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与正常肝脏相比,致癌物诱导的肝细胞结节中2-乙酰氨基芴的代谢模式。

The pattern of metabolism of 2-acetylaminofluorene in carcinogen-induced hepatocyte nodules in comparison to normal liver.

作者信息

Spiewak Rinaudo J A, Farber E

出版信息

Carcinogenesis. 1986 Apr;7(4):523-8. doi: 10.1093/carcin/7.4.523.

Abstract

This study was designed to test further the hypothesis that the special biochemical pattern seen in hepatocyte nodules during liver carcinogenesis could be of fundamental importance in their selective metabolism of one carcinogenic xenobiotic, 2-AAF, as related to their resistance to xenobiotics. Nodules of a certain stage were induced using the resistant hepatocyte model. The metabolism of a single small dose of 2-AAF in hepatocyte nodules in comparison to normal liver was studied at different time intervals up to 30 h. The levels of free 2-AAF in nodules and in normal liver were approximately the same over the whole time period. However, the nodules showed a large decrease in the binding of 2-AAF to DNA, RNA and proteins as well as in the metabolic conversion to hydroxylated forms, both free and conjugated with glucuronic acid. The patterns of metabolic conversion to metabolites and of conjugation of the metabolites are in harmony with the known biochemical patterns in nodules, a decrease in phase I components involved in the metabolism of carcinogens and other xenobiotics and an increase in most phase II components involved in conjugation and detoxification.

摘要

本研究旨在进一步验证以下假说

在肝癌发生过程中,肝细胞结节中所见的特殊生化模式,对于其对一种致癌性异生物2-氨基芴(2-AAF)的选择性代谢可能至关重要,这与它们对异生物的抗性相关。使用抗性肝细胞模型诱导出特定阶段的结节。在长达30小时的不同时间间隔内,研究了与正常肝脏相比,单个小剂量2-AAF在肝细胞结节中的代谢情况。在整个时间段内,结节和正常肝脏中游离2-AAF的水平大致相同。然而,结节中2-AAF与DNA、RNA和蛋白质的结合以及代谢转化为羟基化形式(包括游离的和与葡萄糖醛酸结合的)均大幅下降。代谢转化为代谢产物的模式以及代谢产物的结合模式与结节中已知的生化模式一致,即参与致癌物和其他异生物代谢的I相成分减少,而参与结合和解毒的大多数II相成分增加。

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