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aeldavies
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Functions of Skeletal Muscle
- Produce movement
- Maintain body posture/position
- Support soft tissues
- Guard entrances and exits
- Maintain body teperature
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Types of Movement
- Concentric and eccentric isotonic contractions
- Flexion
- extension
- abduction (towards body)
- addutction (away from body)
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Isometric contractions
helps maintain body posture and body position
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Maintaining body temperature
- Shivering (warm up)
- Vasodilation (cool down)
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5 levels of muscle organization (large to small)
- body
- fascicles
- fibers
- myofibrils
- sacromeres
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myofibrils
- made from sacromeres in series
- from 2 proteins
- myosin and actin
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contraction
- sliding of myosin and actin
- z lines move closer
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myosin (thick filament)
- made of proteins
- looks like 2 golf clubs twisted together
- actin binding site
- ATP site
- hinge
- High engery (big angle)
- Low engery (small angle)
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Actin (thin filament)
- looks like 2 strands of pearls twisted together
- Tropomyosin (thread-like protein)
- Troponin (found in intervals)
- G-actin (myosin binding sites)
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how Ca++ regulates binding sites on actin
Ca++ released from sarcoplasmic reticulum
Ca++ binds to troponin complex
Tropomyosin moves off the myosin binding sites of the actin filament
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Resting states of Actin
Myosin binding sites are covered by tropomyosin
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Muscle about to contract
- Binding site of actin is exposed due to Ca++ released from S.R. and shifting tropomyosin off
- g actin
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10 steps in mechanism of muscle contraction
- 1. Ca++ released from S.R., binds to troponin, causes active sites on actin to be exposed
- 2. ATP binds to myosin head
- 3. ATP hydrolyzed to ADP and Pi (still bound by myosin)
- 4. Myosin head goes into high energy state ("cocked")
- 5. Myosin head attaches to active site of actin molecule
- 6. Pi is released from myosin head
- 7. Myosin head goes to low energy state, producing "power stroke"
- 8. Myosin and actin in rigor state and ADP is released from myosin head
- 9. New ATP binds to myosin head and detaches from actin filament (rigor state ends)
- 10. Repeats from #2
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Entire mechanism of muscle fiber contraction
- 1. Action potential down motor neuron
- 2. Acetylcholine (ACh) is released by neuron
- 3. ACh binds to nicotinic receptors Na+ influx & K+ efflux (net depolarization of cell)
- 4. New action potential propagates along muscle fiber
- 5. Action potential enters fiber via transverse tubules
- 6. Ca++ channels open in S.R. releasing Ca++ into cytosol
- 7. Ca++ binds to troponin, causing tropomyosin to slide off active sites on actin filaments
- 8. Molecular mechanism of actin and myosin movement occurs
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Muscle Mechanics: The Twitch
- 1. Latent phase
- 2. Contraction phase
- 3. Relaxation phase
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Latent phase in muscle twitch
- 1. action potential travels along muscle fiber and into the t-tubules
- 2. Ca++ channels in SR open
- 3. Ca++ floods into cytosol
- 4. Ca++ binds to troponin
- 5. Tropomyosin moves off of myosin binding sites on actin
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Contraction phase of twitch
- 1. Myosin head attach to the actin and do the "power stroke"
- 2. Myosin heads bind a new ATP, release from the actin, recock, reattach, and perform another "power stroke"
- 3. Repeats a few times
Increase in tension, depending on muscle fiber can last 50 ms
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Relaxation phase in muscle twitch
- 1. Ca++ is pumpled back into SR
- 2. tropomyosin covers up the myosin binding sites on actin
- 3. myosin is no longer able to bind to actin
Decreases in tension and depending on muscle fiber can last 50 ms
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Fused (complete) tetanus
Can't see where action potentials are because they are so close together
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Twitch summation
you can see on the graph where a bump is, is where and action potential has occured
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Unfused tetanus
a sustain contraction, action potentials keep occuring and keep seeing bumps as tension increases
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Isotonic contraction
- Lifting weights (same tension)
- 1. straining (concentric)
- 2. Tension (plateau)
- 3. Shortening length (eccentric)
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Isometric Contractions
- Strain against load
- muscle fibers never shorten
- Never enough tension to lift load
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True or False: Does an isotonic contraction progress to am isometric contraction as the load placed upon the muscle increases?
TRUE
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Motor Units
A group of muscle fibers that are all controlled by the same motor neuron.
