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smooth muscle cells
spindle shaped, uninucleate cells with a smooth appearance
lack troponin and T tubules
intermediate filaments
form cytoskeleton non contractile cells in the smooth muscle cell
dense bodies
form cytoskeleton, actin attaches to these
Vascular category
blood vessel walls, except capillaries
gastrointestinal category
walls of digestive tract and associated organs
urinary category
wall of bladder and ureters
respiratory category
airway passages, changes diameter in airways
reproductive category
uterus in females and other reproductive structures in males and females
ocular category
iris and ciliary body, not for physically moving the eyes
contraction pattern type 1
a phasic smooth muscle that is normally relaxed and only contracts when needed
Ex. esophagus
contraction pattern type 2
a phasic smooth muscle that cycles between contraction and relaxation with low amounts of contraction
contraction pattern type 3
a tonic smooth muscle that is usually contracted, remains contracted unless to let something pass
contraction pattern type 4
a tonic smooth muscle whos contraction is varied when needed. always some level of contraction
unitary smooth muscle
contains gap junctions, allows coordinated contraction of many cells causing muscle to contract as a single unit
multiunit smooth muscle
not electrically couplesd
smooth muscles in eye, male reproductive tract and in the uterus
smooth muscle innervation
usually innervated by the autonomic nervous system and can be innervated by multiple neurons capable of releasing different neurotransmiiters
Smooth muscle ap types
brief spikes, and plateaus
contraction without action potentials
autonomic neurons create a local depolarization that spreads electronically throughout the muscle fibre triggering Ca2+ entry
single unit action potentials
autonomic AP initiation (spikes or plateaus)
spontaneous AP (slow wave or pacemaker)
electromechanical coupling
contraction due to a change in the membrane potential
Ca entry through voltage gated channels
smooth muscle cells respond to graded stimulation or action potentials, both of which produce an influx of Ca2+ through voltage gated L type Ca channels
Calcium release from the SR
Occurs via Ca2+ induced Ca release and the IP3 pathway
IP3 pathway can cause contraction with minimal depolarization and negligible extracellular Ca2+ influx
Calcium entry through voltage independent channels
depletion of Ca2+ in the SR activates store operated channels which cause a Ca2+ influx across the cell membrane. Allows calcium to remain elevated and replenishes SR
pharmacomechanical coupling
Ca2+ release from SR via IP3 pathway and entry of Ca2+ via store operated channels that are voltage dependent
stretch activated contraction
there are stretch activated ion channels in the cell membrane of some smooth muscle that when activated lead to depolarization
Calcium signal in myosin head
phosphorylates the regulatory lite chain which turns on the myosin ATPase
calmodulin
a Ca2+ binding protein similar to troponin C of striated muscle
myosin light chain kinase
phosphorylates the regulatory light chain near the myosin head which alters the conformation of the head, increasing its ATPase activity and allows it to interact with actin
Cross bridge cycling
the same as skeletal muscle but it is much slower and cell crumples up instead of shortening in a uniform fashion
relaxation of smooth muscle
the regulatory light chain must be dephosphorylated by myosin light chain phosphatase
latch state
after dephosphorylation of regulatory light chain some smooth muscle can maintain force for an extended period of time with little ATP use
increasing contractile force through calcium
MLC phosphorylation is regulated by the Ca-CaM complex, which depends on levels of intracellular Ca
contractile control by regulating Ca
sensitivity of proteins to Ca regulates contraction
inhibiting MLCP or activated MLCK leading to greater contraction at lower Ca levels