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小剂量二甲基亚硝胺作用后大鼠肝脏和肾脏中脱氧核糖核酸O6-甲基鸟嘌呤的形成及随后的去除

Formation and subsequent removal of O6-methylguanine from deoxyribonucleic acid in rat liver and kidney after small doses of dimethylnitrosamine.

作者信息

Pegg A E, Hui G

出版信息

Biochem J. 1978 Sep 1;173(3):739-48. doi: 10.1042/bj1730739.

Abstract
  1. The amounts of 7-methylguanine and O(6)-methylguanine present in the DNA of liver and kidney of rats 4h and 24h after administration of low doses of dimethylnitrosamine were measured. 2. O(6)-Methylguanine was rapidly removed from liver DNA so that less than 15% of the expected amount (on the basis of 7-methylguanine found) was present within 4h after doses of 0.25mg/kg body wt. or less. Within 24h of administration of dimethylnitrosamine at doses of 1mg/kg or below, more than 85% of the expected amount of O(6)-methylguanine was removed. Removal was most efficient (defined in terms of the percentage of the O(6)-methylguanine formed that was subsequently lost within 24h) after doses of 0.25-0.5mg/kg body wt. At doses greater or less than this the removal was less efficient, even though the absolute amount of O(6)-methylguanine lost during 24h increased with the dose of dimethylnitrosamine over the entire range of doses from 0.001 to 20mg/kg body wt. 3. Alkylation of kidney DNA after intraperitoneal injections of 1-50mug of dimethylnitrosamine/kg body wt. occurred at about one-tenth the extent of alkylation of liver DNA. Removal of O(6)-methylguanine from the DNA also took place in the kidney, but was slower than in the liver. 4. After oral administration of these doses of dimethylnitrosamine, the alkylation of kidney DNA was much less than after intraperitoneal administration and represented only 1-2% of that found in the liver. 5. Alkylation of liver and kidney DNA was readily detectable when measured 24h after the final injection in rats that received daily injections of 1mug of [(3)H]dimethylnitrosamine/kg for 2 or 3 weeks. After 3 weeks, O(6)-methylguanine contents in the liver DNA were about 1% of the 7-methylguanine contents. The amount of 7-methylguanine in the liver DNA was 10 times that in the kidney DNA, but liver O(6)-methylguanine contents were only twice those in the kidney. 6. Extracts able to catalyse the removal of O(6)-methylguanine from alkylated DNA in vitro were isolated from liver and kidney. These extracts did not lead to the loss of 7-methylguanine from DNA. 7. The possible relevance of the formation and removal of O(6)-methylguanine in DNA to the risk of tumour induction by exposure to low concentrations of dimethylnitrosamine is discussed.
摘要
  1. 测定了低剂量二甲基亚硝胺给药后4小时和24小时大鼠肝脏和肾脏DNA中7-甲基鸟嘌呤和O(6)-甲基鸟嘌呤的含量。2. O(6)-甲基鸟嘌呤从肝脏DNA中迅速去除,因此在给予0.25mg/kg体重或更低剂量后4小时内,其含量低于预期量(基于所发现的7-甲基鸟嘌呤)的15%。在给予1mg/kg或更低剂量的二甲基亚硝胺后24小时内,超过85%的预期量的O(6)-甲基鸟嘌呤被去除。在给予0.25 - 0.5mg/kg体重剂量后,去除效率最高(以形成的O(6)-甲基鸟嘌呤在随后24小时内损失的百分比来定义)。在此剂量之上或之下,去除效率较低,尽管在24小时内损失的O(6)-甲基鸟嘌呤的绝对量随着二甲基亚硝胺剂量在0.001至20mg/kg体重的整个范围内增加。3. 腹腔注射1 - 50μg二甲基亚硝胺/kg体重后,肾脏DNA的烷基化程度约为肝脏DNA烷基化程度的十分之一。O(6)-甲基鸟嘌呤也从肾脏DNA中去除,但比在肝脏中慢。4. 口服这些剂量的二甲基亚硝胺后,肾脏DNA的烷基化程度远低于腹腔注射后,仅占肝脏中所发现的烷基化程度的1 - 2%。5. 在每天注射1μg[(3)H]二甲基亚硝胺/kg体重持续2或3周的大鼠中,在最后一次注射后24小时测量时,肝脏和肾脏DNA的烷基化很容易检测到。3周后,肝脏DNA中O(6)-甲基鸟嘌呤的含量约为7-甲基鸟嘌呤含量的1%。肝脏DNA中7-甲基鸟嘌呤的含量是肾脏DNA中7-甲基鸟嘌呤含量的10倍,但肝脏中O(6)-甲基鸟嘌呤的含量仅是肾脏中的两倍。6. 从肝脏和肾脏中分离出了能够在体外催化从烷基化DNA中去除O(6)-甲基鸟嘌呤的提取物。这些提取物不会导致DNA中7-甲基鸟嘌呤的损失。7. 讨论了DNA中O(6)-甲基鸟嘌呤的形成和去除与低浓度二甲基亚硝胺暴露导致肿瘤诱导风险的可能相关性。

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本文引用的文献

1
N-nitroso compounds: detection in ambient air.亚硝胺类化合物:环境空气中的检测。
Science. 1976 Jun 25;192(4246):1328-30. doi: 10.1126/science.192.4246.1328.
8
Nitrosamines as environmental carcinogens.亚硝胺作为环境致癌物。
Nature. 1970 Jan 3;225(5227):21-3. doi: 10.1038/225021a0.

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