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[线粒体三磷酸腺苷敏感性钾通道含氟激活剂对氧化磷酸化的影响]

[The influence of the fluorine-containing activators of mitochondrial adenosine triphosphate sensitive potassium channels on the oxidative phosphorilation].

作者信息

Pyvovar S M, Korzhov V I, Strutyns'kyĭ R B, Iahupol's'kyĭ L M, Moĭbenko O O

出版信息

Fiziol Zh (1994). 2006;52(3):25-33.

Abstract

The cardioprotective mechanism of KATP channel openers and especially their influence on mitochondrial respiration has not been clarified yet. In this article we investigated the effect of DiazoFm and DiazoFp, the new fluor-containing analogues of diazoxide and the potential mitochondrial KATP channel openers, on the oxidative phosphorylation in the isolated mitochondria. It was shown that the influence of KATP channel openers on ADP-stimulated oxygen consumption (State 3) depended on the substrates we used (succinate or 2-oxoglutarate sodium). We have shown that the depression of State 3 was less when we used DiazoFm (30 MM) and DiazoFp (30 MM) in comparison with Diazoxide in experiments where succinate was used. The fluor-containing KATP, channels openers did not significantly change the activity of succinate dehydrogenase in comparison with diazoxide (it decreased succinate dehydrogenase activity by 27%). Thus, the fluor-containing analogues of diazoxide did not significant influence on the complex II of the respiratory chain. In the other experiments when we used 2-oxoglutarate sodium as an oxidative substrate, DiazoFp increased ADP-stimulated oxygen consumption by 33%. All the studied KATP openers have an uncoupling effect, regardless the substrates we used. This effect was more significant when we used succinate as a substrate. We have shown that the uncoupling effect of oxidative phosphorylation is a consequence of K channels activation. This statement was proved by 5-hydroxydecanoate (200 MM) with depressed influence of Diazoxide and its fluoring-containing analogues. Conclusion. The fluor-containig KATP channels openers had not direct influence on the respiratory chain in mitochondria, but activation mitochondrial KATP channels by them lead to uncoupling phosporylation and respiration.

摘要

KATP通道开放剂的心脏保护机制,尤其是它们对线粒体呼吸的影响尚未阐明。在本文中,我们研究了二氮嗪的新型含氟类似物DiazoFm和DiazoFp以及潜在的线粒体KATP通道开放剂对分离线粒体中氧化磷酸化的影响。结果表明,KATP通道开放剂对ADP刺激的氧消耗(状态3)的影响取决于我们使用的底物(琥珀酸或2-氧代戊二酸钠)。我们已经表明,在使用琥珀酸的实验中,与二氮嗪相比,当我们使用DiazoFm(30μM)和DiazoFp(30μM)时,状态3的降低较少。与二氮嗪相比,含氟的KATP通道开放剂对琥珀酸脱氢酶的活性没有显著影响(二氮嗪使琥珀酸脱氢酶活性降低了27%)。因此,二氮嗪的含氟类似物对呼吸链的复合物II没有显著影响。在其他实验中,当我们使用2-氧代戊二酸钠作为氧化底物时,DiazoFp使ADP刺激的氧消耗增加了33%。无论我们使用何种底物,所有研究的KATP开放剂都具有解偶联作用。当我们使用琥珀酸作为底物时,这种作用更为显著。我们已经表明,氧化磷酸化的解偶联作用是K通道激活的结果。5-羟基癸酸(200μM)对二氮嗪及其含氟类似物的影响有抑制作用,这证明了这一说法。结论。含氟的KATP通道开放剂对线粒体中的呼吸链没有直接影响,但它们激活线粒体KATP通道会导致磷酸化和呼吸的解偶联。

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