Fock Ekaterina M, Parnova Rimma G
Sechenov Institute of Evolutionary Physiology and Biochemistry of the Russian Academy of Sciences, 194223 Saint-Petersburg, Russia.
Pharmaceutics. 2021 Jan 22;13(2):144. doi: 10.3390/pharmaceutics13020144.
Lipopolysaccharide (LPS), the major component of the outer membrane of Gram-negative bacteria, is the most abundant proinflammatory agent. Considerable evidence indicates that LPS challenge inescapably causes oxidative stress and mitochondrial dysfunction, leading to cell and tissue damage. Increased mitochondrial reactive oxygen species (mtROS) generation triggered by LPS is known to play a key role in the progression of the inflammatory response. mtROS at excessive levels impair electron transport chain functioning, reduce the mitochondrial membrane potential, and initiate lipid peroxidation and oxidative damage of mitochondrial proteins and mtDNA. Over the past 20 years, a large number of mitochondria-targeted antioxidants (mito-AOX) of different structures that can accumulate inside mitochondria and scavenge free radicals have been synthesized. Their protective role based on the prevention of oxidative stress and the restoration of mitochondrial function has been demonstrated in a variety of common diseases and pathological states. This paper reviews the current data on the beneficial application of different mito-AOX in animal endotoxemia models, in either in vivo or in vitro experiments. The results presented in our review demonstrate the promising potential of approaches based on mito-AOX in the development of new treatment strategies against Gram-negative infections and LPS per se.
脂多糖(LPS)是革兰氏阴性菌外膜的主要成分,是最丰富的促炎因子。大量证据表明,LPS刺激不可避免地会导致氧化应激和线粒体功能障碍,进而导致细胞和组织损伤。已知由LPS引发的线粒体活性氧(mtROS)生成增加在炎症反应进展中起关键作用。过量的mtROS会损害电子传递链功能,降低线粒体膜电位,并引发脂质过氧化以及线粒体蛋白质和mtDNA的氧化损伤。在过去20年中,已经合成了大量不同结构的线粒体靶向抗氧化剂(mito-AOX),它们能够在线粒体内积累并清除自由基。在多种常见疾病和病理状态下,它们基于预防氧化应激和恢复线粒体功能的保护作用已得到证实。本文综述了不同mito-AOX在动物内毒素血症模型的体内或体外实验中有益应用的当前数据。我们综述中呈现的结果表明,基于mito-AOX的方法在开发针对革兰氏阴性菌感染和LPS本身的新治疗策略方面具有广阔的潜力。