the position of tropomyosin → binding sites on actin are now exposed
Myosin heads bind to actin, forming cross-bridges
sliding filament model of muscle contraction
When sarcomeres shorten, thick and thin filaments slide past each other
H zones and I bands narrow, Z lines move closer together, Thin and thick filaments do not change length
Overlap between filaments increases
cross bridge cycling
Myosin head attaches to actin binding site, forming crossbridge
Myosin cross-bridge pulls thin filament toward center of sarcomere
ADP and phosphate are released from myosin
New ATP binds to myosin
Linkage between actin and myosin cross-bridge break and ATP splits
Myosin cross-bridge goes back to original position, ready to bind to another binding site on actin
muscle relaxation
Acetylcholinesterase (enzyme) rapidly decomposes ACh remaining in the synapse (Muscle impulse stops when ACh is decomposed)
Stimulus to sarcolemma and muscle fiber membrane ceases.
Calcium pump moves +2 Ca back into sarcoplasmic reticulum (SR).
Troponin-tropomyosin complex again covers binding sites on actin.
Myosin and actin binding are now prevented (Muscle fiber relaxes)
energy sources for muscle contraction
`1. ATP reserves - first source of energy for muscle contraction
Creatine phosphate - Initial source of energy to regenerate ATP from ADP and P, Stores energy in phosphate bond, like ATP
cellular respiration - Must be used to fuel longer periods of muscle contraction, breaks down glucose to produce ATP, glucose stored as glycogen in muscle cells
myoglobin
stores extra oxygen in muscles carried from lungs by hemoglobin, increases the amount of oxygen available to support aerobic respiration
anaerobic (lactic acid) threshold
shift in metabolism from aerobic to anaerobic during strenuous muscle activity when the above systems cannot supply the necessary O2 → produces lactic acid
oxygen debt
At end of strenuous exercise, muscles may be left with oxygen debt
amount of oxygen needed by liver cells to convert the lactic acid to glucose, and to restore muscle ATP and creatine phosphate concentrations (stabilize metabolic activity)
muscle fatigue
inability to contract muscle
caused by: decreased blood flow, ion imbalances across sarcolema, loss of desire to continue the exercise, accumulation of lactic acid
muscle cramp
Sustained, involuntary muscle contraction
May be caused by changes in electrolyte concentration in extracellular fluids in the area
threshold stimulus
Minimum strength of stimulation of a muscle fiber required to cause contraction
action potential is generated when strength of stimulus reaches threshold
post threshold reached:
impulse spreads through muscle fiber, releasing +2Ca from SR and activating cross-bridge formation
One action potential from a motor neuron releases enough ACh to produce threshold stimulus in muscle fiber, causing a muscle impulse
twitch
Contractile response of a single muscle fiber to a single impulse
Periods of time associated with a twitch:
Latent period: Delay between stimulation and start of contraction
Period of contraction: Fiber pulls at attachments
Period of relaxation: Pulling force decreases
length - tension relationship
length of muscle fiber before stimulation determines amount of force it can develop
depends of number of cross bridges able to be formed which depends on optimal overlap
Optimum starting length is resting length of the muscle fiber; this allows the greatest force to develop
Stretched muscle fibers develop less force, since some myosin heads cannot reach binding sites on actin (too little overlap)
Shortened muscle fibers also develop less force, since compressed sarcomeres cannot shorten further (too much overlap)
summation
Process by which the force of individual muscle fiber twitches combine, when frequency of stimulation increases
Produces sustained contractions (partial tetany of tetany)
tetanus (partial vs complete)
partial - Occurs at higher frequencies of stimulation, time spent in relaxation between twitches becomes very brief
complete tetany - Occurs at very high frequencies of stimulation, only in laboratory, forceful sustained contraction has no relaxation between twitches
motor unit
motor neuron plus all the muscle fibers it controls
whole muscle has many motor units
coarse movements - produced with large number of fibers in a unit
precise movements - produced with fewer muscle fibers in a motor unit
recruitment
increase in the number of motor units activated to produce more force
smaller diameter axons recruited first and larger diameter axons when intensity of the stimulus increases bc they can produce sustained contractions of increasing strength
recruitment continues as intensity increases until all units activated
