Smooth muscle physiology Flashcards
Four different types of smooth muscle
Single unit, multi-unit, phasic, tonic
Caveolae
Represent invaginations of the sarcolemma; similar to T-tubules in smooth muscle
Gap junctions in smooth muscle
Allow for electrical coupling and chemical communication
Latch-bridge
Controversial structure that allows for muscles to be tonically activated for long periods of time with minimal effort
Two enzymes involved in de/phosphorylating myosin
Myosin-light-chain kinase and myosin-light-chain phosphatase
Variations of basal tone in smooth muscle
Normally contracted (sphincters) Normally partially contracted (tone) Phasically active (stomach, intestines) Normally relaxed (esophagus, bladder)
Difference between single unit and multi-unit smooth muscle cells
Single unit: they’re all connected and one receptor for neurotransmitters on one cell can propagate to many different cells.
Multi-unit: each individual cell has receptors that will act individually from the cell next to it
What allows the calcium signal to be propagated from one cell to the next in a single-unit system?
Gap junctions between cells
Function of IP3
Causes release of calcium from the sarcoplasmic reticulum via IP3 receptors, leading to MLCK-dependent contraction via Ca2+-calmodulin
What does cAMP stimulate PKA to do?
Phosphorylate MLCK to decrease its Ca2+ sensitivity, and increases sarcoplasmic reticulum calcium pumping
What does cGMP do in smooth muscle?
Stimulates MLC phsphatase, decreasing myofilament activation, which relaxes the muscle
What is cGMP associated with in muscle relaxation?
Nitric oxide (especially in vascular smooth muscle)
Describe the catch-22 of ACh in smooth muscle.
In endothelial cells, if ACh attaches, then the endothelial cells will release NO into the bloodstream and stimulate relaxation. However, if the ACh directly attaches to AChR’s in the absence of endothelium, then it will stimulate contraction.
Pathways that do not require membrane depolarization
Hormone receptor stimulation leading to formation of IP3, cAMP, cGMP, or the activation of a ligand operated Ca2+ channel
Pathways that do require alterations in membrane potential
Depolarization-induced Ca2+ entry into smooth muscle cells