Aktan Fugen
Faculty of Pharmacy, Building A15, Room N257, University of Sydney, Sydney, NSW 2006, Australia.
Life Sci. 2004 Jun 25;75(6):639-53. doi: 10.1016/j.lfs.2003.10.042.
This review focuses on the production of nitric oxide (NO) by inducible nitric oxide synthase (iNOS) and its regulation under physiological and pathophysiological conditions. NO is an important biological mediator in the living organism that is synthesized from L-arginine using NADPH and molecular oxygen. However, the overproduction of NO which is catalyzed by iNOS, a soluble enzyme and active in its dimeric form, is cytotoxic. Immunostimulating cytokines or bacterial pathogens activate iNOS and generate high concentrations of NO through the activation of inducible nuclear factors, including NFkB. iNOS activation is regulated mainly at the transcriptional level, but also at posttranscriptional, translational and postranslational levels through effects on protein stability, dimerization, phosphorylation, cofactor binding and availability of oxygen and L-arginine as substrates. The prevention of the overproduction of NO in the living organism through control of regulatory pathways may assist in the treatment of high NO-mediated disorders without changing physiological levels of NO.
本综述聚焦于诱导型一氧化氮合酶(iNOS)产生一氧化氮(NO)及其在生理和病理生理条件下的调节。NO是生物体内一种重要的生物介质,它由L-精氨酸利用NADPH和分子氧合成。然而,由iNOS催化产生的过量NO具有细胞毒性,iNOS是一种可溶性酶,以二聚体形式具有活性。免疫刺激细胞因子或细菌病原体激活iNOS,并通过激活包括NFkB在内的诱导性核因子产生高浓度的NO。iNOS的激活主要在转录水平受到调节,但也在转录后、翻译和翻译后水平受到调节,其方式包括影响蛋白质稳定性、二聚化、磷酸化、辅因子结合以及作为底物的氧和L-精氨酸的可用性。通过控制调节途径来防止生物体内NO的过量产生,可能有助于治疗由高NO介导的疾病,而不改变NO的生理水平。