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大鼠肝脏和人肝脏药物代谢酶的死后变化

Post mortem changes in drug-metabolizing enzymes of rat liver and human liver.

作者信息

Gallenkamp H, Berger C, Buschmann J, Richter E

出版信息

Hepatogastroenterology. 1981 Dec;28(6):308-10.

PMID:6284626
Abstract

The aim of this investigation was to obtain information on the time-dependent decrease of the drug-metabolizing system in autolysing rat liver, and also in human cadaver liver. Rat liver, divided into three parts, was tested immediately after removal and 6 and 12 hrs later. Parameters investigated were: microsomal protein, cytochrome P-450, NADPH cytochrome C reductase, glucose-6-phosphatase, aminopyrine-N-demethylation and aniline-p-hydroxylation. In human liver, samples taken from 0.5 up to 3.5 hrs after death, microsomal protein cytochrome P-450, NADPH cytochrome C reductase and phospholipids were tested. Nearly all parameters based on microsomal protein decrease during autolysis, but by different amounts. Interestingly, the cytochrome P-450 content of patients with signs of shock 12 hrs before death is significantly lower than in patients without shock.

摘要

本研究的目的是获取有关自溶大鼠肝脏以及人尸体肝脏中药物代谢系统随时间下降的信息。大鼠肝脏被分成三部分,在取出后立即、6小时后和12小时后进行检测。所研究的参数包括:微粒体蛋白、细胞色素P - 450、NADPH细胞色素C还原酶、葡萄糖 - 6 - 磷酸酶、氨基比林 - N - 脱甲基化和苯胺 - p - 羟基化。对于人肝脏,在死后0.5至3.5小时采集的样本,检测了微粒体蛋白、细胞色素P - 450、NADPH细胞色素C还原酶和磷脂。几乎所有基于微粒体蛋白的参数在自溶过程中都会下降,但下降幅度不同。有趣的是,死亡前12小时出现休克迹象的患者,其细胞色素P - 450含量显著低于无休克的患者。

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