Ricoux Rémy, Boucher Jean-Luc, Mandon Dominique, Frapart Yves-Michel, Henry Yann, Mansuy Daniel, Mahy Jean-Pierre
Laboratoire de Chimie Bioorganique et Bioinorganique, Institut de Chimie Moléculaire d'Orsay, Université Paris-Sud XI, Orsay, France.
Eur J Biochem. 2003 Jan;270(1):47-55. doi: 10.1046/j.1432-1033.2003.03358.x.
Nitric oxide (NO) is a potent intra- and intercellular messenger involved in the control of vascular tone, neuronal signalling and host response to infection. In mammals, NO is synthesized by oxidation of l-arginine catalysed by hemeproteins called NO-synthases with intermediate formation of Nomega-hydroxy-l-arginine (NOHA). NOHA and some hydroxyguanidines have been shown to be able to deliver nitrogen oxides including NO in the presence of various oxidative systems. In this study, NOHA and a model compound, N-(4-chlorophenyl)-N'-hydroxyguanidine, were tested for their ability to generate NO in the presence of a haemprotein model, microperoxidase 8 (MP8), and hydrogen peroxide. Nitrite and nitrate production along with selective formation of 4-chlorophenylcyanamide was observed from incubations of N-(4-chlorophenyl)-N'-hydroxyguanidine in the presence of MP8 and hydrogen peroxide. In the case of NOHA, the corresponding cyanamide, Ndelta-cyano-L-ornithine, was too unstable under the conditions used and l-citrulline was the only product identified. A NO-specific conversion of 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide to 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl and formation of MP8-Fe-NO complexes were observed by EPR spectroscopy and low-temperature UV/visible spectroscopy, respectively. These results clearly demonstrate the formation of nitrogen oxides including NO from the oxidation of exogenous hydroxyguanidines by hydrogen peroxide in the presence of a minienzyme such as MP8. The importance of the bioactivation of endogenous (NOHA) or exogenous N-hydroxyguanidines by peroxidases of physiological interest remains to be established in vivo.
一氧化氮(NO)是一种强大的细胞内和细胞间信使,参与血管张力控制、神经信号传导以及宿主对感染的反应。在哺乳动物中,NO由称为一氧化氮合酶的血红素蛋白催化L-精氨酸氧化合成,中间形成Nω-羟基-L-精氨酸(NOHA)。已表明,在各种氧化系统存在下,NOHA和一些羟基胍能够释放包括NO在内的氮氧化物。在本研究中,测试了NOHA和一种模型化合物N-(4-氯苯基)-N'-羟基胍在血红素蛋白模型微过氧化物酶8(MP8)和过氧化氢存在下产生NO的能力。在MP8和过氧化氢存在下孵育N-(4-氯苯基)-N'-羟基胍时,观察到亚硝酸盐和硝酸盐的产生以及4-氯苯基氰胺的选择性形成。就NOHA而言,相应的氰胺Nδ-氰基-L-鸟氨酸在所使用的条件下过于不稳定,并且L-瓜氨酸是唯一鉴定出的产物。分别通过电子顺磁共振光谱和低温紫外/可见光谱观察到2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧基3-氧化物向2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧基的NO特异性转化以及MP8-Fe-NO配合物的形成。这些结果清楚地证明了在诸如MP8的微酶存在下,过氧化氢将外源性羟基胍氧化形成包括NO在内的氮氧化物。内源性(NOHA)或外源性N-羟基胍通过具有生理意义的过氧化物酶进行生物活化的重要性仍有待在体内确定。