______ and ______ can produce sustained interactions of increasing strength
summation and recruitment
_____ muscle contractions are smooth movements
whole
muscle tone
continuous state of partial contraction in resting muscles; normal tension/firmness
maintains body posture
increases metabolic energy used
isotonic contraction
Muscle contracts and changes length
Concentric: when muscle tension is greater than load, muscle shortens
Eccentric: when muscle tension is less than load, muscle lengthens
isometric contraction
muscle contracts but does not change length, and tension develops but parts attached to muscle do not move
slow twitch fibers (type I)
Always oxidative
Resistant to fatigue
Red fibers (Abundant myoglobin)
Good blood supply
Many mitochondria
Slow ATPase activity; slow to contract
fast twitch fatigue resistant fibers (type IIa)
Intermediate twitch fibers
Intermediate oxidative capacity
Intermediate amount of myoglobin
White fibers
Resistant to fatigue
Rapid ATPase activity
fast twitch glycolytic fibers (type IIb)
Anaerobic respiration (glycolysis)
White fibers (less myoglobin)
Poorer blood supply than slow-twitch fibers
Fewer mitochondria than slow-twitch
More SR than slow-twitch
Susceptible to fatigue
Fast ATPase activity; contract rapidly
smooth muscle fibers
Shorter
Single, centrally located nucleus
Elongated with tapering ends
Myofilaments randomly organized
Lack striations
Lack transverse tubules
Sarcoplasmic reticulum (SR) not well developed
multi unit smooth muscle vs visceral smooth muscle
A) Cells are less organized, Function as separate units, Fibers function independently, Iris of eye, walls of blood vessels, Stimulated by neurons/hormones
B) Single-unit smooth muscle; cells respond as a unit, Sheets of spindle-shaped muscle fibers, Fibers held together by gap junctions, Exhibit rhythmicity, Conduct peristalsis, Walls of most hollow organs, More common type of smooth muscle
smooth muscle characteristics
location: blood vessels, reproductive system, glandular system, digestive, urinary and intergumentary system
Description: non-striated, no sliding filaments, single central nucleus, loose arrangement of filaments,
Filaments structure: myosin fibers have more heads per filament, thin filaments attached to dense bodies
cellular characteristics: free calcium ions in cytoplasm triggers contraction
How does ATP function in skeletal muscles?
muscles store enough ATP to start the contraction and manufacture more as needed
ATP - active energy
creatine phosphate - NRG storage in resting muscle
creatine phosphokinase - enzyme that regens ADP to ATP
Layers of connective tissue of skeletal muscle
Epimysium
D: collagen later connected to the deep fascia
F: separates the muscles from surrounding tissue
Perimyseum
D: surrounds muscle fiber bundles (fascicles)
F: contains blood vessels and nerve supply to vessicles
Endomysium
D: surrounds muscle fiber cells (fibers)
F: contains capillaries and nerve fivers contacting muscle fibers and myosattelite cells (stem cells) that repair damage
What cells do skeletal muscles develop from?
Mesodermal cells (myoblasts)
function of sarcomeres
transmission of action potential for muscle contraction
actin vs myosin
a) twisted strands of globular molecules with myosin binding site
b) has head and tail; tail- binds to other myosin molecules and head -2 globular protein that reaches the nearest thin filament (form cross bridge with actin by a pivoting motion
tropomyosin and troponin
a) double strands that cover 7 active sites on actin, binds to troponin
b) protein w 3 binding subunits (subunit binding to tropomyosin, subunit binding to actin to hold complex in place, subunit with receptor that binds to Ca2+ ions)
Excitation contraction coupling
action potential arrives at neuromuscular junction
neurotransmitter acetocholine released at terminal and binds to receptors on sarcolemma
acetocholine at receptor causes change in membrane permeability allowing sodium to enter from outside the cell
action potential created in the sarcolemma due to depolarization as positively charged sodium ions make membrane less negatively charged
depolarization causes waves through tubule that lead to the release of calcium ions from the sarcoplasmic reticulum
action potential traveling through T tubule causes release of calcium from the sarcoplasmic reticulum
calcium ions bind to receptors on troponin which react by changing shape and moving away from tropmyosin (complex broken)
Actin can now bind to myosin initiating sliding filaments
relaxation - signal from nervous system makes acetylcholine disappear and remaining are reabsorbed by neuron or broken down by enzymes
repolarization - causes calcium to come off troponin receptors and be reabsorbed
