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大麻素引起的脑线粒体电子传递链复合物活性变化。

Cannabinoid-Induced Changes in the Activity of Electron Transport Chain Complexes of Brain Mitochondria.

作者信息

Singh Namrata, Hroudová Jana, Fišar Zdeněk

机构信息

Department of Psychiatry, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Ke Karlovu 11, 120 00, Prague 2, Czech Republic.

出版信息

J Mol Neurosci. 2015 Aug;56(4):926-931. doi: 10.1007/s12031-015-0545-2. Epub 2015 Mar 29.

Abstract

The aim of this study was to investigate changes in the activity of individual mitochondrial respiratory chain complexes (I, II/III, IV) and citrate synthase induced by pharmacologically different cannabinoids. In vitro effects of selected cannabinoids on mitochondrial enzymes were measured in crude mitochondrial fraction isolated from pig brain. Both cannabinoid receptor agonists, Δ(9)-tetrahydrocannabinol, anandamide, and R-(+)-WIN55,212-2, and antagonist/inverse agonists of cannabinoid receptors, AM251, and cannabidiol were examined in pig brain mitochondria. Different effects of these cannabinoids on mitochondrial respiratory chain complexes and citrate synthase were found. Citrate synthase activity was decreased only by Δ(9)-tetrahydrocannabinol and AM251. Significant increase in the complex I activity was induced by anandamide. At micromolar concentration, all the tested cannabinoids inhibited the activity of electron transport chain complexes II/III and IV. Stimulatory effect of anandamide on activity of complex I may participate on distinct physiological effects of endocannabinoids compared to phytocannabinoids or synthetic cannabinoids. Common inhibitory effect of cannabinoids on activity of complex II/III and IV confirmed a non-receptor-mediated mechanism of cannabinoid action on individual components of system of oxidative phosphorylation.

摘要

本研究的目的是调查药理学上不同的大麻素所诱导的单个线粒体呼吸链复合物(I、II/III、IV)和柠檬酸合酶活性的变化。在从猪脑分离的粗线粒体组分中测定了所选大麻素对线粒体酶的体外作用。在猪脑线粒体中检测了大麻素受体激动剂Δ(9)-四氢大麻酚、花生四烯乙醇胺和R-(+)-WIN55,212-2,以及大麻素受体拮抗剂/反向激动剂AM251和大麻二酚。发现这些大麻素对线粒体呼吸链复合物和柠檬酸合酶有不同的作用。仅Δ(9)-四氢大麻酚和AM251降低了柠檬酸合酶活性。花生四烯乙醇胺诱导复合物I活性显著增加。在微摩尔浓度下,所有测试的大麻素均抑制电子传递链复合物II/III和IV的活性。与植物大麻素或合成大麻素相比,花生四烯乙醇胺对复合物I活性的刺激作用可能参与了内源性大麻素的不同生理效应。大麻素对复合物II/III和IV活性的共同抑制作用证实了大麻素对氧化磷酸化系统各个组分的作用存在非受体介导机制。

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