cGMP in the Vasculature.
Department of Pharmacology, Monash University, Melbourne (Clayton), VIC, 3800, Australia, .
Journal Article: Handbook of experimental pharmacology 02/2009; DOI: 10.1007/978-3-540-68964-5_19
Abstract
Cyclic guanosine 3', 5'-monophosphate (cGMP) plays an integral role in the control of vascular function. Generated from guanylate cyclases in response to the endogenous ligands, nitric oxide (NO) and natriuretic peptides (NPs), cGMP influences a number of vascular cell types and regulates vasomotor tone, endothelial permeability, cell growth and differentiation, as well as platelet and blood cell interactions. Reciprocal regulation of the NO-cGMP and NP-cGMP pathways is evident in the vasculature such that one cGMP generating system may compensate for the dysfunction of the other. Indeed, aberrant cGMP production and/or signalling accompanies many vascular disorders such as hypertension, atherosclerosis, coronary artery disease and diabetic complications. This chapter highlights the main vascular functions of cGMP, its role in disease and the resulting current and potential therapeutic applications. With respect to pulmonary hypertension, heart failure and erectile dysfunction, as well as cGMP signal transduction, the reader is specifically referred to other dedicated chapters.
Source: PubMed
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Keywords
aberrant cGMP production
blood cell interactions
cell growth
cGMP signal transduction
coronary artery disease
Cyclic guanosine 3'
dedicated chapters
endogenous ligands
erectile dysfunction
Generated
heart failure
natriuretic peptides
nitric oxide
NPs
potential therapeutic applications
Reciprocal regulation
regulates vasomotor tone
resulting current
vascular cell types

