Schrammel A, Behrends S, Schmidt K, Koesling D, Mayer B
Institut für Pharmakologie und Toxikologie, Karl-Franzens-Universität Graz, Austria.
Mol Pharmacol. 1996 Jul;50(1):1-5.
Nitric oxide (NO) binds with high affinity to the heme of soluble guanylyl cyclase (sGC), resulting in accumulation of the second messenger cGMP in many biological systems. 1H-[1,2,4]Oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) was recently described as potent and selective inhibitor of sGC, providing an invaluable tool with which to settle the function of the cGMP pathway in NO-mediated signal transduction [Mol. Pharmacol. 48:184-188 (1995)]. The present study investigated the mechanism of ODQ-induced inhibition of purified bovine lung sGC. The drug induced a rightward shift of the concentration-response curves recorded with two different NO donors and a reduction of maximal sGC activity, pointing to a mixed type of inhibition. The time course of NO-stimulated sGC activity determined in the presence of 0.3 microM ODQ showed that the inhibitory effect was time-dependent (half-time approximately 3 min) and virtually complete after about 10 min. The cyclase did not recover from ODQ-induced inhibition upon extensive dilution, pointing to an apparently irreversible inactivation of the enzyme by the quinoxalin. Light absorbance spectroscopy showed that ODQ (0.3 mM) induced a shift of the Soret band of the heme from 431 nm to 393 nm, indicating that ODQ oxidizes the ferrous form of the enzyme to the ferric species, which is though to exhibit only poor NO sensitivity. Together, our results suggest that inhibition of sGC by ODQ is NO-competitive and results in an apparently irreversible oxidation of the prosthetic heme group.
一氧化氮(NO)与可溶性鸟苷酸环化酶(sGC)的血红素具有高亲和力,导致第二信使环磷酸鸟苷(cGMP)在许多生物系统中积累。1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)最近被描述为sGC的强效和选择性抑制剂,为确定cGMP途径在NO介导的信号转导中的功能提供了一个宝贵工具[《分子药理学》48:184 - 188(1995)]。本研究调查了ODQ诱导的对纯化牛肺sGC抑制的机制。该药物使两种不同NO供体记录的浓度 - 反应曲线向右移动,并降低了sGC的最大活性,表明是混合型抑制。在0.3微摩尔ODQ存在下测定的NO刺激的sGC活性的时间进程表明,抑制作用是时间依赖性的(半衰期约3分钟),约10分钟后几乎完全抑制。在大量稀释后,环化酶未从ODQ诱导的抑制中恢复,表明喹喔啉对该酶造成了明显不可逆的失活。吸光光谱显示ODQ(0.3毫摩尔)使血红素的Soret带从431纳米移至393纳米,表明ODQ将酶的亚铁形式氧化为铁离子形式,据认为后者对NO的敏感性较差。总之,我们的结果表明ODQ对sGC的抑制是NO竞争性的,并导致辅基血红素基团明显不可逆的氧化。