troponin goes back to OG shape covering binding sites
frequency of stimulation
how many successive twitches reach a muscle fiber
treppe
stair step increase in twitch tension that is caused by repeated stimulations immediately after relaxation phase
wave summation
increasing tension of summation twitches (tension builds more rapidly and relaxation phase overlaps with twitch cycle)
maximum tension
all motor units reach tetanus, only can be sustained for a very short time
sustained tension
less than maximum tension allows for rest periods and facilitates smoother movement
aerobic metabolism
prinmary NRG source of resting molecules (breaks down fatty acids to produce 34 ATP per glucose)
anaerobic glycolysis
primary NRG source for peak muscular activity, produces 2 moles ATP per one mole glucose (stored as glycogen in the skeletal muscles)
lactic acid is byproduct of this
lack oxygen to support mitochondria
recovery period
time taken for muscles to return back to normal
oxygen becomes more available
mitochondrial acitvity resumes
cori cycle
removal and recycling of lactic acid in the liver to produce pyruvic acid which becomes energy
muscle metabolism
muscles at rest - metabolise fatty acids and store glycogen
light activity - generate ATP through the breakdown of carbs lipids and amino acids
peak activity - NRG provided by anaerobic reactions
horomones influence
power vs endurance
a) max tension that muscle can produce
b) max time an activity can be sustained
both depend on types of fibers and conditioning
types of muscle fibers
fast fibers - contract quickly, large glycogen reserves, few mitochondria (for coarse mvmnt)
slow fibers - slow to contract and fatigue, sm diameter, more mitochondria, contain myoglobin (pigment that binds oxygen)
intermediate fibers - mid sized, low myoglobin, more capillaries, slow to fatigue
muscle hypertrophy vs muscle atrophy
a) muscle growth from heavy training increases diameter of fibers, mitochondrial acitvation, glycogen reserves
b) lack of activity reduces tone/size/power, and prolonged inactivity may result in muscle being replaced with fibrous muscle
cardiocytes
small, 1 nucleus, striated, short wide tubules, aerobic, intercalated discs for communication
intercalated discs
specialized intercellular junctions that join cell membranes of adjacent cardiocytes via gap junction or desmosome
functions: maintain structure, enhance molecular/electrical connections, conduct action potentials
characteristics of cardiac tissue
automaticity - contraction w/o stimulation (controlled by pacemaker cells)
variable contraction tension - influenced by nervous system
extended contraction time
prevention of wave summation and tetanic contractions by cell membranes
types of smooth muscle
multi unit smooth muscle - D: Cells are less organized, Function as separate units stimulated by neurons and horomones, fibers function independently L: Iris of eye, walls of blood vessels
visceral smooth muscle - D: Single-unit smooth muscle; cells respond as a unit, Sheets of spindle-shaped muscle fibers, Fibers held together by gap junctions, Exhibit rhythmicity • Conduct peristalsis L: Walls of most hollow organ, More common type of smooth muscle
smooth muscle contraction
calmodium instead of troponin •
Two neurotransmitters affect smooth muscle: Acetylcholine (Ach) and norepinephrine (NE)
Hormones can stimulate or inhibit smooth muscle
Stretching can trigger smooth muscle contraction
slower to contract and relax
more resistant to fatigue
can change length without changing tautness
agonist
muscle that causes an action
includes prime movers - Agonist primarily responsible for movement
e.g. bicep is agonist (flexion) and antagonist is triceps (extension)
synergist
Muscles that assist agonist/prime mover
antagonist
Muscles whose contraction causes movement in the opposite direction of the prime mover
parallel muscles
fibers parallel to the long axis of the muscle
Ex. biceps brachii - fibers run paralell in vessicle arrangement
convergent muscles
a broad area converges on an attachment site that pull in different directions that include tendons, apneurosis, or raphe (groove of connective tissue)
e.g. pectoralis muscle
Pennate muscles
form an angle with the tendon
do not have as large range of motion as parallel muscles
contain more myofibrils than parallel muscles
develop more tension
types
unipennate - fibers on one side of the tendon (e.g. extensor digitorum)
bipennate - fibers on both sides of the tendon (e.g. rectus femorus)
multipennate - tendon branches within the muscle, more complex (e.g. deltoid muscle)
circular (sphincters)
open and close to guard the entrances to the body
e.g. orbicularis oris and muscles around eyes
Lever
