潮间带和潮下三鳍鱼脑线粒体的电子转移和ROS生成。

Jules B L Devaux, Chris P Hedges, Nigel Birch, Neill Herbert, Gillian M C Renshaw, Anthony J R Hickey
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引用次数: 2

摘要

虽然氧是氧化磷酸化的必要条件,但当O2与线粒体电子传递系统的电子相互作用时,可以形成活性氧(reactive species, ROS)。活性氧依赖于O2压力(PO2),传统上在O2饱和介质中进行评估,在PO2下,线粒体通常在体内不起作用。呼吸复合体II底物琥珀酸盐可显著升高线粒体ROS,其可在缺氧组织中积累,并随着再氧化进一步加剧。潮间带物种反复暴露于极端的氧气波动中,并可能进化出避免过量活性氧产生的策略。研究了潮间带和潮下三鳍鱼在高氧和缺氧状态下线粒体电子渗漏和ROS生成的变化,并评估了缺氧再氧化的影响和琥珀酸浓度增加的影响。在典型的胞内PO2下,所有物种的净ROS产量相似;然而,在PO2升高时,潮间带三鳍鱼的脑组织释放的ROS比潮下鱼类少。此外,在体外缺氧再氧化后,琥珀酸滴定介导的电子转移对潮间带物种来说更有利于呼吸,而不是ROS的产生。总的来说,这些数据表明潮间带三鳍鱼物种更好地管理ETS内的电子,从缺氧到高氧过渡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Electron transfer and ROS production in brain mitochondria of intertidal and subtidal triplefin fish (Tripterygiidae).

While oxygen is essential for oxidative phosphorylation, O2 can form reactive species (ROS) when interacting with electrons of mitochondrial electron transport system. ROS is dependent on O2 pressure (PO2) and has traditionally been assessed in O2 saturated media, PO2 at which mitochondria do not typically function in vivo. Mitochondrial ROS can be significantly elevated by the respiratory complex II substrate succinate, which can accumulate within hypoxic tissues, and this is exacerbated further with reoxygenation. Intertidal species are repetitively exposed to extreme O2 fluctuations, and have likely evolved strategies to avoid excess ROS production. We evaluated mitochondrial electron leakage and ROS production in permeabilized brain of intertidal and subtidal triplefin fish species from hyperoxia to anoxia, and assessed the effect of anoxia reoxygenation and the influence of increasing succinate concentrations. At typical intracellular PO2, net ROS production was similar among all species; however at elevated PO2, brain tissues of the intertidal triplefin fish released less ROS than subtidal species. In addition, following in vitro anoxia reoxygenation, electron transfer mediated by succinate titration was better directed to respiration, and not to ROS production for intertidal species. Overall, these data indicate that intertidal triplefin fish species better manage electrons within the ETS, from hypoxic-hyperoxic transitions.

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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
51
审稿时长
3.5 months
期刊介绍: The Journal of Comparative Physiology B publishes peer-reviewed original articles and reviews on the comparative physiology of invertebrate and vertebrate animals. Special emphasis is placed on integrative studies that elucidate mechanisms at the whole-animal, organ, tissue, cellular and/or molecular levels. Review papers report on the current state of knowledge in an area of comparative physiology, and directions in which future research is needed.
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