Discovery of the nitric oxide signaling pathway and targets for drug development

被引:171
作者
Bryan, Nathan S. [1 ]
Bian, Ka [1 ,2 ,3 ]
Murad, Ferid [1 ,2 ,3 ]
机构
[1] Univ Texas Houston, Hlth Sci Ctr, Inst Mol Med, Houston, TX 77030 USA
[2] Shanghai Univ, Murad Res Inst Modernized Chinese Med, Shanghai, Peoples R China
[3] Shanghai Univ E Res Inst, Nitr Oxide & Inflammatory Med, Shanghai, Peoples R China
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
关键词
Nitric Oxide; cyclicGMP; soluble guanylyl cyclase; Nitrogen Species; Cardiovascular system; Nitrite; Nitrate; Diet; Review; SOLUBLE GUANYLYL CYCLASE; VASCULAR SMOOTH-MUSCLE; CYCLIC GUANOSINE-MONOPHOSPHATE; L-ARGININE; S-NITROSYLATION; DIETARY NITRATE; ISCHEMIA-REPERFUSION; DOWN-REGULATION; IN-VIVO; ANTIINFLAMMATORY PROPERTIES;
D O I
10.2741/3228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nitric oxide is a multifunctional signaling molecule, intricately involved with maintaining a host of physiological processes including but not limited to host defense, neuronal communication and the regulation of vascular tone. Many of the physiological functions first ascribed to NO are mediated through its primary receptor, soluble guanylyl cyclase. Endogenous production of NO is a highly complex and regulated process involving the 5-electron oxidation of L-arginine requiring numerous substrates and cofactors. The production of a highly reactive and diffusible free radical gas further complicates our established concept and model of specific and targeted receptor-ligand interaction to elicit cell signaling events. Hence there are many steps in the endogenous pathway for altered production of NO and subsequent activation of sGC that may be targets for drug development as well as other molecular targets for NO. The following review will highlight the current state of the art of NO-sGC research and illustrate disease processes which may benefit from novel drug development exploiting the NO-sGC pathway as well as NOS & cGMP-independent pathways.
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页码:1 / +
页数:20
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