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羧基苍术苷抑制游离脂肪酸的解偶联作用。

Carboxyatractylate inhibits the uncoupling effect of free fatty acids.

作者信息

Bondareva T O, Dedukhova V I, Mokhova E N, Skulachev V P, Volkov N I

机构信息

A.N. Belozersky Laboratory of Molecular Biology and Bioorganic Chemistry, Moscow State University, USSR.

出版信息

FEBS Lett. 1988 Jan 4;226(2):265-9. doi: 10.1016/0014-5793(88)81436-4.

Abstract

The ATP/ADP-antiporter inhibitors and ADP decrease the palmitate-induced stimulation of the mitochondrial respiration in the controlled state. The degree of inhibition decreases in the order: carboxyatractylate greater than bongkrekic acid, palmitoyl-CoA, ADP greater than atractylate. GDP is ineffective. The inhibiting concentration of carboxyatractylate coincides with this arresting the state 3 respiration. Carboxyatractylate inhibition decreases when the palmitate concentration increases. Stimulation of controlled respiration by FCCP or gramicidin D at any concentration of these uncouplers is carboxyatractylate-resistant, whereas that by low concentrations of DNP is partially suppressed by carboxyatractylate. These data together with observations that palmitate does not increase H+ conductance in bilayer phospholipid membranes and in cytochrome oxidase-asolectin proteoliposomes indicate that the ATP/ADP-antiporter is somehow involved in the uncoupling by low concentrations of fatty acids (or DNP), whereas that by FCCP and gramicidin D is due to their effect on the phospholipid bilayer. It is suggested that the antiporter facilitates translocation of palmitate anion across the mitochondrial membrane.

摘要

ATP/ADP 反向转运体抑制剂和 ADP 在对照状态下可降低棕榈酸酯诱导的线粒体呼吸刺激。抑制程度按以下顺序降低:羧基苍术苷大于 Bongkrekic 酸、棕榈酰辅酶 A、ADP 大于苍术苷。GDP 无效。羧基苍术苷的抑制浓度与阻止状态 3 呼吸的浓度一致。当棕榈酸酯浓度增加时,羧基苍术苷的抑制作用减弱。在这些解偶联剂的任何浓度下,FCCP 或短杆菌肽 D 对对照呼吸的刺激对羧基苍术苷具有抗性,而低浓度 DNP 引起的刺激则被羧基苍术苷部分抑制。这些数据以及棕榈酸酯不会增加双层磷脂膜和细胞色素氧化酶 - 大豆卵磷脂蛋白脂质体中 H⁺ 传导性的观察结果表明,ATP/ADP 反向转运体以某种方式参与低浓度脂肪酸(或 DNP)引起的解偶联作用,而 FCCP 和短杆菌肽 D 引起的解偶联作用则归因于它们对磷脂双层的影响。有人提出,反向转运体促进棕榈酸酯阴离子穿过线粒体膜的转运。

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