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儿茶酚胺和MPP(+)对脑线粒体膜通透性及PC12细胞活力的差异作用。

Differential effect of catecholamines and MPP(+) on membrane permeability in brain mitochondria and cell viability in PC12 cells.

作者信息

Lee Chung Soo, Han Jeong Ho, Jang Yoon Young, Song Jin Ho, Han Eun Sook

机构信息

Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul 156-756, South Korea.

出版信息

Neurochem Int. 2002 Apr;40(4):361-9. doi: 10.1016/s0197-0186(01)00069-9.

Abstract

The present study examined the effect of dopamine, 6-hydroxydopamine (6-OHDA), and MPP(+) on the membrane permeability transition in brain mitochondria and on viability in PC12 cells. Dopamine and 6-hydroxydopamine induced the swelling and membrane potential change in mitochondria, which was inhibited by addition of antioxidant enzymes, SOD and catalase. In contrast, antioxidant enzymes did not reduce the effect of MPP(+) on mitochondrial swelling and membrane potential. Catecholamines enhanced the Ca(2+) uptake and release by mitochondria, and the addition of MPP(+) induced Ca(2+) release. Catecholamines induced a thiol oxidation in mitochondria that was decreased by antioxidant enzymes. MPP(+) showed a little effect on the cytochrome c release from mitochondria and did not induce thiol oxidation. Catecholamines and MPP(+) induced a cell death, including apoptosis, in PC12 cells that was inhibited by addition of antioxidant enzymes. The result suggests that the oxidation of dopamine and 6-hydroxydopamine could modulate the membrane permeability in brain mitochondria and induce PC12 cell death, which may be ascribed to oxidative stress. MPP(+) appears to exert a toxic effect on neuronal cells by the action, which is different from catecholamines.

摘要

本研究考察了多巴胺、6-羟基多巴胺(6-OHDA)和1-甲基-4-苯基吡啶离子(MPP(+))对脑线粒体膜通透性转换及PC12细胞活力的影响。多巴胺和6-羟基多巴胺可诱导线粒体肿胀及膜电位变化,添加抗氧化酶超氧化物歧化酶(SOD)和过氧化氢酶可抑制该变化。相比之下,抗氧化酶不能降低MPP(+)对线粒体肿胀及膜电位的影响。儿茶酚胺可增强线粒体对钙离子的摄取和释放,添加MPP(+)可诱导钙离子释放。儿茶酚胺可诱导线粒体内的硫醇氧化,抗氧化酶可使其降低。MPP(+)对线粒体细胞色素c释放影响较小,且不诱导硫醇氧化。儿茶酚胺和MPP(+)可诱导PC12细胞死亡,包括凋亡,添加抗氧化酶可抑制该过程。结果表明,多巴胺和6-羟基多巴胺的氧化可调节脑线粒体膜通透性并诱导PC12细胞死亡,这可能归因于氧化应激。MPP(+)似乎通过与儿茶酚胺不同的作用机制对神经元细胞产生毒性作用。

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