smooth muscle structure and function Flashcards
Provide examples of smooth muscles and their function in different organs
Phasic: rhythmic; seen in sphincters, esophagus, urinary blader
Tonic: continuous activity; respiratory airways and blood vessels
Describe single vs mutli unit smooth muscle
Multi-unit: muscle cells behave as individuals. These are usually involved in finer movements, such as lens and ciliary function in the eye, and in arrector pili of the skin
Single unit: muscle cells act as a group; this relies on gap junctions! This allows for coordinated contraction. This is seen in the smooth muscle of the GI tract in peristaltic contractions
Contraction is regulated by ___ filaments
thick
Describe caveoli
Invaginations of the sarcolemma that are open to the extracellular space; they’re thought to allow for expansion of the cell membrane.
What thin filaments are present in smooth muscle?
Actin and tropomyosin, no troponin
Describe the organization of thick and thin filaments in smooth muscle
Small groups of thick filaments are surrounded by many thin filaments to form a contractile unit.
What are dense bodies? Where are they found? What connects them to each other?
Sites of attachment for thin filaments; they’re found in the sarcolemma and in the cytoplasm; intermediate filaments such as desmin and vimentin
What junction type mechanically connects muscle cells
Adherens junctions
Describe the role of different pathways and factors in the initiation and regulation of
smooth muscle contraction
Can be controlled by autonomic control, circling hormones, electronic coupling, locally generated signaling molecules, or intrinsic electrical activity
Describe the steps leading to cross-bridge cycling in smooth muscle
-Calcium binds to calmodulin
-Calcium-calmodulin activates MLCK
-MLCK phosphorylates myosin
-Myosin can attach to actin
-ADP AND PI dissociate from the myosin head and contraction can happen
-ATP binds the myosin head, releasing actin and relaxing the muscle
Describe myosin phosphatase
Myosin phosphatase removes the phosphate from the myosin, releasing actin filaments and stopping contraction
Describe pharmacomechanical coupling and its physiological significance
Impacts contraction without changing membrane potential; this is usually receptor specific and may or may not use calcium
Give examples of ligands capable of calcium mediated pharamcomechanical coupling
Examples capable of this include norepinephrine, angiotensin, and vasopressin
Describe calcium mediated pharmacomechanical coupling
Activation of phospholipase C, forming IP3 and DAG. IP3 increases calcium cytosolic concentration, which can increase contraction. Store-activate channels will be activated to bring extracellular calcium into the sarcoplasmic reticulum, and SERCA will remove calcium from the cytosol to maintain the decrease and increase of calcium needed for contraction.
Describe how cAMP regulates pharmacomechanical coupling
-Lowering MLCLK activity: cAMP is decreased, lowering MLCK phosphorylation and thus its activity. This leads to muscle relaxation. Ligand examples include norepinephrine, adenosine, and b2 agonists