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短期和长期乙醇处理及酒精戒断对大鼠肝细胞磷脂生物合成影响的比较研究。

Comparative study of the effects of short- and long-term ethanol treatment and alcohol withdrawal on phospholipid biosynthesis in rat hepatocytes.

作者信息

Carrasco M P, Jiménez-López J M, Segovia J L, Marco C

机构信息

Department of Biochemistry and Molecular Biology, Faculty of Sciences, University of Granada, 18001, Granada, Spain.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2002 Mar;131(3):491-7. doi: 10.1016/s1096-4959(02)00006-4.

Abstract

This study describes the effects of short- and long-term ethanol treatment and withdrawal on the biosynthesis of the phospholipids phosphatidylcholine (PC) and phosphatidylethanolamine (PE) in hepatocytes isolated from rats, using isotopically labelled choline and ethanolamine as exogenous precursors. Our results demonstrate that short-term ethanol consumption increases the incorporation of exogenous polar bases into PC and PE, whereas long-term ethanol administration provokes a differential effect in both PC and PE biosynthesis via cytidine diphosphate derivatives (CDP-derivatives), decreasing PC synthesis and increasing the biosynthesis of PE. We suggest that the increased biosynthesis of PE after ethanol treatment results from changes in lipogenic substrates produced as a consequence of ethanol metabolism, whilst the specific inhibition of PC biosynthesis seems to be a consequence of alterations of enzymes involved in the CDP-choline pathway. With regard to the influence of ethanol on PE methylation to give PC, our results demonstrate that ethanol activates this pathway in short-term, as well as chronic ethanol treatment. Ethanol withdrawal returns the activity of the PC and PE pathways to control levels. The alterations in the biosynthesis of the main phospholipids, PC and PE, demonstrated in this study could be of a great physiological interest in determining the pathology of alcoholism.

摘要

本研究描述了短期和长期乙醇处理及戒断对从大鼠分离的肝细胞中磷脂酰胆碱(PC)和磷脂酰乙醇胺(PE)生物合成的影响,使用同位素标记的胆碱和乙醇胺作为外源性前体。我们的结果表明,短期摄入乙醇会增加外源性极性碱基掺入PC和PE,而长期给予乙醇会通过胞苷二磷酸衍生物(CDP-衍生物)对PC和PE生物合成产生不同影响,降低PC合成并增加PE的生物合成。我们认为,乙醇处理后PE生物合成增加是由于乙醇代谢产生的生脂底物变化所致,而PC生物合成的特异性抑制似乎是CDP-胆碱途径中相关酶改变的结果。关于乙醇对PE甲基化生成PC的影响,我们的结果表明,乙醇在短期以及慢性乙醇处理中都会激活该途径。乙醇戒断使PC和PE途径的活性恢复到对照水平。本研究中证明的主要磷脂PC和PE生物合成的改变,在确定酒精中毒病理学方面可能具有重大的生理学意义。

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