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体内用诱变致癌杂环胺对核酸进行修饰。从注射了3-氨基-1-甲基-5H-吡啶并[4,3-b]吲哚和2-氨基-6-甲基二吡啶并[1,2-a:3',2'-d]咪唑的大鼠中提取的DNA中修饰碱基的鉴定。

Modification of nucleic acids with muta-carcinogenic heteroaromatic amines in vivo. Identification of modified bases in DNA extracted from rats injected with 3-amino-1-methyl-5H-pyrido[4,3-b]indole and 2-amino-6-methyldipyrido[1,2-a3:3',2'-d]imidazole.

作者信息

Hashimoto Y, Shudo K, Okamoto T

出版信息

Mutat Res. 1982 Aug;105(1-2):9-13. doi: 10.1016/0165-7992(82)90200-7.

Abstract

Potent muta-carcinogens isolated from amino-acid pyrolysates, 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2) and 2-amino-1-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1), were injected intraperitoneally into Male Wistar rats. DNA and rRNA modified with these muta-carcinogens were then extracted from the livers of the rats, and modified nucleic-acid bases were isolated and analysed by high-performance liquid chromatography (HPLC). These modified nucleic-acid bases were identified as 3-(C8-guanyl)amino-1-methyl-5H-pyrido[4,3-b]indole (Gua-Trp-P-2) and 2-(C8-guanyl)amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Gua-Glu-P-1) by comparison of their retention times on HPLC and UV spectra with those of authentic compounds.

摘要

从氨基酸热解产物中分离出的强效诱变致癌物3-氨基-1-甲基-5H-吡啶并[4,3-b]吲哚(Trp-P-2)和2-氨基-1-甲基二吡啶并[1,2-a:3',2'-d]咪唑(Glu-P-1),经腹腔注射到雄性Wistar大鼠体内。然后从大鼠肝脏中提取用这些诱变致癌物修饰的DNA和rRNA,并通过高效液相色谱法(HPLC)分离和分析修饰的核酸碱基。通过比较它们在HPLC上的保留时间和紫外光谱与标准化合物的保留时间和紫外光谱,将这些修饰的核酸碱基鉴定为3-(C8-鸟嘌呤基)氨基-1-甲基-5H-吡啶并[4,3-b]吲哚(Gua-Trp-P-2)和2-(C8-鸟嘌呤基)氨基-6-甲基二吡啶并[1,2-a:3',2'-d]咪唑(Gua-Glu-P-1)。

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