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Smooth Muscle SG
Smooth Muscle
| Question | Answer |
|---|---|
| Name the 2 major extremes of smooth muscle | Unitary (same as visceral) and multiunit. In unitary the cells are very close together and contract in an extremely coordinated manner. |
| EDRF | Enoothelium derived relaxing factor very much in the region where neurotransmitters are released |
| Does smM have the ability to down regulate its energy? | Yes. So it can maintain high levels of force w/o using too much energy. It can generate a lot of force even with anaerobic oxidation |
| What are the dense bodies attachment for? | Thin filaments |
| What are the thick filaments used for? | Actin, myosin interaction. Sliding filament mechanism |
| Name thin filament associated proteins | Actin, Tropomyosin, Caldesmin, Calponin and Calmodulin |
| Name thick filament associated proteins | Myosin heavy and light chain and MLCK |
| What is equivalent to Troponin I and C in smM? | Caldesmin and Calponin= Troponin I and Calmodulin= Troponin C |
| What phosphorylates the Myosin light chains? | MLC kinase. This causes increase in force and ATP consumption/ ATPase activity caused by the myosin-actin interaction to generate force. Kinase is stimulated by calcium-calmodulin |
| What phosphorylates MLCK? | PKA and this leads to decrease in calcium action |
| MLC phosphatase | Dephosphorylated MLC which turns off process |
| Name 2 systems that act as pro-contractile mechanism in signaling | Protein Kinase C and Rho kinase system |
| What is MLCK a target for? | cAMP signaling. cAMP is one of the mechanisms of relaxation. PKA can phosphorylate MLCK and sort of inhibit MLCK |
| Describe the receptor mechanism involving PLC | Generates IP3 and DAG. IP3 enhances contractive apparatus and DAG is primary stimulator of PKC which leads to increase action of Ca |
| Describe SERCA pump | Reuptake mechanism. Phosphorylated by cAMP and cGMP kinase which leads to more Ca pumped back into SR |
| Describe visceral/unitary smM | May have gap junctions b/w cells. If there is no gap junctions mechanical connections will lead to contraction of cell due to contraction of adjacent cell. |
| Pacemaker cell of visceral smM | First cell in stretching process that when muscle depolarizes it promotes contraction in adjacent cells. Then propogation |
| SNS-regulated smM | Alpha and beta receptors. alpha1 and beta2 are primary. alpha receptors work in direction of increase force, sensitive to NE. beta works in decrease, sensitive to Epi |
| How does alpha1 receptor work? | Via receptor operated release of Ca to generate force |
| How does beta2 receptor work? | Biggest stimulus is epi activating adenylate cyclase to make cAMP. (beta is enhanced in vascular smM) |
| PSNS regulated smM | Uses Ach and Ach acts on muscarine receptors, activate to increase force. Direct effect of smM is to work via ROC mechanism to increase the force |
| Tissue hormone regulated smM | Endothelium is enriched with NO synthase and converts L-Arginine to NO. PGI2 is made in endothelium. |
| What channels do ENHF open? | K channels that hyperpolarize and there is hydrogen peroxide |
| Metabolic Regulation | Circulation deals with oxygen delivery attempting to match oxygen demand/use. You release lactate during anaerobic oxidation which activates smM to relax. |