physio exam 3

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165 Terms

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functions of controlled muscle contractions
* purposeful movement of the whole body or parts of the body
* manipulation of external objects
* propulsion of contents through carious hollow internal organs
* emptying of contents of certain organs to external environment
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skeletal muscle
striated, voluntary, multi nucleated

attached to bones of skeleton (movement of body in relation to external environment)
striated, voluntary, multi nucleated 

attached to bones of skeleton (movement of body in relation to external environment)
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cardiac muscle
striated, involuntary, intercalated disc

wall of heart (pumping blood out)
striated, involuntary, intercalated disc

wall of heart (pumping blood out)
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smooth muscle
unstriated, involuntary, spindle-shaped

walls of hallow organs (movement of contents with hollow organs)
unstriated, involuntary, spindle-shaped

walls of hallow organs (movement of contents with hollow organs)
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mesenchymal cells
multipotent stem cells

important for making and repairing skeletal muscles
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myoblasts
embryonic precursor of myocytes
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myotube
developmental stage of a muscle fiber composted of a syncytium formed by fusion of myoblasts
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myocyte
unit of muscle tissue that contains bundles of myofibrils
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myofibril
contain sarcomeres connected in a series

1 um in diameter, make up 80% of the muscle fiber
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sarcomere
the smallest functional (contractile) unit of skeletal muscle fiber and is a highly organized arrangement of contractile, regulatory, and structural proteins
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muscle fiber
long, cylindrical, 10-100um in diameter and 750,000 um (2.5 ft in length)
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thick filaments
special assemblies of the protein myosin
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thin filaments
smaller filament size and made up of the protein actin
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A band
dark, stacked set of thick filaments

thin filaments overlap in this region
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H zone
the lighter region of the A band, this region does not contain the filament oveerlap
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M line
support proteins that hold the thick filaments together vertically
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I band
contain thin filaments that do not go into the A band
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Z line
a dense vertical cytoskeletal disc that defines the boundaries of the sarcomere. anchors thin and titin filaments
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titin
highly elastic protein. providing parallel stability, elasticity, and signal transduction
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scaffold
sarcomere stability

along with M line proteins (vertical stability), titin helps stabilize the position of thick filaments in relation to thin filaments (parallel stability)
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elastic spring
titin acts as a recoil spring

when a muscle is stretched, titin helps the muscle recoil back to its rest position
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Signal Transduction
titin is involved in the muscle enlargement pathway in response to weight lifting
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myosin
protein consisting of two identical golf club-like subunits (intertwined tails, two globular heads, two hinges)
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forming cross-bridges
the heads contains an actin binding site and a myosin ATP site
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actin
primary structural component

spherical in shape, they contain binding sites for the myosin

they are arranged in two twisted strands (actin helix)
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tropomyosin
thread-like proteins that lie end to end on the actin helix, covering the actin sites at rest
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troponin
a complex made of three polypeptide units, binding to: tropomyosin, actin, and Ca2+
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Relaxed

1. no excitation
2. no cross-bridge binding because cross-bridge binding site on actin is physically covered by troponin-tropomyosin complex
3. muscle fiber is relaxed
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excited

2. muscle fiber is excited and Ca2+ is released
3. released Ca2+ binds with troponin, pulling troponin-tropomyosin complex aside to expose cross-bridge binding site
4. cross-bridge binding occurs
5. binding of actin and myosin cross bridge triggers power stroke that pulls thin filament inward during contraction
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Power Stroke Steps

1. binding
2. power stroke
3. detachment
4. binding
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SERCA Pump
* actively transport Ca2+ from cytosol to lateral sacs
* this allows the troponin-tropomyosin complex slip back into its blocking position
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latent period
excitation-contraction coupling must occur before cross-bridge activityc
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contraction time
time from contraction onset to peak tension (15-50ms) this cannot end until the Ca2+ has been removed
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Relaxation time
time from peak tension to relaxation (15-50ms)
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skeletal muscle biomechanics
applying physics to study mechanical principles of biological systems. transforming chemical energy to mechanical energyt
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tendon
tough, elastic, connective tissue that connects whole muscle groups to bones
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muscle tension
the tension produced in the muscle that is applied on bones via tendon
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contractile component
when the sarcomeres shorted, due to cross-bridge cycling, this tension is only within the muscle itself
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series-elastic component
refers to the elastic, non-contractile tendons

