Bryan Nathan S, Bian Ka, Murad Ferid
Institute of Molecular Medicine, The University of Texas-Houston Health Sciences Center, Houston, TX 77030, USA.
Front Biosci (Landmark Ed). 2009 Jan 1;14(1):1-18. doi: 10.2741/3228.
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 and cGMP-independent pathways.
一氧化氮是一种多功能信号分子,复杂地参与维持许多生理过程,包括但不限于宿主防御、神经元通讯和血管张力调节。许多最初归因于一氧化氮的生理功能是通过其主要受体可溶性鸟苷酸环化酶介导的。一氧化氮的内源性产生是一个高度复杂且受调控的过程,涉及L-精氨酸的5电子氧化,需要多种底物和辅因子。这种高反应性和可扩散自由基气体的产生,进一步使我们已确立的特异性和靶向性受体-配体相互作用以引发细胞信号事件的概念和模型变得复杂。因此,一氧化氮产生改变及随后可溶性鸟苷酸环化酶激活的内源性途径中有许多步骤可能成为药物开发的靶点,以及一氧化氮的其他分子靶点。以下综述将突出一氧化氮-可溶性鸟苷酸环化酶研究的当前技术水平,并举例说明可能受益于利用一氧化氮-可溶性鸟苷酸环化酶途径以及一氧化氮合酶和不依赖环磷酸鸟苷途径进行新药开发的疾病过程。