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谷胱甘肽耗竭诱导离体小鼠肝细胞中依赖糖原分解的抗坏血酸合成。

Glutathione depletion induces glycogenolysis dependent ascorbate synthesis in isolated murine hepatocytes.

作者信息

Braun L, Csala M, Poussu A, Garzó T, Mandl J, Bánhegyi G

机构信息

Department of Medical Chemistry, Semmelweis University of Medicine, Budapest, Hungary.

出版信息

FEBS Lett. 1996 Jun 17;388(2-3):173-6. doi: 10.1016/0014-5793(96)00548-0.

Abstract

The relationship between glutathione deficiency, glycogen metabolism and ascorbate synthesis was investigated in isolated murine hepatocytes. Glutathione deficiency caused by various agents increased ascorbate synthesis with a stimulation of glycogen breakdown. Increased ascorbate synthesis from UDP-glucose or gulonolactone could not be further affected by glutathione depletion. Fructose prevented the stimulated glycogenolysis and ascorbate synthesis caused by glutathione consumption. Reduction of oxidised glutathione by dithiothreitol decreased the elevated glycogenolysis and ascorbate synthesis in diamide or menadione treated hepatocytes. Our results suggest that a change in GSH/GSSG ratio seems to be a sufficient precondition of altering glycogenolysis and a consequent ascorbate synthesis.

摘要

在分离的小鼠肝细胞中研究了谷胱甘肽缺乏、糖原代谢和抗坏血酸合成之间的关系。各种试剂引起的谷胱甘肽缺乏会增加抗坏血酸的合成,并刺激糖原分解。UDP-葡萄糖或古洛糖酸内酯引起的抗坏血酸合成增加不会因谷胱甘肽耗竭而进一步受到影响。果糖可防止谷胱甘肽消耗引起的糖原分解和抗坏血酸合成增加。二硫苏糖醇将氧化型谷胱甘肽还原,降低了二酰胺或甲萘醌处理的肝细胞中升高的糖原分解和抗坏血酸合成。我们的结果表明,GSH/GSSG比值的变化似乎是改变糖原分解以及随之而来的抗坏血酸合成的充分前提条件。

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