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长期给大鼠喂食乙醇对肝脏线粒体膜结构和功能的影响。

The influence of chronic ethanol feeding to rats on liver mitochondrial membrane structure and function.

作者信息

Hosein E A, Lee H, Hofmann I

出版信息

Can J Biochem. 1980 Oct;58(10):1147-55. doi: 10.1139/o80-154.

DOI:10.1139/o80-154
PMID:6257339
Abstract

Arrhenius plots were generated on the activity of rat liver mitochondrial cytochrome c oxidase from Metrecal-sucrose fed controls and Metrecal-alcohol fed experimentals. Chronic alcohol feeding resulted in diminished specific activity of cytochrome c oxidase and abolition of the discontinuity temperature at 17.5 degrees C found in the controls. Twenty-four hours after alcohol withdrawal, a discontinuity temperature reappeared at 14.4 degrees C; at 48 h it increased to 22.6 degrees C and returned to normal (17.4 degrees C) at 72 h. Such liver mitochondria also showed a decreased capacity to oxidize the acetyl group of acetyl carnitine immediately following prolonged alcohol feeding. When the assay was performed following withdrawal from alcohol 24 h later, oxidation was enhanced and this effect persisted for another 48 h. These latter results revealed a diminished capacity of such mitochondria to oxidize short chain fatty acids during alcohol feeding and the reverse during alcohol withdrawal. These results, complemented by thermographic data obtained through differential scanning calorimetry (DSC) reinforced the view that chronic alcoholic feeding induced adaptive changes in the fluidity of rat liver mitochondrial membrane lipids. Moreover, they demonstrated that in the microenvironment of the membrane-bound enzymes on withdrawal from ethanol, the membrane readapts to the new conditions without alcohol. This involved modulation of membrane structure and function and at the same time demonstrated a role for the membrane in the expression of tolerance and functional dependence on alcohol.

摘要

绘制了食用美特餐 - 蔗糖的对照组和食用美特餐 - 酒精的实验组大鼠肝脏线粒体细胞色素c氧化酶活性的阿累尼乌斯图。长期饮酒导致细胞色素c氧化酶的比活性降低,且消除了对照组中在17.5摄氏度时出现的不连续温度。戒酒24小时后,14.4摄氏度时重新出现不连续温度;48小时时升高至22.6摄氏度,并在72小时时恢复正常(17.4摄氏度)。长期饮酒后,此类肝脏线粒体氧化乙酰肉碱乙酰基的能力也立即下降。在24小时后戒酒再进行测定时,氧化作用增强,且这种作用持续另外48小时。后一组结果表明,此类线粒体在饮酒期间氧化短链脂肪酸的能力下降,而在戒酒期间则相反。这些结果,再加上通过差示扫描量热法(DSC)获得的热成像数据,强化了长期酒精喂养诱导大鼠肝脏线粒体膜脂流动性适应性变化的观点。此外,它们表明,在从乙醇中撤出后膜结合酶的微环境中,膜重新适应无酒精的新条件。这涉及膜结构和功能的调节,同时证明了膜在酒精耐受性表达和功能依赖性中的作用。

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引用本文的文献

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Ethanol withdrawal provokes opening of the mitochondrial membrane permeability transition pore in an estrogen-preventable manner.乙醇戒断以雌激素可预防的方式引发线粒体膜通透性转换孔的开放。
J Pharmacol Exp Ther. 2009 Mar;328(3):692-8. doi: 10.1124/jpet.108.146829. Epub 2008 Dec 2.
2
Ethanol withdrawal provokes mitochondrial injury in an estrogen preventable manner.乙醇戒断以一种雌激素可预防的方式引发线粒体损伤。
J Bioenerg Biomembr. 2008 Feb;40(1):35-44. doi: 10.1007/s10863-008-9129-y. Epub 2008 Jan 19.
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Ethanol withdrawal posttranslationally decreases the activity of cytochrome c oxidase in an estrogen reversible manner.
乙醇戒断在翻译后以雌激素可逆的方式降低细胞色素c氧化酶的活性。
Neurosci Lett. 2007 Apr 12;416(2):160-4. doi: 10.1016/j.neulet.2007.01.065. Epub 2007 Feb 2.
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Secretion of high density lipoprotein by the isolated perfused alcoholic rat liver.酒精性大鼠离体灌注肝脏中高密度脂蛋白的分泌
Experientia. 1982 Aug 15;38(8):914-5. doi: 10.1007/BF01953650.