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呋塞米对线粒体电子传递系统和氧化磷酸化的影响。

Effect of furosemide on mitochondrial electron transport system and oxidative phosphorylation.

作者信息

Orita Y, Fukuhara Y, Yanase M, Ando A, Okada N, Abe H

出版信息

Arzneimittelforschung. 1983;33(10):1446-50.

PMID:6316993
Abstract

The effects of furosemide on the mitochondrial electron transport system and on oxidative phosphorylation were explored. Furosemide above the concentration of 2 X 10(-3) mol/l was found to inhibit state 3 (ADP-dependent) respiration of the rat liver, renal cortex, renal medulla mitochondria. State 4 (resting) respiration was not affected by furosemide. Furosemide above the concentration of 7.5 X 10(-6) mol/l (substrate: glutamate-malate), and above 5 X 10(-6) mol/l (substrate: succinate) inhibited the respiration of rat liver mitochondria released by 3,5-di-tert-butyl-4-hydroxybenzylidenemalononitrile (SF 6847). This fact exactly indicates that furosemide inhibits the electron transport system in mitochondria. Furosemide at the concentration of 4 X 10(-3) mol/l inhibited the activities of NADH cytochrome c reductase and succinate cytochrome c reductase in sonicated mitochondrial subparticles of beef heart by 78.2% and 79.2% of control, respectively.

摘要

研究了呋塞米对线粒体电子传递系统和氧化磷酸化的影响。发现浓度高于2×10⁻³mol/L的呋塞米可抑制大鼠肝脏、肾皮质、肾髓质线粒体的状态3(ADP依赖性)呼吸。状态4(静息)呼吸不受呋塞米影响。浓度高于7.5×10⁻⁶mol/L(底物:谷氨酸-苹果酸)以及高于5×10⁻⁶mol/L(底物:琥珀酸)的呋塞米可抑制3,5-二叔丁基-4-羟基苄叉丙二腈(SF 6847)释放的大鼠肝脏线粒体的呼吸。这一事实确切表明呋塞米抑制线粒体中的电子传递系统。浓度为4×10⁻³mol/L的呋塞米分别使牛心脏超声破碎线粒体亚颗粒中NADH细胞色素c还原酶和琥珀酸细胞色素c还原酶的活性比对照降低78.2%和79.2%。

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