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89 Cards in this Set
- Front
- Back
what are the properties of white muscle
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easily fatigued
short duration high affinity for ATPase lack myoglobin |
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what are the properties of red muscle
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more resistant to fatigue
long duration red b/c of myoglobin and capillary vessels smaller than white muscle |
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what are the properties of intermediate muscle
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appear like white muscle but have more resistance to fatigue than white muscle
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what increases during hypertrophy
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creatine phosphate, ATP, glycogen, and size of muscle
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this is a decrease in muscle diameter
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atrophy
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what happens if muscle is inactive for more than a month
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it will undergo disuse atrophy and a 50% decrease in size
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what occurs if you dont use the muscle
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the body stops sending nutrients to it and it decreases in size
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what is denervation atrophy
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when the nerve supply to a muscle is cut off it results in decrease in muscle size Ach receptors will spread all over the muscle membrane and the muscle will lose its ability to regain muscle activity if not innervated in 3-4 months
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what happens after 3-4 months of deenervation
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muscle shortens and is replaced with connective tissue, muscle fibers start dying
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what are some of the tropic effects of muscle and nerve on each other
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nerve tells muscle whether it is fast or slow twitch
nerve dies if it doesnt innervate muscle innervation of embryonic muscle causes the multiple Ach receptors to disappear |
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what is fasciculation
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twitching of a group of muscle somewhere in the body at a constant rate
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what cause fasciculation
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when a motor neuron dies it spills out Ach which causes nearby muscle to twitch
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what is fibrilation
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random twitching, each muscle twitches on its own
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what causes fibrilation
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when muscle fibers haven't been enervated they become very sensitive to Ach in the vicinity
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waht does muscle contraction do to blood flow and ischemic pain
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contraction of muscle squezes out blood from blood vessels resulting in not enough O2
pain is due to accumulation of biproducts (lactic acid) that stimulate the pain receptors |
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what are the effects of aging on muscle
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muscle fibers become smaller in size due to lose of muscle fibrils
muscle become less elastic due to accumulation of connective tissue blood flow decreases decrease in efficiancy of cardiovascular system and endurance recovery from injury is slow because low number of satelite cells |
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what are the three types of cardiac muscle
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atrial ventricular
pacemaker excitatory-conductive |
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what are the contractile muscles of the heart
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atrial ventricular
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what do impulses of the heart go through
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excitatory-conductive tissue
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what are the properties of excitatory-conductive tissue
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weak contraction
can conduct electricity to other parts of the heart can discharge electric impulses rhythmically |
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what allows cardiac muscle to be functionally syncitial
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interlocated discs
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what happens when you stimulate one muscle in the cardiac muscle
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it stimulates all the other muscles as well
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what are the specialized ridges along the sides of the interlocatted discs
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gap junctions, tight junctions, desmosomes
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what is the electrical synapse of the heart
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interlocated discks
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what do gap junctions, tight junctions, and desmosomes do
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cytoplasmic ridges that allow ions to travel from one cell to another therefore allowing transmission of impulses from cell to cell
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what is the form of electrical transmission in the heart
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gap/tight juctions and desmosomes
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what are atrial and ventricular muscle similar to
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skeletal muscle
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why is cardiac muscle not independent
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due to interlocated discs
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what is the RMP of atrial ventricular muscle
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-85 to -90
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what is the RMP of pacemaker
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-50 to -60
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what is the RMP of excitatory-conductive tissue
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-90 to -100
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what are excitatory-conductive tissue
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modified muscle cells that behaves like nerve and they hardly contract
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how does the atrial AP compare to the ventricular AP
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the atrial AP has a shorter duration and no plateau
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what is another name for the pacemaker potential
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SA nodel potential
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what is involved in the upstroke in the pacemaker potential
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Ca
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in the PQRST wave what does
P stand for QRS stand for T stand for |
P - atrial contraction (depolarization)
QRS - ventricular (depolarization) T - ventricular relaxation |
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what is the difference between the sarcotubular system of cardiac muscle vs skeletal muscle
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small termianl cisternae
poorly devloped sarcoplasmic reticulum t-tubules 5x diameter of skeletal a lot more mitochondria than in skeletal |
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what is unique about the tubular system in cardiac muscle
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5x diameter of skeletal
contains mucopolysaccharide that has the ability to hold Calcium Release Ca is pumped back into the tubules and sarcoplasmic reticulum |
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when an AP is generated in the cardiac muscle where is calcium released
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from the t-tublues and terminal cisternae
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where is Ca released in skeletal muscle and cardiac muscle in order to cause a contraction
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sacromere
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what are the sources of Ca in cardiac muscle
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t-tubules (major)
mitochondria (minor) |
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what is the role of Ca
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Ca causes a contraction
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why can't cardiac muscle be tetanized
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due to its long refractory periods (300 of 350 msec is absolute)
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how does cardiac muscle obey the all or nothing rule
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either all of the cardiac muscles contract or none of them
