The cyclic nucleotide 3’,5’-cIMP produced by sGC is a second messenger in the vascular wall
BMC Pharmacology and Toxicology volume 16, Article number: A25 (2015)
Traditionally, only the 3’,5’-cyclic monophosphates of adenosine and guanosine (produced by adenylyl cyclase and guanylyl cyclases, respectively) are regarded as true ‘second messengers’ in the vascular wall, despite the presence of other cyclic nucleotides in different tissues. Among these non-canonical cyclic nucleotides, inosine 3’,5’?cyclic monophosphate (cIMP) is synthesized by soluble guanylyl cyclase in porcine coronary arteries in response to hypoxia, when the enzyme is activated by endothelium-derived nitric oxide. Its production is associated with augmentation of vascular contraction mediated by stimulation of Rho kinase. Similar endothelium-dependent, NO-dependent and soluble guanylyl cyclase-dependent contractions can be evoked with thymoquinone, which also augments the levels of cIMP. Based on these findings, cIMP appears to meet most, if not all, of the criteria required for it to be accepted as a ‘second messenger’, at least in the vascular wall. The understanding of the role of this non-canonical cyclic nucleotide may help identifying novel therapeutic targets for certain cardiovascular disorders, in particular those associated with sleep apnea.
About this article
Cite this article
Vanhoutte, P.M., Leung, S.W. & Gao, Y. The cyclic nucleotide 3’,5’-cIMP produced by sGC is a second messenger in the vascular wall. BMC Pharmacol Toxicol 16 (Suppl 1), A25 (2015). https://doi.org/10.1186/2050-6511-16-S1-A25