Pharmacology of nitric oxide: Molecular mechanisms and therapeutic strategies

被引:48
作者
Domenico, R [1 ]
机构
[1] Univ Sherbrooke, Sch Med, Sherbrooke, PQ J1H 5N4, Canada
关键词
guanylate cyclase; NO; NO synthases; kallikrein-kinins; kinin receptors; NO donors; NOS inhibitors; cyclic GMP;
D O I
10.2174/1381612043384709
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
NO is considered to be an ubiquitous endogenous system which takes part in body's homeostatic regulations and in pathological events. NO derives from a) the actions of enzymes, the NO Synthases (NOS), which are constitutives (endothelial NOS (eNOS) and nervous NOS (nNOS)) and generate small amounts of NO and have homeostatic functions: and b) from the actions of inducible NOS (iNOS), which generate large amounts of NO and exert protective actions against noxious agents but also toxic effects (e.g. inhibition of enzymes) through the production of peroxynitrite (ONOO-). Modulation of the L-Arg/NO system may be used to obtain favourable therapeutic results, either by promoting (e.g. with NO donors) or by reducing (e.g. with NOS inhibitors) the production of NO. The present chapter will consider two approaches and four groups of potential therapeutic agents: 1) The stimulation or NO production with; a) agents which improve the efficiency of the Kallikrein-Kinin System; b) NO donors 2) The reduction of excessive NO production with: a) inhibitors of NO Synthases; b) agents that reduce the formation of reactive nitrogen/oxygen species (RNS/ROS).
引用
收藏
页码:1667 / 1676
页数:10
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