cyclic-imp and Arterial-Occlusive-Diseases

In a number of isolated blood vessel types, hypoxia causes an acute contraction that is dependent on the presence of nitric oxide and activation of soluble guanylyl cyclase. It is more pronounced when the preparations are constricted and is therefore termed hypoxic augmentation of vasoconstriction. This hypoxic response is accompanied by increases in the intracellular level of inosine 5'-triphosphate and in the synthesis of inosine 3',5'-cyclic monophosphate (cIMP) by soluble guanylyl cyclase. The administration of exogenous cIMP or inosine 5'-triphosphate causes augmented vasoconstriction to hypoxia. Furthermore, the vasoconstriction evoked by hypoxia and cIMP is associated with increased activity of Rho kinase (ROCK), indicating that cIMP may mediate the hypoxic effect by sensitizing the myofilaments to Ca through ROCK. Hypoxia is implicated in exaggerated vasoconstriction in the pathogenesis of coronary artery disease, myocardial infarction, hypertension, and stroke. The newly found role of cIMP may help to identify unique therapeutic targets for certain cardiovascular disorders.

Topics: Animals; Arterial Occlusive Diseases; Calcium Signaling; Cyclic IMP; Endothelium, Vascular; Guanylate Cyclase; Humans; Hypoxia; Muscle, Smooth, Vascular; Receptors, Cytoplasmic and Nuclear; rho-Associated Kinases; Second Messenger Systems; Soluble Guanylyl Cyclase; Spasm; Vasoconstriction