shortening of the sarcomeres stretches the series-elastic component, transferring muscle tension to the bone
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origin
the muscle attached to the more stationary bone
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insertion
muscle attached to the bone that is moving
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isotionic
constant tension
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concentric isotonic
if the force the muscle produces is greater than the opposing force, the muscle shortens
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eccentric isotonic
if the force the muscle produces is less than the opposing force, the muscle lengthens
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isometric
constant length
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isokinetic
constant velocity
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work
force multiplied by distance
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force
the muscle tension required to overcome the load (weight of the object)
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fulcrum
elbow joint
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power arm
distance between fulcrum and the insertion
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load arm
entire arm from fulcrum to hand
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lever ration
power arm : load arm
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distance and velocity
muscle shortening / lever ratio
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force
weight of object / lever ration
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no summation
if a muscle fiber is restimulated after it has completely relaxed, the second twitch is the same magnitude as the first twitch
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twitch summation
if a muscle fiber is restimulated before it has completely relaxed, the second twitch is added on to the first twitch
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tetanus
if a muscle fiber is stimulated so rapidly that it does not have an opportunity to relax at all between stimuli, a maximal sustained contrtraction
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somatic reflex responses
no conscious effort, automatic
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volunatry movements
goal-directed movements initiated and terminated at will
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rhythmic movements
patterned movements
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central pattern generators
biological neural circuits that autonomously bring about patterned movements
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ATP production

1. creatine phosphate
2. oxidative phosphorylation
3. glycolysis
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creatine phosphate
* first energy source tapped at the onset of muscle contractions
* has a high-energy phosphate group that can be donated to ADP to form ATP and creatine
* reversible reaction
* pools in your muscles
* short bursts of high intensity can deplete the pools in 5-10 seconds
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creatine supplement
* side effects: high blood pressure, dehydration, upset stomach, muscle cramps
* make mania worse in bipolar disorder
* make kidney disease worse
* associated with a faster rate of parkinson’s progression
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glycogen
glucose is delivered to the muscles via the blood and is stored as chains of glucose

live stores excess
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oxidative phosphorylation
* utilizes glycogen and oxygen
* many enzymatic steps
* aerobic activity
* light exercise - walking, light jog, playing in the pool
* \
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mechanisms to increase O2

1. increase breathing
2. increase o2 storage/diffusion
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hemoglobin
4 globulins each with a hemes and iron

a1 a2 b2 b1
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myoglobin
able to bind and release o2 depending on o2 concentration and increases oxygen diffusion (whales have more of this)
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limitations to o2 delivery
lungs can only take in so much O2 and blood can only deliver so much

near maximal contractions also close blood vessels, limiting O2 supply
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glycolysis
occurs in absence of oxygen

its faster
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muscle fatigue
occurs when an exercising muscle can no longer respond to stimulation with the same degree of contractile active

it’s a defense mechanism to prevent the total loss of ATP
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cause of muscle fatigue
unclear but:

* could be due to a local increase in inorganic phosphate
* SERCA Ca2+ pump leakage - protease activation
* depleted glycogen stores
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central fatigue
when the CNS no longer activates the motor neurons supplying the muscle

poorly understood
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filaments in smooth muscle

1. thick myosin
2. thin actin
3. intermediate filaments
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intermediate filaments
binds to dense bodies to provide structural support for actin and myosin in smooth muscle
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smooth muscle thin filament
no troponin

tropomyosin is not covering the myosin binding site on the actin
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smooth muscle contraction
regulated by ANS through varicosities
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single unit smooth muscle
fibers connect as one through a syncytium via gap junctions

ex: visceral muscle
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multi unit
fibers act independently of each other

pupillary muscles
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pacemaker potentials
spontaneous potentials that always reach threshold

depolarization is induced by Ca2+ (not Na2+) and use L-type voltage-fated Ca2+ channels

repolarization L-type voltage-gated K+ channels
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slow wave potentials
constant depolarizations and repolarizations that do not necessarily reach threshold

largely unknown how this occurs
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stress-relaxation response
enables smooth muscle to exist in a variety of lengths with little change in tension
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circulatory system
the bodies system of transport
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heart
establishes a pressure gradient
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blood vessels
passageways for transport
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blood
transport medium
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pulmonary circulation
heart to lungs
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systemic circulaton
heart to body systems
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heart
hollow organ about the size of a fist

lies left in the thoracic cavity
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right side of heart
deoxygenated

serves pulmonary circuit
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left side of heart
serves systemic circuit

oxygenated
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superior/inferior vena cava
right side vessels leading blood to the atria
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pulmonary veins
left side vessels leading blood to the atria
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pulmonary trunk
right side vessels leading blood away from ventricles
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aorta
left side vessel leading blood away from ventricles
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pressure
the force on the vessel walls from the heart pumping the blood into themr
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resistance
friction between the blood and the vessel wall
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chordae tendineae
tendinous tissue connecting the valve to the papillary muscle
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papillary muscle
nipple

contracts with a ventricle contraction