Moreno-Sánchez R, Hogue B A, Bravo C, Newman A H, Basile A S, Chiang P K
Instituto Nacional de Cardiología, México, DF.
Biochem Pharmacol. 1991 May 15;41(10):1479-84. doi: 10.1016/0006-2952(91)90564-l.
The effects, of the benzodiazepines RO5-4864, AHN 086, PK 11195 and clonazepam on respiration of mitochondria from heart, kidney, and liver were studied. ADP-stimulated respiration of heart mitochondria was the most sensitive to inhibition by AHN 086; clonazepam was not inhibitory. Several respiratory chain segment activities of submitochondrial particles were insensitive to AHN 086, except for NADH oxidase which was partially inhibited. However, in contrast to submitochondrial particles, the succinate-cytochrome c oxidoreductase activity in intact mitochondria was inhibited by AHN 086, suggesting an effect at the substrate transport level. Phosphate-induced, succinate-dependent swelling was also inhibited by AHN 086 it was not affected by clonazepam. Uncoupled ATP hydrolysis was partially inhibited by RO5-4864, AHN 086, and clonazepam. It is suggested that there is an unspecific inhibition of NADH oxidase and ATP hydrolysis by these benzodiazepines and a specific inhibition on oxidizable substrate transport by the peripheral-type benzodiazepine AHN 086.
研究了苯二氮䓬类药物RO5 - 4864、AHN 086、PK 11195和氯硝西泮对心脏、肾脏和肝脏线粒体呼吸的影响。AHN 086对ADP刺激的心脏线粒体呼吸抑制作用最为敏感;氯硝西泮无抑制作用。亚线粒体颗粒的几种呼吸链片段活性对AHN 086不敏感,只有NADH氧化酶受到部分抑制。然而,与亚线粒体颗粒不同,AHN 086可抑制完整线粒体中的琥珀酸 - 细胞色素c氧化还原酶活性,提示其作用于底物转运水平。AHN 086还可抑制磷酸盐诱导的、琥珀酸依赖性肿胀,而氯硝西泮对此无影响。RO5 - 4864、AHN 086和氯硝西泮可部分抑制解偶联ATP水解。提示这些苯二氮䓬类药物对NADH氧化酶和ATP水解存在非特异性抑制,而外周型苯二氮䓬类药物AHN 086对可氧化底物转运存在特异性抑制。