大鼠给予苯巴比妥后肝脏磷脂酰胆碱生物合成途径的评价:磷脂酰胆碱分子种类的研究。

G C Ram, U K Misra
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引用次数: 0

摘要

雌性大鼠给予苯巴比妥显著提高肝脏单、二、四烯PC水平,血浆磷脂酰胆碱及其单、二烯类升高,甘油三酯水平降低。在苯巴比妥治疗的大鼠中,NaH2 32PO4掺入单核细胞和二单核细胞的数量明显减少。苯巴比妥显著增加14ch3 -蛋氨酸在肝脏四烯体和六烯体PC中的掺入。与对照组相比,苯巴比妥治疗大鼠血浆中NaH2 32PO4掺入单、二烯体PC不受影响,而14ch3 -蛋氨酸掺入四、六烯体PC受到抑制。苯巴比妥通过n -甲基化PE促进PC合成,并通过cdp -胆碱途径抑制PC合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of biosynthetic pathways of phosphatidyl choline in liver of rats given phenobarbital: a study on molecular species of phosphatidyl choline.

Administration of phenobarbital to female rats significantly increased the levels of liver monoenoic, dienoic and tetraenoic PC and in plasma it raised phosphatidyl choline and its monoenoic and dienoic species and decreased triglyceride levels. Significant reductions in the incorporation of NaH2 32PO4 into monoenoic and dienoic PC were observed in phenobarbital treated rats. Phenobarbital administration significantly increased the incorporation of 14CH3-methionine into tetraenoic and hexaenoic PC of liver. In plasma the incorporation of NaH2 32PO4 into monoenoic and dienoic PC in phenobarbital treated rats was not affected but that of 14CH3-methionine incorporation into tetraenoic and hexaenoic PC was suppressed as compared to the control. Phenobarbital enhanced PC synthesis Via N-methylation of PE and depressed via CDP-choline pathway.

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