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花生四烯酸酰胺抑制分离的肝线粒体的氧化磷酸化。

Anandamide inhibits oxidative phosphorylation in isolated liver mitochondria.

机构信息

Department of Medical Biochemistry, Biology and Physics, University of Bari, Policlinico, Bari, Italy.

出版信息

FEBS Lett. 2011 Jan 21;585(2):429-34. doi: 10.1016/j.febslet.2010.12.032. Epub 2010 Dec 25.

Abstract

A study on the effect of anandamide (AEA) in energy coupling of rat liver mitochondria is presented. Micromolar concentrations of AEA, while almost ineffective on substrate supported oxygen consumption rate and on uncoupler stimulated respiration, strongly inhibited the respiratory state III. AEA did not change the rate and the extent of substrate generated membrane potential, but markedly delayed rebuilding by respiration of the potential collapsed by ADP addition. Overall, these data suggest that anandamide inhibits the oxidative phosphorylation process. Direct measurement of the F(o)F(1) ATP synthase activity showed that the oligomycin sensitive ATP synthesis was inhibited by AEA, (IC(50), 2.5 μM), while the ATP hydrolase activity was unaffected. Consistently, AEA did not change the membrane potential generated by ATP hydrolysis.

摘要

本文研究了大麻素(AEA)在大鼠肝线粒体能量偶联中的作用。毫摩尔浓度的 AEA 对底物支持的耗氧速率和解偶联剂刺激的呼吸几乎没有作用,但强烈抑制呼吸状态 III。AEA 没有改变由底物产生的膜电位的速率和幅度,但明显延迟了由 ADP 添加引起的电位崩溃的呼吸重建。总的来说,这些数据表明大麻素抑制氧化磷酸化过程。直接测量 F(o)F(1)ATP 合酶活性表明,AEA 抑制寡霉素敏感的 ATP 合成(IC(50),2.5 μM),而 ATP 水解酶活性不受影响。一致地,AEA 不改变由 ATP 水解产生的膜电位。

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