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硫唑嘌呤与谷胱甘肽在大鼠肝脏中的相互作用。

Interaction of azathioprine and glutathione in the liver of the rat.

作者信息

Kaplowitz N

出版信息

J Pharmacol Exp Ther. 1977 Mar;200(3):479-86.

PMID:850124
Abstract

Azathioprine was administered to rats in order to study its interaction with glutathione in vivo. Glutathione levels were measured sequentially in liver, red blood cells, kidney and small intestine after i.p. injections of azathioprine (6.25-100 micronmol/100 g b.wt.). Five minutes after drug administration, dose-related selective depletion of hepatic glutathione up to 50% of control was observed. By 60 minutes 80% depletion of hepatic glutathione was observed. Red cell glutathione depletion was also observed but lagged behind hepatic changes. Five minutes after azathioprine administrations, no change in red cell glutathione was seen with all doses of azathioprine, but a dose-related increase in plasma 6-mercaptopurine and azathioprine was observed. At all azathioprine doses and at all time intervals after drug administration, the hepatic contribution to total glutathione consumption predominated. No change in glutathione levels in kidney or small intestine was observed after azathioprine. Thus, the liver plays a major role in the metabolism of azathioprine through the interaction of the drug with glutathione.

摘要

为了研究硫唑嘌呤在体内与谷胱甘肽的相互作用,将其给予大鼠。腹腔注射硫唑嘌呤(6.25 - 100微摩尔/100克体重)后,依次测量肝脏、红细胞、肾脏和小肠中的谷胱甘肽水平。给药5分钟后,观察到肝脏谷胱甘肽出现与剂量相关的选择性消耗,最高可达对照值的50%。到60分钟时,观察到肝脏谷胱甘肽消耗了80%。红细胞谷胱甘肽也出现消耗,但滞后于肝脏的变化。硫唑嘌呤给药5分钟后,所有剂量的硫唑嘌呤均未引起红细胞谷胱甘肽的变化,但观察到血浆6 - 巯基嘌呤和硫唑嘌呤与剂量相关的增加。在所有硫唑嘌呤剂量及给药后的所有时间间隔,肝脏对总谷胱甘肽消耗的贡献占主导。硫唑嘌呤给药后,肾脏或小肠中的谷胱甘肽水平未观察到变化。因此,肝脏通过药物与谷胱甘肽的相互作用在硫唑嘌呤的代谢中起主要作用。

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