• 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

苯并[a]芘对哺乳动物细胞(CHO/HGPRT系统)细胞毒性和致突变性的定量分析。

Quantitative analysis of cytotoxicity and mutagenicity of benzo[a]pyrene in mammalian cells (CHO/HGPRT system).

作者信息

Machanoff R, O'Neill J P, Hsie A W

出版信息

Chem Biol Interact. 1981 Feb;34(1):1-10. doi: 10.1016/0009-2797(81)90084-3.

DOI:10.1016/0009-2797(81)90084-3
PMID:7460073
Abstract

Chinese hamster ovary (CHO) cells in cell culture were utilized to study the cytotoxic and mutagenic activity of benzo[a]pyrene (BP). A liver homogenate (S9) prepared from Arochlor 1254 induced male Sprague-Dawley rats was employed to mediate the biotransformation of the promutagen. The dependence of the induction of 6-thioguanine(TG)-resistant mutants on parameters such as BP concentration, amount of S9 protein, ionic composition of the S9 mix and treatment time was determined. Under optimal conditions with a 5-h treatment time, BP mutagenicity can be described as 185 mutants/10(6) cells per microM BP per mg/ml S9 protein.

摘要

利用细胞培养中的中国仓鼠卵巢(CHO)细胞来研究苯并[a]芘(BP)的细胞毒性和诱变活性。使用从经Arochlor 1254诱导的雄性Sprague-Dawley大鼠制备的肝匀浆(S9)来介导前诱变剂的生物转化。确定了6-硫鸟嘌呤(TG)抗性突变体的诱导对诸如BP浓度、S9蛋白量、S9混合物的离子组成和处理时间等参数的依赖性。在处理时间为5小时的最佳条件下,BP的诱变性可描述为每微摩尔BP每毫克/毫升S9蛋白产生185个突变体/10(6)个细胞。

相似文献

1
Quantitative analysis of cytotoxicity and mutagenicity of benzo[a]pyrene in mammalian cells (CHO/HGPRT system).苯并[a]芘对哺乳动物细胞(CHO/HGPRT系统)细胞毒性和致突变性的定量分析。
Chem Biol Interact. 1981 Feb;34(1):1-10. doi: 10.1016/0009-2797(81)90084-3.
2
Cytotoxicity and mutagenicity of dimethylnitrosamine in mammalian cells (CHO/HGPRT system); enhancement by calcium phosphate.
Environ Mutagen. 1982;4(1):7-18. doi: 10.1002/em.2860040103.
3
Cytotoxicity and mutagenicity of coal oils in the CHO/HGPRT assay.煤焦油在CHO/HGPRT试验中的细胞毒性和致突变性。
Environ Mutagen. 1984;6(4):517-27. doi: 10.1002/em.2860060405.
4
Inhibition of the mutagenicity of benzo[a]pyrene in the V79/HGPRT system by bioantioxidants.
Mutat Res. 1984 Jul;137(1):57-9. doi: 10.1016/0165-1218(84)90113-7.
5
Modulation of the cytotoxicity and mutagenicity of benzo[a]pyrene and benzo[a]pyrene 7,8-diol by glutathione and glutathione S-transferases in mammalian cells (CHO/HGPRT assay).
Mutat Res. 1987 Jun;178(2):257-69. doi: 10.1016/0027-5107(87)90276-4.
6
Metabolic activation to a mutagen of 3-hydroxy-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene, a secondary metabolite of benzo[a]pyrene.苯并[a]芘的次级代谢产物3-羟基-反式-7,8-二羟基-7,8-二氢苯并[a]芘向诱变剂的代谢活化。
Carcinogenesis. 1987 Nov;8(11):1621-7. doi: 10.1093/carcin/8.11.1621.
7
Mutagenicity of the mononitrobenzo[a]pyrenes in Chinese hamster ovary cells mediated by rat hepatocytes or liver S9.
Carcinogenesis. 1986 Apr;7(4):681-4. doi: 10.1093/carcin/7.4.681.
8
Effect of metabolic activation on the cytotoxicity and mutagenicity of 1,2-dibromoethane in the CHO/HGPRT system.
Mutat Res. 1982 Aug;95(2-3):377-88. doi: 10.1016/0027-5107(82)90272-x.
9
Glucuronide conjugation reduces the cytotoxicity but not the mutagenicity of benzo(a)pyrene in the CHO/HGPRT assay.在CHO/HGPRT试验中,葡萄糖醛酸结合反应降低了苯并(a)芘的细胞毒性,但未降低其致突变性。
Teratog Carcinog Mutagen. 1984;4(5):391-402. doi: 10.1002/tcm.1770040503.
10
Use of Aroclor 1254-induced rat liver homogenate in the assaying of promutagens in Chinese hamster ovary cells.
Environ Mutagen. 1984;6(4):539-44. doi: 10.1002/em.2860060407.

引用本文的文献

1
Nitroxide TEMPO: a genotoxic and oxidative stress inducer in cultured cells.氮氧自由基 TEMPO:一种培养细胞中的遗传毒性和氧化应激诱导剂。
Toxicol In Vitro. 2013 Aug;27(5):1496-502. doi: 10.1016/j.tiv.2013.02.019. Epub 2013 Mar 18.
2
Measurement of low levels of x-ray mutagenesis in relation to human disease.与人类疾病相关的低水平X射线诱变的测量。
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4839-43. doi: 10.1073/pnas.83.13.4839.