Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Institutskaya 3, Pushchino, Moscow Region 142290, Russia; Mari State University, pl. Lenina 1, Yoshkar-Ola, Mari El 424001, Russia.
Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Institutskaya 3, Pushchino, Moscow Region 142290, Russia.
Biochim Biophys Acta Biomembr. 2019 Jan;1861(1):288-297. doi: 10.1016/j.bbamem.2018.06.012. Epub 2018 Jun 18.
The paper considers the effects of bedaquiline (BDQ), an antituberculous preparation of the new generation, on rat liver mitochondria. It was shown that 50 μM BDQ inhibited mitochondrial respiration measured with substrates of complexes I and II (glutamate/malate and succinate/rotenone systems respectively) in the states V and V. At the same time, at concentrations below 50 μM, BDQ slightly stimulated respiration with substrates of complex I in the state V. BDQ was also found to suppress, in a dose-dependent manner, the activity of complex II and the total activity of complexes II + III of the mitochondrial transport chain. It was discovered that at concentrations up to 10 μM, BDQ inhibited HO production in mitochondria. BDQ (10-50 μM) suppressed the opening of Ca-dependent CsA-sensitive mitochondrial permeability transition pore. The latter was revealed experimentally as the inhibition of Ca/P-dependent swelling of mitochondria, suppression of cytochrome c release, and an increase in the Ca capacity of the organelles. BDQ also decreased the rate of mitochondrial energy-dependent K transport, which was evaluated by the energy-dependent swelling of mitochondria in a K buffer and DNP-induced K efflux from the organelles. The possible mechanisms of BDQ effect of rat liver mitochondria are discussed.
本文研究了新一代抗结核药物贝达喹啉(BDQ)对大鼠肝线粒体的影响。结果表明,50µM 的 BDQ 抑制了线粒体呼吸,其测量底物分别为复合体 I 和 II 的底物(分别为谷氨酸/苹果酸和琥珀酸/鱼藤酮系统)在状态 V 和 V。同时,在低于 50µM 的浓度下,BDQ 略微刺激了复合体 I 在状态 V 下的呼吸。还发现 BDQ 以剂量依赖的方式抑制了线粒体 II 复合体的活性和 II+III 复合体的总活性。发现 BDQ 在浓度高达 10µM 时抑制线粒体 HO 的产生。BDQ(10-50µM)抑制了 Ca 依赖性 CsA 敏感的线粒体通透性转换孔的开放。后者通过线粒体的 Ca/P 依赖性肿胀的抑制、细胞色素 c 释放的抑制和细胞器的 Ca 容量的增加来在实验中显示。BDQ 还降低了线粒体能量依赖性 K 转运的速率,这可以通过线粒体在 K 缓冲液中的能量依赖性肿胀和 DNP 诱导的细胞器中 K 外流来评估。讨论了 BDQ 对大鼠肝线粒体作用的可能机制。