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琥珀酸是线粒体复合物 I 中 O2-/H2O2 释放的控制器:苹果酸负调节,氰化物正调节。

Succinate is the controller of O2-/H2O2 release at mitochondrial complex I : negative modulation by malate, positive by cyanide.

机构信息

Dipartimento di Chimica Biologica, Università di Padova, Viale Giuseppe Colombo 3, 35131, Padova, Italy.

出版信息

J Bioenerg Biomembr. 2009 Aug;41(4):387-93. doi: 10.1007/s10863-009-9238-2. Epub 2009 Oct 10.

Abstract

Mitochondrial production of H(2)O(2) is low with NAD substrates (glutamate/pyruvate, 3 and 2 mM) (G/P) and increases over ten times upon further addition of succinate, with the formation of a sigmoidal curve (semimaximal value at 290 microM, maximal H(2)O(2) production at 600 microM succinate). Malate counteracts rapidly the succinate induced increased H(2)O(2) release and moves the succinate dependent H(2)O(2) production curve to the right. Nitric oxide (NO) and carbon monoxide (CO) are cytochrome c oxidase inhibitors which increase mitochondrial ROS production. Cyanide (CN(-)) was used to mimic NO and CO. In the presence of G/P and succinate (300 microM), CN(-) progressively increased the H(2)O(2) release rate, starting at 1.5 microM. The succinate dependent H(2)O(2) production curve was moved to the left by 30 microM CN(-). The V(max) was little modified. We conclude that succinate is the controller of mitochondrial H(2)O(2) production, modulated by malate and CN(-). We propose that succinate promotes an interaction between Complex II and Complex I, which activates O(2)(-) production.

摘要

线粒体以 NAD 底物(谷氨酸/丙酮酸,3 和 2 mM)(G/P)产生的 H(2)O(2)产量较低,当进一步添加琥珀酸时,H(2)O(2)的产生增加了十倍以上,形成了一个 S 形曲线(半最大值在 290 microM,最大 H(2)O(2)产量在 600 microM 琥珀酸)。苹果酸迅速抵消了琥珀酸诱导的 H(2)O(2)释放增加,并将依赖琥珀酸的 H(2)O(2)产生曲线向右移动。一氧化氮(NO)和一氧化碳(CO)是细胞色素 c 氧化酶抑制剂,可增加线粒体 ROS 的产生。氰化物(CN(-))用于模拟 NO 和 CO。在 G/P 和琥珀酸(300 microM)存在的情况下,CN(-)逐渐增加 H(2)O(2)的释放速率,从 1.5 microM 开始。30 microM CN(-)将依赖琥珀酸的 H(2)O(2)产生曲线向左移动。V(max)几乎没有改变。我们得出结论,琥珀酸是线粒体 H(2)O(2)产生的控制器,受苹果酸和 CN(-)的调节。我们提出,琥珀酸促进复合物 II 和复合物 I 之间的相互作用,从而激活 O(2)(-)的产生。

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