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Methylation of liver DNA guanine in hydrazine hepatotoxicity: dose-response and kinetic characteristics of 7-methylguanine and O6-methylguanine formation and persistence in rats.

作者信息

Becker R A, Barrows L R, Shank R C

出版信息

Carcinogenesis. 1981;2(11):1181-8. doi: 10.1093/carcin/2.11.1181.

DOI:10.1093/carcin/2.11.1181
PMID:7318155
Abstract

Fischer 344 or Sprague Dawley rats were fasted overnight and given orally 30--90 mg hydrazine/kg body wt. The presence of 7-methylguanine and O6-methylguanine in liver DNA was demonstrated 5 and 24 h after hydrazine administration using two different analytical techniques. Methylation levels changed little with dose except for the highest dose (ca. LD50) at which the levels doubled. In a time-response study, rats were given 90 mg hydrazine/kg body wt. and killed 0.25 to 96 h later. Both 7-methylguanine and O6-methylguanine were detected quantitatively in liver DNA from rats as early as 15 min after hydrazine administration. After maximum levels of methylguanines had formed, 7-methylguanine was removed from DNA at a rate of approximately 50% in 47 h; the half-life of O6-methylguanine in liver DNA was approximately 13 hr. Three or four, but not one or two, daily administrations of 3 mg hydrazine/kg body wt. also produced detectable levels of 7-methylguanine in rat liver DNA. Neither 7-methylguanine or O6-methylguanine was detected in comparable amounts of liver DNA from control animals. The study confirms the observation that hydrazine administration results in the formation of methylated guanines in liver DNA.

摘要

相似文献

1
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引用本文的文献

1
Nonenzymatic methylation of DNA by the intracellular methyl group donor S-adenosyl-L-methionine is a potentially mutagenic reaction.细胞内甲基供体S-腺苷-L-甲硫氨酸对DNA的非酶促甲基化是一种潜在的诱变反应。
EMBO J. 1982;1(2):211-6. doi: 10.1002/j.1460-2075.1982.tb01149.x.
2
O6-methylguanine repair in liver cells in vivo: comparison between G1- and S-phase of the cell cycle.体内肝细胞中的O6-甲基鸟嘌呤修复:细胞周期G1期和S期之间的比较
J Cancer Res Clin Oncol. 1984;108(1):36-45. doi: 10.1007/BF00390971.
3
Nucleic acid adducts of chemical carcinogens and mutagens.
化学致癌物和诱变剂的核酸加合物
Arch Toxicol. 1983 Apr;52(4):249-85. doi: 10.1007/BF00316495.
4
Cell cycle-dependent intervention by benzamide of carcinogen-induced neoplastic transformation and in vitro poly(ADP-ribosyl)ation of nuclear proteins in human fibroblasts.苯甲酰胺对致癌物诱导的人成纤维细胞肿瘤转化及核蛋白体外多聚(ADP-核糖基)化的细胞周期依赖性干预。
Proc Natl Acad Sci U S A. 1983 Dec;80(23):7219-23. doi: 10.1073/pnas.80.23.7219.
5
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J Cancer Res Clin Oncol. 1986;112(3):189-95. doi: 10.1007/BF00395911.