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Motor units vary in size
- Extraocular muscles (fine dexterity)
- few muscle fibers per motor unit
- Gastrocnemius (leg)
- thousands of muscle fibers per motor unit
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What is motor unit recruitment?
the turning on of more then one motor unit to complete an action
small motor units recruit first then larger ones
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What is motor unit rotation?
the switching or changing of motor units to prevent muscle fatique
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"Size Principle" of motor unit recruitment
Use small first the progressively larger are recruited.
Motor neurons that control certain muscles are controlled by interneurons in CNS
Interneurons begin to fire, and motor neurons with smaller cell bodies will reach -55 mV (threshold) before (few EPSPs) motor neurons with larger (more EPSPs) cell bodies
small motor units are innervated by smaller neurons with smaller cell bodies, thus fire first in sequence
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Load and shortening velocity for skeletal muscles
the more load we put on muscles the shorter the shortening velocity
remember velocity is the change in distance over the change in time
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3 Engery sources for muscle contraction
- 1. phosphagen system
- 2. Glycogen-lactate system (anaerobic)
- 3. Aerobic system
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Phosphagen system
- ATP & phosphocreatine (PC)
- creatine-PO4 + ADP -> Creatine + ATP
Rate of energy release: 4 moles of ATP per min
Size about 10 s (3 s of ATP and 6 s of PC)
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Glycogen-lactate system (anaerobic sytem)
Glycolysis & fermentation
sugar -> pyruvate -> lactate
Rate of energyy release: 2.5 moles
Size about 90 s
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Aerobic system
Doing all the steps of cellular respiration
Glycolysis, pyruvate decarboxylation, citric acid cycle, and the electron transport chain
O2 + Sugar -> CO2 + Water
Rate of energy release: 1 mole of ATP/min
unlimited duration, as long as nutrients last
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Classification of muscle fibers
Type 1 (slow-oxidative)
Type 2a (fast-oxidative)
Type 2x (fast-glycolytic)
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Oxidative
likes using oxygen and aerobic reserviors
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Type 1 (Slow-oxidative)
- Slow myosin ATPase
- Slow contraction
- Longer time to fatique
- High use oxygen
- Low use glycolysis
- Many mitochondria
- Many capillaries
- Lots of myoglobin
- Red color
- Low glycogen content
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Type 2a (fast-oxidative)
- Fast myosin ATPase
- Fast contraction
- intermediate time to fatigue
- high oxygen use
- intermediate glycolysis
- many mitochondria
- many capillaries
- alot of myoglobin
- red in color
- intermediate glycogin content
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Type 2x (fast-glycolytic)
- Fast myosin ATPase
- fast contraction
- short time to fatique
- low oxygen use
- high glycolysis use
- few mitochondria
- few capillaries
- less myoglobin
- white in color
- high glycogen
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Muscle fatique
- Oxidative fibers
- glycogen depletion and increased temperature
- Fatigue of glycolytic fibers
- Possible accumulation of lactate, mechanical injury to muscle fiber, lack of blood supply and increased temperature
- True neuromuscular fatique
- depletion of ACh from motor neuron termini, and only occurs in artificially stimulated neurons and muscle fibers.
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Torque
Produced by a load around a joint is equal to the torque produced by the muscle around the same joint.
Is equal to the force on a lever multiplied by the length of the lever arm.
T = ( r X F)
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True or False: Skeletal muscles have a mechanical advantage because they can produce a force less then the actual force that gravity is directly producing on the load.
FALSE, skeletal muscles have a mechanical distadvantage and must produce a force in excess of the actual force that gravity is directly producing on the load.
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Mechanical disadvantage of bones and muscles as levers and forces
The mechanical disadvantage permits a small (and slow) shortening of the muscle to result in the long (and fast) movement of a load.
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Where is smooth muscle found?
- (Autonomic Nervous System)
- digestive tract
- blood vessels
- bronchioles of lungs
- eye (iris and ciliary body)
- reproductive and urinary tract
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Smooth Muscle
- Found in hollow organs and tubes
- a cell has a single nucleus
- shorter than skeletal muscles
- develops tension slowly and relaxes slowly, resulting in longer contractile response (twitch)
- Not striated (actin/myosin not arranged)
- actin filaments radiate out of "dense bodies"
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Contraction of smooth muscle
- regulated by Ca++
- No troponin
- instead uses calmodulin to control muscle contraction (movement is not predictable)
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Signal Transduction for Smooth Muscle Contraction
- 1. Ca++ enters cytosol from extracellular fluid and from SR
- 2. Ca++ binds to calmodulin in cytosol
- 3. Ca-calmodulin activates myosin light chain kinase
- 4. Myosin heads are activated (phosphorylated) by MLCK
- 5. Phosphorylated myosin attaches to actin filaments and completes the "power stroke"
Takes time to turn on/off because of enzymes
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