Excitation and contraction of smooth muscles Flashcards
2 types of smooth muscles
multi unit and unitary smooth muscles
multi unit smooth muscles
are separate distinct smooth muscle fibers, each one of the function independently and each innervated by a single nerve ending. A basement membrane covers which is made of thin collagen and glycoprotein
e.g of multi unit smooth muscles
cilliary and iris muscles of eye, piloerector muscles of hair
unitary smooth muscles
called as visceral or syncytial smooth muscles are hundreds and thousands of smooth muscle fiber that contracts together
they are arranged in sheets and bundles and their cell membranes are adherent to one another so the contraction force can travel in the neighboring fibers
they also have gap junctions for movement of ions for action potential or without action potential
why unitary SM is called syncytial and visceral
it syncytial interconnections between fibers and is present in the walls of most viscera of the body, GIT, bile duct, uterus, ureters and many blood vessels
physical basis for smooth muscle contraction
in SM the actin filaments are attached to dense bodies, the dense bodies are either attached to cell membrane or dispersed inside the cell, membrane dense bodies are attached to adjacent cell by protein bridges and that’s how the the force of contraction is transmitted from one cell to another. interspread between the actin filaments is the myosin filaments
describe contractile unit of SM
many actin filaments radiating from two dense bodies , their ends overlap with myosin filamets midway between the dense bodies
what acts as Z disk in SM
the dense bodies
side polar
side polar cross bridges(present on myosin filament) means the crossbridge on one side hinge towards in one direction meanwhile the other bridge hinge towards the opposite so when the myosin filament pulls an actin filament it pulls one in one direction towards one side and other in the other direction on opposite side
regulation of contraction by calcium ions in SM
- the concentration of calcium ions increase in the cytosolic SM because of influx of CA from calcium channels or sarcoplasmic reticulum
- calcium ions reversibly join with calmodulin
- CA-calmodulin complex then attaches and activates the MYOSIN LIGHT CHAIN KINASE (phosphorylated enzyme)
- one of the myosin light chains of myosin head (regulatory chain) becomes phosphorylated cause of myosin kinase
- the non phosphorylated cannot attach/ detach with actin meanwhile the phosphorylated ones can
source of calcium ions in SM that causes contraction are
the calcium ions are diffused in the muscles from the extracellular fluid at the time of action potential. CA concentration in ECF is 10-3 molar and in muscles is 10-7 which allows rapid diffusion of CA ions inside
latent period
the time required for the diffusion of CA ions inside is 200-300 milliseconds before the contraction occurs which is 50 times greater for SM than in skeletal muscles
ROLE of smooth sarcoplasmic reticulum in Smooth muscles
the sarcoplasmic reticulum has caveolae which is invagination of cell membrane and is a rudimentary analog of transverse tubules
when action potential reaches the caveolae, calcium ions are released from sarco reticulum, works in same was as t transverse tubule cause release of CA from longitudinal sarc reticulum
the more extensive the sarc reticulum is the more rapidly SE contracts
smooth muscles contraction is dependent on ECF CA concentration
if the CA concentration falls in ECF to 1/3 to 1/10, the smooth muscle contraction ceases
what causes smooth muscles relaxation
in order to relax smooth muscles, ca ions must be removed from the muscles , the Ca ions are removed by the Calcium pumps back to ECF or Sarc reticulum
the calcium pumps of Smooth muscles aren’t as rapid as sarcoplasmic reticular pump of skeletal muscles so a muscle contraction continues for seconds as compare to hundredth or tenth of a second in skeletal
myosin phosphatase
when the calcium levels drop below a critical level, the process mention of calcium pumping reverse, myosin phosphatase phosphorylates the regulatory light chain, and then the cycle stops and contraction ceases
possible mechanism of regulation latching phenomena
as myosin kinase and phosphatase is highly activated, the cycling frequency of myosin head and contraction is high
so the myosin head remains attach for longer period of time with actin
even when then kinase and phosphatase decreases so does the frequency of cycling but deactivation of these enzymes allows the myosin heads to remain attach and the static force of contraction is maintained.
diffuse junction
autonomic nerve fibers that innervate the smooth muscles branches diffusely on the sheet of the muscle fiber
these nerve fibers are not in direct contact with the smooth muscle fiber but form diffused junction, release the transmitter on the matrix coat of the smooth muscle