bones are rigid moving structure with a fulcrum (fixed point aka joint)
first class lever
seesaw like structure with central fulcrim applied between force and load
e.g. sternocleidomastoids - weight that must be overcome is weight of head and fulcrum is C1 and joint
second class levers
wheelbarrow; center load between applied force and fulcrum
small force moves large weight
e.g. gastricnemeus and soleus muscles raising the leg
third class levers
most common in the body, center applied forced between load and fulcrum and greater force moves smaller load
greater force maximizes speed and distance traveled
e.g. biceps brachii and shoulder joint
origin and insertion
origin: fixed point
insertion: moving point
most muscles originate or insert on the skeleton
origin is usually proximal to insertion
axial muscles vs appendicular muscles
a) position head and spinal collumn, move rib cage (60% skeletal muscles)
b) support pectoral and pelvic girdles, limbs (40%)
orbicularis oris
constricts the mouth opening
buccinator
muscle responsible for moving food around the cheeks
masseter
strongest jaw muscle
rotator cuff muscles
SITS - frequently injured
supraspinatous
infraspinatous
teres minor
subscapularis
and tendons
muscles that move the forearm and the hand
originate on humerus and insert on forearm
extensors - mainly on posterior and lateral surfaces of the arm
flexors - mainly on the anterior and medial surfaces
fixator
a muscle that acts to stabilize the origin and other parts of the body effective for movement
sternocleidomastoid
rotates the head
membrane voltage is generated by..
first by the movement of sodium ions (Na+) into the cell, and later the movement of potassium ions (K+) out of the cell through specified protein channels in the plasma membrane (referred to in muscle cells as the sarcolemma)
power stroke
movement of myosin when binding to actin
summation
excitatory postsynaptic potentials and inhibitory possynaptic potentials are added together at trigger zone → combined voltage determines yes or no action potential
vessicle trafficking
membrane recycling'; synaptic vessicle becomes part of cell membrane as it releases neurotransmitter → endocytosis returns membrane tp cytoplasm and forms new vessicles
neuropeptides
act as neurotransmitters or neuromodulators (substances which alter a neurons response to a neurotransmitter or block relase)
e.g. ekephalins - relieve pain sensations
neuronal pools
groups of interneurons taht connect with each other and are located in CNS (cell bodies may be located in different parts) → work together to perform a common function
each recieves input and generates output to/from other neurons
may affecr other pools/peripheral effectors
faciliatation
repeated impulses on an excitatory presynaptic neuron may cuase that neuron to release more neurotransmitters in response to a single impulse → increases likelihood of postsynaptic cell reaching threshold
convergence vs divergence
1 neuron recieves input from several neurons → allows for collecting, processing, responding, to info from diff types sensory receptors
1 neuron sends impulses to several neurons via branching of its axon → may activate several motor units in a skeletal muscle
multipolar neurons
99% of neurons with processes extending from cell body
bipolar neurons
1 dendrite to 1 axon; located in the eyes, ears, and nose sensory receptors
unipolar neurons
1 process from cell body and 2 branches that function as an axon
L: mainly in ganglia of PNS
sensory/afferent neurons
unipolar or bipolar
interneurons
link neurons in CNS to relay info from 1 pt CNS to another
motor neurons
multipolar neurons; in somatic control skeletal and in autonomic control smooth and cardiac glands
astrocyte
type neuroglia that connects neurons to blood vessels exchanaging nutrients and growth factors (neurons that stimulate cell division)
form scar tissue
aid metabolism in some substance
regulate ion concentration
part of makeup blood brain barrier
oligodendrocytes
type of neuroglia that myelinate CNS axons and provide structural support
ependymal cells
line central spinal cord and ventricles of brain, cover choroid plexuses (CSF secreting), help regulate composition CSF
ciliated cuboidal or columnar cells
microglia
phagocytes that provide structural support
neuroglia of the PNS
Shwann cells
sattelite cells - support ganglia by nourishing and balancing ionic concentrations
neurom regeneration of PNS
axon separated from body and myelin sheath degenerates
shwann cells and neurilemma (surrounds myelin sheath) remain
remaining shwann cells provide guiding sheath for growing axon
neuron regeneration of the CNS
regeneration unlikely because no neurilemme to act as guiding sheath and oligodendrocytes dont proliferate post injury