• 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

蒽醌类化合物在V79细胞及三种表达细胞色素P450酶的衍生细胞系中的致断裂性

Clastogenicity of anthraquinones in V79 and in three derived cell lines expressing P450 enzymes.

作者信息

Simi S, Morelli S, Gervasi P G, Rainaldi G

机构信息

Genetica e Biochimica Tossicologica, Istituto di Mutagenesi e Differenziamento CNR, Pisa, Italy.

出版信息

Mutat Res. 1995 Aug;347(3-4):151-6. doi: 10.1016/0165-7992(95)00034-8.

DOI:10.1016/0165-7992(95)00034-8
PMID:7565906
Abstract

The clastogenicity of seven anthraquinones was investigated in a V79 Chinese hamster cell line expressing only the reductive pathway enzymes and in three derived cell lines transfected and expressing three rat cytochrome P450 (1A1, 1A2, 2B1). The results have shown that chromosomal aberrations are modulated in similar manner both in parental and transfected V79 cell lines, suggesting that the clastogenicity of these compounds is not mediated by cytochrome P450 dependent monooxygenases.

摘要

在仅表达还原途径酶的V79中国仓鼠细胞系以及转染并表达三种大鼠细胞色素P450(1A1、1A2、2B1)的三个衍生细胞系中,研究了七种蒽醌的致断裂性。结果表明,亲代和转染的V79细胞系中染色体畸变的调节方式相似,这表明这些化合物的致断裂性不是由细胞色素P450依赖性单加氧酶介导的。

相似文献

1
Clastogenicity of anthraquinones in V79 and in three derived cell lines expressing P450 enzymes.蒽醌类化合物在V79细胞及三种表达细胞色素P450酶的衍生细胞系中的致断裂性
Mutat Res. 1995 Aug;347(3-4):151-6. doi: 10.1016/0165-7992(95)00034-8.
2
Biotransformation of the naturally occurring lignan (-)-arctigenin in mammalian cell lines genetically engineered for expression of single cytochrome P450 isoforms.在经过基因工程改造以表达单一细胞色素P450同工型的哺乳动物细胞系中天然存在的木脂素(-)-牛蒡子苷元的生物转化。
Planta Med. 1994 Oct;60(5):441-4. doi: 10.1055/s-2006-959528.
3
Use of V79-derived cell lines expressing cytochrome P-450 activity in the study of genotoxicity of anthraquinones.在蒽醌类化合物遗传毒性研究中使用表达细胞色素P - 450活性的V79衍生细胞系。
Cytotechnology. 1993;11 Suppl 1:S21-3.
4
Cytogenetic effects of promutagens in genetically engineered V79 Chinese hamster cells expressing cytochromes P450.前诱变剂在表达细胞色素P450的基因工程V79中国仓鼠细胞中的细胞遗传学效应。
Eur J Pharmacol. 1993 Apr 1;228(5-6):299-304. doi: 10.1016/0926-6917(93)90064-w.
5
A comparative study of the use of primary Chinese hamster liver cultures and genetically engineered immortal V79 Chinese hamster cell lines expressing rat liver CYP1A1, 1A2 and 2B1 cDNAs in micronucleus assays.在微核试验中使用原代中国仓鼠肝细胞培养物和表达大鼠肝脏CYP1A1、1A2和2B1 cDNA的基因工程永生V79中国仓鼠细胞系的比较研究。
Toxicology. 1993 Oct 5;82(1-3):131-49. doi: 10.1016/0300-483x(93)02608-j.
6
Role of cytochrome P-450 isoenzymes in the bioactivation of hydroxy anthraquinones.细胞色素P-450同工酶在羟基蒽醌生物活化中的作用。
Anticancer Res. 1994 Nov-Dec;14(6B):2597-603.
7
Benzylic hydroxylation of 1-methylpyrene and 1-ethylpyrene by human and rat cytochromes P450 individually expressed in V79 Chinese hamster cells.
Carcinogenesis. 1999 Sep;20(9):1777-85. doi: 10.1093/carcin/20.9.1777.
8
Cytochrome P450 mediated reactions studied in genetically engineered V79 Chinese hamster cells.
Pharmacogenetics. 1995;5 Spec No:S91-6. doi: 10.1097/00008571-199512001-00008.
9
3-aminobenzanthrone, a human metabolite of the environmental pollutant 3-nitrobenzanthrone, forms DNA adducts after metabolic activation by human and rat liver microsomes: evidence for activation by cytochrome P450 1A1 and P450 1A2.3-氨基苯并蒽酮是环境污染物3-硝基苯并蒽酮的一种人体代谢产物,经人和大鼠肝脏微粒体代谢活化后形成DNA加合物:细胞色素P450 1A1和P450 1A2活化的证据。
Chem Res Toxicol. 2004 Aug;17(8):1092-101. doi: 10.1021/tx049912v.
10
The K-region trans-8,9-diol does not significantly contribute as an intermediate in the metabolic activation of dibenzo[a,l]pyrene to DNA-binding metabolites by human cytochrome P450 1A1 or 1B1.K区域反式-8,9-二醇在人细胞色素P450 1A1或1B1将二苯并[a,l]芘代谢活化为与DNA结合的代谢产物的过程中,作为中间体的贡献不显著。
Cancer Res. 1999 Sep 15;59(18):4603-9.

引用本文的文献

1
Marine Anthraquinones: Pharmacological and Toxicological Issues.海洋蒽醌类化合物:药理学和毒理学问题。
Mar Drugs. 2021 May 13;19(5):272. doi: 10.3390/md19050272.
2
3-Allyl-1-{[3-(4-nitro-phen-yl)-4,5-dihydro-1,3-oxazol-5-yl]meth-yl}-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione.3-烯丙基-1-{[3-(4-硝基苯基)-4,5-二氢-1,3-恶唑-5-基]甲基}-1H-蒽并[1,2-d]咪唑-2,6,11(3H)-三酮
Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 1;67(Pt 6):o1363-4. doi: 10.1107/S1600536811016606. Epub 2011 May 7.