Hargreaves Iain P, Al Shahrani Mesfer, Wainwright Luke, Heales Simon J R
Neurometabolic Unit. Box 105, National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK.
Department of Molecular Neuroscience, Institute of Neurology, University College London, Queen Square, London, UK.
Drug Saf. 2016 Jul;39(7):661-74. doi: 10.1007/s40264-016-0417-x.
The mitochondrial respiratory chain (MRC) and ATP synthase (complex V) play an essential role in cellular energy production by the process of oxidative phosphorylation. In addition to inborn errors of metabolism, as well as secondary causes from disease pathophysiology, an impairment of oxidative phosphorylation can result from drug toxicity. These 'off-target' pharmacological effects can occur from a direct inhibition of MRC enzyme activity, an induction of mitochondrial oxidative stress, an uncoupling of oxidative phosphorylation, an impairment of mitochondrial membrane structure or a disruption in the replication of mitochondrial DNA. The purpose of this review is to focus on the off-target mitochondrial toxicity associated with both commonly used pharmacotherapies and a topical 'weight loss' agent. The mechanisms of drug-induced mitochondrial impairment will be discussed together with putative therapeutic strategies to counteract the adverse effects of the pharmacotherapy.
线粒体呼吸链(MRC)和ATP合酶(复合体V)在通过氧化磷酸化过程进行的细胞能量产生中起着至关重要的作用。除了先天性代谢缺陷以及疾病病理生理学的继发原因外,氧化磷酸化受损还可能由药物毒性引起。这些“脱靶”药理效应可源于对MRC酶活性的直接抑制、线粒体氧化应激的诱导、氧化磷酸化的解偶联、线粒体膜结构的损伤或线粒体DNA复制的中断。本综述的目的是关注与常用药物疗法和一种局部“减肥”药物相关的脱靶线粒体毒性。将讨论药物诱导的线粒体损伤机制以及抵消药物疗法不良反应的推定治疗策略。