Shigematsu M L, Uno J, Arai T
Antimicrob Agents Chemother. 1982 Jun;21(6):919-24. doi: 10.1128/AAC.21.6.919.
Ketoconazole, an oral antimycotic imidazole drug, blocked the transport of electrons in the respiratory chain of Candida albicans under aerobic conditions with different substrates, such as NADH and succinate. This effect was a nonspecific inhibition of NADH oxidases and succinate oxidases. The addition of ketoconazole to C. albicans mitochondria without a substrate resulted in strong reduction of cytochrome a3, as revealed by difference spectra (reduced versus oxidized). This indicated that there was a specific interaction between ketoconazole and cytochrome c oxidase. A spectrophotometric analysis confirmed that the cytochrome oxidases other than cytochrome c oxidase were not inhibited because subsequent addition of any substrate caused an increased level of reduction of all of the other respiratory chain components compared with the control. Consequently, our data strongly suggested that the primary site of ketoconazole inhibition on isolated mitochondria from C. albicans is the most distal portion of the respiratory chain.
酮康唑是一种口服抗真菌咪唑类药物,在有氧条件下,它能与不同底物(如NADH和琥珀酸)一起阻断白色念珠菌呼吸链中的电子传递。这种作用是对NADH氧化酶和琥珀酸氧化酶的非特异性抑制。在没有底物的情况下,向白色念珠菌线粒体中添加酮康唑会导致细胞色素a3显著还原,这通过差光谱(还原态与氧化态)得以揭示。这表明酮康唑与细胞色素c氧化酶之间存在特异性相互作用。分光光度分析证实,除细胞色素c氧化酶外的其他细胞色素氧化酶未受抑制,因为随后添加任何底物都会使所有其他呼吸链成分的还原水平相对于对照有所增加。因此,我们的数据有力地表明,酮康唑对白色念珠菌分离线粒体的主要抑制位点是呼吸链的最远端部分。