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起始tRNA接受试验作为致癌物的短期检测方法。1. 标准化程序。

The initiator tRNA acceptance assay as a short-term test for carcinogens. 1. A standardized procedure.

作者信息

Hradec J

机构信息

Department of Molecular Biology, Research Institute for Tuberculosis and Respiratory Diseases, Prague, Czechoslovakia.

出版信息

Carcinogenesis. 1988 May;9(5):837-42. doi: 10.1093/carcin/9.5.837.

Abstract

A short-term test for carcinogens has been developed based on the interaction of chemical carcinogens with tRNA(FMet) in vitro. Transfer RNA from rat or rabbit liver is pre-treated with compounds to be tested in the presence of microsomal enzymes and NADPH. Re-isolated tRNA is then charged with L-methionine by aminoacyl-tRNA synthetases from E. coli B. Carcinogens induce a stimulation of tRNA charging whereas chemically similar non-carcinogenic compounds do not show this effect. Experiments with model substances N-methyl-N'-nitro-N-nitrosoguanidine (strong carcinogen) and aflatoxin G1 (weak carcinogen) revealed some differences in dose effect relationships. It is advisable to test unknown compounds at three different concentrations (10(-5), 10(-7) and 10(-9) mg/ml) with at least two different quantities of microsomal enzymes. Tests on greater than 150 different compounds performed so far indicate that the evaluation of results as % of stimulation (when compared with the control value obtained with the charging of tRNA treated with the solvent only) may allow a quantitative discrimination between weak and intermediate, and strong carcinogens. The procedure is rapid, well reproducible and relatively inexpensive and may be used to complement the other short-term tests for carcinogenicity.

摘要

基于化学致癌物与体外甲硫氨酸起始转运核糖核酸(tRNA(FMet))的相互作用,已开发出一种致癌物短期检测方法。来自大鼠或兔肝脏的转运核糖核酸在微粒体酶和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)存在的情况下,用待检测的化合物进行预处理。然后,通过大肠杆菌B的氨酰基转运核糖核酸合成酶,将再分离的转运核糖核酸与L-甲硫氨酸结合。致癌物会刺激转运核糖核酸的结合,而化学结构相似的非致癌化合物则不会出现这种效应。用模型物质N-甲基-N'-硝基-N-亚硝基胍(强致癌物)和黄曲霉毒素G1(弱致癌物)进行的实验揭示了剂量效应关系上的一些差异。建议用至少两种不同量的微粒体酶,在三种不同浓度(10(-5)、10(-7)和10(-9)毫克/毫升)下检测未知化合物。迄今为止,对150多种不同化合物进行的检测表明,将结果评估为刺激百分比(与仅用溶剂处理转运核糖核酸结合时获得的对照值相比),可能有助于对弱致癌物、中度致癌物和强致癌物进行定量区分。该方法快速、可重复性好且相对便宜,可用于补充其他致癌性短期检测方法。

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