• 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

Organ variation in the mutagenicity of MeIQ in Big Blue lacI transgenic mice.

作者信息

Suzuki T, Hayashi M, Ochiai M, Wakabayashi K, Ushijima T, Sugimura T, Nagao M, Sofuni T

机构信息

Division of Genetics and Mutagenesis, National Institute of Health Sciences, Tokyo, Japan.

出版信息

Mutat Res. 1996 Jul 10;369(1-2):45-9. doi: 10.1016/s0165-1218(96)90046-4.

DOI:10.1016/s0165-1218(96)90046-4
PMID:8700181
Abstract

2-Amino-3,4-dimethylimidazo[4,5-f]quinoline (MeIQ), which is a heterocyclic amine found in food and the potent mutagen in S. typhimurium TA98, was examined for its genotoxic potential using lacI transgenic mice (Big Blue, C57BL/6N lineage). Female mice, at 7 weeks of age, were given a diet containing 0.03% MeIQ for 1, 4 and 12 weeks, and mutant frequencies (MF) were analyzed in the bone marrow, liver, forestomach, colon and heart. The MF increased in a feeding period-dependent manner. Relative to untreated mice, the MF after a 12-week-feeding of MeIQ was 38 times higher in the colon, 5.8 times higher in the bone marrow, 4.6 times higher in the liver, and 2.6 times higher in the forestomach. No increase in MF was detected in the heart, where no tumors develop.

摘要

相似文献

1
Organ variation in the mutagenicity of MeIQ in Big Blue lacI transgenic mice.
Mutat Res. 1996 Jul 10;369(1-2):45-9. doi: 10.1016/s0165-1218(96)90046-4.
2
DNA adduct level induced by 2-amino-3,4-dimethylimidazo[4,5-f]-quinoline in Big Blue mice does not correlate with mutagenicity.
Mutagenesis. 1998 Jul;13(4):381-4. doi: 10.1093/mutage/13.4.381.
3
No direct correlation between mutant frequencies and cancer incidence induced by MeIQ in various organs of Big Blue mice.
Mutat Res. 1998 May 25;400(1-2):251-7. doi: 10.1016/s0027-5107(98)00032-3.
4
In vivo genotoxicity of 2-amino-3,8-dimethylimidazo[4, 5-f]quinoxaline in lacI transgenic (Big Blue) mice.2-氨基-3,8-二甲基咪唑并[4,5-f]喹喔啉在lacI转基因(大蓝)小鼠体内的遗传毒性
Mutat Res. 2000 Jun 22;468(1):19-25. doi: 10.1016/s1383-5718(00)00036-x.
5
Regional mutagenicity of heterocyclic amines in the intestine: mutation analysis of the cII gene in lambda/lacZ transgenic mice.杂环胺在肠道中的区域致突变性:λ/lacZ转基因小鼠中cII基因的突变分析
Mutat Res. 2003 Aug 5;539(1-2):99-108. doi: 10.1016/s1383-5718(03)00134-7.
6
Genotoxic activity of the N-acetylated metabolites of the food mutagens 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) and 2-amino-3,4-dimethylimidazo[4,5-f]quinoline (MeIQ).食品诱变剂2-氨基-3-甲基咪唑[4,5-f]喹啉(IQ)和2-氨基-3,4-二甲基咪唑[4,5-f]喹啉(MeIQ)的N-乙酰化代谢产物的遗传毒性活性。
Mutagenesis. 1988 Jul;3(4):303-9. doi: 10.1093/mutage/3.4.303.
7
Induction of hepatocellular carcinoma and highly metastatic squamous cell carcinomas in the forestomach of mice by feeding 2-amino-3,4-dimethylimidazo[4,5-f]quinoline.通过喂食2-氨基-3,4-二甲基咪唑[4,5-f]喹啉诱导小鼠前胃肝细胞癌和高转移性鳞状细胞癌。
Carcinogenesis. 1986 Nov;7(11):1889-93. doi: 10.1093/carcin/7.11.1889.
8
Tissue-specific mutational spectra of 2-amino-3,4-dimethylimidazo[4,5-f]quinoline in the liver and bone marrow of lacI transgenic mice.
Carcinogenesis. 1994 Dec;15(12):2805-9. doi: 10.1093/carcin/15.12.2805.
9
Mutational analysis of the liver, colon and kidney of Big Blue rats treated with 2-amino-3-methylimidazo[4,5-f]quinoline.
Carcinogenesis. 2000 Jan;21(1):1-6. doi: 10.1093/carcin/21.1.1.
10
Chromosome aberrations induced in mice by chronic feeding of 2-amino-3,4-dimethylimidazo[4,5-f]quinoline (MeIQ).通过长期喂食2-氨基-3,4-二甲基咪唑[4,5-f]喹啉(MeIQ)诱导小鼠产生的染色体畸变。
Food Chem Toxicol. 1998 Jun;36(6):467-74. doi: 10.1016/s0278-6915(98)00003-9.

引用本文的文献

1
Mutagenicity of carcinogenic heterocyclic amines in Salmonella typhimurium YG strains and transgenic rodents including gpt delta.致癌性杂环胺在鼠伤寒沙门氏菌YG菌株及包括gpt delta在内的转基因啮齿动物中的致突变性。
Genes Environ. 2021 Sep 16;43(1):38. doi: 10.1186/s41021-021-00207-0.
2
Estimating the carcinogenic potency of chemicals from the in vivo micronucleus test.通过体内微核试验评估化学物质的致癌潜力。
Mutagenesis. 2016 May;31(3):347-58. doi: 10.1093/mutage/gev043. Epub 2015 Jul 10.