• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

The mechanism of cocarcinogenic action of ethanol in rat liver.

作者信息

Schwarz M, Buchmann A, Moore M, Kunz W

出版信息

IARC Sci Publ. 1984(56):83-90.

PMID:6536612
Abstract

The effects of chronic alcohol consumption on nitrosamine metabolism in vivo, DNA synthesis and repair, and carcinogen-induced preneoplasia were studied in rat liver. Following a single injection of different doses of 14C-N-nitrosodimethylamine, there was no significant difference between controls and ethanol-pretreated rats in the alkylation pattern of cellular protein nor in the levels of the alkylation products 7-methylguanine and O6-methylguanine isolated from liver DNA. O6-Methylguanine-specific DNA repair was also unchanged. An increase in the number and size of foci staining negative for adenosine triphosphatase and/or positive for gamma-glutamyltranspeptidase was observed in rats treated intermittently with ethanol and N-nitrosomorpholine. The numbers of clear-cell and mixed-cell foci were also increased. An ethanol-mediated enhancement of DNA synthesis, which was ascertained by different methods, may be related to this cocarcinogenic action of the alcohol. Ethanol, however, failed to demonstrate promoting activity. Long-term treatment of carcinogen pretreated rats with ethanol, according to the classical initiation-promotion protocol, had no effect on the incidence of preneoplastic foci in liver.

摘要

相似文献

1
The mechanism of cocarcinogenic action of ethanol in rat liver.
IARC Sci Publ. 1984(56):83-90.
2
Alkylation of DNA and tissue specificity in nitrosamine carcinogenesis.亚硝胺致癌作用中DNA的烷基化与组织特异性
J Supramol Struct Cell Biochem. 1981;17(3):259-73. doi: 10.1002/jsscb.380170307.
3
DNA synthesis, apoptosis, and phenotypic expression as determinants of growth of altered foci in rat liver during phenobarbital promotion.在苯巴比妥促进作用下,DNA合成、细胞凋亡及表型表达作为大鼠肝脏中改变灶生长的决定因素。
Cancer Res. 1990 Aug 15;50(16):5127-35.
4
Stability and capacity of dimethylnitrosamine-induced O6-methylguanine repair system in rat liver.二甲基亚硝胺诱导的大鼠肝脏O6-甲基鸟嘌呤修复系统的稳定性和容量
Cancer Res. 1983 Dec;43(12 Pt 1):5808-14.
5
Effect of phenobarbital and other liver monooxygenase modifiers on dimethylnitrosamine-induced alkylation of rat liver macromolecules.苯巴比妥及其他肝脏单加氧酶调节剂对二甲基亚硝胺诱导的大鼠肝脏大分子烷基化作用的影响。
Cancer Res. 1985 May;45(5):2020-4.
6
Modulation of repair of O6-methylguanine in parenchymal and nonparenchymal liver cells of rats treated with dimethylnitrosamine.二甲基亚硝胺处理大鼠的实质和非实质肝细胞中O6-甲基鸟嘌呤修复的调节
Cancer Res. 1985 Oct;45(10):4768-73.
7
Final report on the safety assessment of capsicum annuum extract, capsicum annuum fruit extract, capsicum annuum resin, capsicum annuum fruit powder, capsicum frutescens fruit, capsicum frutescens fruit extract, capsicum frutescens resin, and capsaicin.关于辣椒提取物、辣椒果实提取物、辣椒树脂、辣椒果粉、小米辣果实、小米辣果实提取物、小米辣树脂和辣椒素安全性评估的最终报告。
Int J Toxicol. 2007;26 Suppl 1:3-106. doi: 10.1080/10915810601163939.
8
Effect of acute doses of 2-acetylaminofluorene on the capacity of rat liver to repair methylated purines in DNA in vivo and in vitro.急性剂量的2-乙酰氨基芴对大鼠肝脏在体内和体外修复DNA中甲基化嘌呤能力的影响。
Cancer Res. 1982 Oct;42(10):4203-9.
9
Promotion of spontaneous preneoplastic cells in rat liver as a possible explanation of tumor production by nonmutagenic compounds.大鼠肝脏中自发的癌前细胞的促进作用,作为非诱变化合物产生肿瘤的一种可能解释。
Cancer Res. 1983 Feb;43(2):839-44.
10
Effect of chronic ethanol diet on the replication, alkylation, and repair of DNA from hepatocytes and nonparenchymal cells following dimethylnitrosamine administration.慢性乙醇饮食对给予二甲基亚硝胺后肝细胞和非实质细胞DNA复制、烷基化及修复的影响。
Carcinogenesis. 1982;3(11):1293-7. doi: 10.1093/carcin/3.11.1293.