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what is the mitochondrial functions relating to Ca
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mitochondria can release and store Ca
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what is a safety mechanism for cardiac muscle
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having long refractory periods which prevent it from being tetanized
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what does the fiber length-tension relationship (Frank Sterling law) deal with
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the longer cardiac muscle is stretched the greater the force of contraction until it reaches a certain length in which if stretched you have a decrease in force of contraction
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when does cardiac muscle stretch
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when it is filled with blood
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when does a decrease in cardiac muscle contraction occur
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congestive heart failure
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what is the ionotropic effect
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increase in the force of contraction of the heart
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what is the chronotropic effect
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increase in the rate of contraction
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what is dromotropic effect
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increase of speed of conduction of the response
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what increases the ionotropic effect
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epinephrine/norepinephrin
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what has a negative ionotropic effect
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congestive heart failure
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what has a positive ionotropic effect
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stretching of the muscle fibers
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what are the two types of innervation in the heart
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cholinergic and adrenergic
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what does cholinergic innervation do
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innervates the SA node and some of atrium
decreases rate of heart beat modulates heart rate |
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what does adrenergic innervation do
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innervates two ventricles
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what are the two types of smooth muscle
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unitary (visceral) and multiunit
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what are properties of unitary
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functional syncytial
have nexus (gap junctions) connecting each cell sparse innervation |
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what are properties of multiunit
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like skeletal muscle
each cell is surrounded by polysacharide membrane innervated individually and driven by nerve impulse exist in small parts of the body (iris) |
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what forms can smooth muscle exist in
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smooth muscle is very small
sheeths (parallel) spindles (tight or loose) |
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where are spindles found
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around tubular tissue
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what are the majority of AP in smooth muscle
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in unitary (visceral) smooth muscle they are spike
multiunit smooth muscles don't have an AP |
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in what cases does a plateau occur in smooth muscle
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in unitary (visceral) smooth muscle in the uterus during birth
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what is the RMP of smooth muscle
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-50 to -60
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how do AP in smooth muscle compare to skeletal
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smooth muscle AP are much longer than skeletal
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what happens if you stretch smooth muscle
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it will contract
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what does stretching do to smooth muscle
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it changes the permeability of ions
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waht does smooth muscle not have
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troponin, instead has an enzyme similar to it
has a rudimentary sarcotubular system no t-tubules have ridges call careoli instead no striation meaning no sacromere no endplates |
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instead of EPP what does smooth muscle have
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EJP and IJP
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how does the force of contraction in smooth muscle compare to skeletal
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the force of contractions is almost equal
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how is smooth muscle believed to contract
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sliding filament hypothesis
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what drives the AP in the heart
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SA node (pace maker)
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what is the organization of smooth muscle
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caveoli are t-tubules of smooth muscle
Sarcoplasmic Reticulum has no terminal cisternae a lot of cross bridges of myosin |
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what doesn't smooth muscle need t-tubules
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due to the small size of the smooth muscle meaning it is easy for Ca from outside to cause a contraction
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where does the Ca for a smooth muscle contraction come from
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outside of the cell
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what defines the latent period in smooth muscles
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the latent period is the time in which calcium channels open until a contraction occurs
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how does the latent period of smooth muscle compare to skeletal muscle
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the latent period is 50x longer due to how slow Ca channels open
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how does smooth muscle contraction compare to skeletal
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the contraction is longer due to how slow Ca is removed by the pump
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how does the energy requirements of smooth muscle compare to skeletal/cardiac
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smooth muscle requires 300x less energy
no troponin instead have calmodulin |
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what is the enzyme that smooth muscle uses in place of troponin
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calmodulin
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what is calmodulin and how does it work
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calmodulin is an enzyme that will bind to calcium forming the calmodulin calcium complex and it will phosphorylate the myosin light chain kinase which in turn primes the thick filaments (cross bridges) to interact with actin
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why does smooth muscle use calmodulin
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because it is very similar to troponin
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why can 50% of smooth muscle contract on their own
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due to environment around them and agents around them
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what is the smooth muscle contraction response to local tissue factors
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smooth muscle typically don't have a nerve supply so their contraction is controled via local tissue factors (lactic acid, high CO2, K, low pH, Ca)
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how do local tissue factors control the contraction of smooth muscle
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they do so by their ability to open and close channels or cause relaxation
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what is the effect of hormones on smooth muscle
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hormones (epi, nor epi, ACh) can:
change membrane potential change contractile mechanism sensitivity to Ca can release Ca from small intracellular stores (mitochondria and SR) |
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what does denervation of smooth muscle do
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it causes hypersensitivity resulting in ACh receptors all over the muscle, but DENERVATION NEVER CAUSES ATROPHY IN SMOOTH MUSCLE
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