• 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

Formation of dichloroacetic acid by rat and mouse gut microflora, an in vitro study.

作者信息

Moghaddam A P, Abbas R, Fisher J W, Stavrou S, Lipscomb J C

机构信息

Toxicology Division, Armstrong Laboratory, Wright-Patterson Air Force Base, Ohio 45433-7400, USA.

出版信息

Biochem Biophys Res Commun. 1996 Nov 12;228(2):639-45. doi: 10.1006/bbrc.1996.1709.

DOI:10.1006/bbrc.1996.1709
PMID:8920962
Abstract

Metabolism of trichloroethylene (TRI) and its major metabolite, trichloroacetic acid (TCA), by gut content and gut microflora cultures was studied to gain an insight into the role of enterohepatic circulation in TRI metabolism. TRI and TCA were incubated anaerobically with rat and mouse cecal contents and TCA was additionally incubated anaerobically and aerobically with microflora cultures from mice. Although TRI was not metabolized by rat or mouse cecal contents. TCA was metabolized to dichloroacetic acid (DCA) by cecal contents. DCA formation in microflora cultures was dependent on initial TCA concentration, duration of incubation, and initial bacterial number. DCA was not observed in aerobic cultures exposed to TCA. These results suggest that strict anaerobic microorganisms of the gut may partly be responsible for dechlorination of TCA to DCA.

摘要

相似文献

1
Formation of dichloroacetic acid by rat and mouse gut microflora, an in vitro study.
Biochem Biophys Res Commun. 1996 Nov 12;228(2):639-45. doi: 10.1006/bbrc.1996.1709.
2
Relative formation of dichloroacetate and trichloroacetate from trichloroethylene in male B6C3F1 mice.雄性B6C3F1小鼠中三氯乙烯生成二氯乙酸和三氯乙酸的相对情况。
Toxicol Appl Pharmacol. 1993 Nov;123(1):1-8. doi: 10.1006/taap.1993.1214.
3
Factors affecting species differences in the kinetics of metabolites of trichloroethylene.影响三氯乙烯代谢物动力学物种差异的因素。
J Toxicol Environ Health. 1995 Apr;44(4):435-47. doi: 10.1080/15287399509531972.
4
Kinetics of trichloroacetic acid and dichloroacetic acid in the isolated perfused rat liver.三氯乙酸和二氯乙酸在离体灌注大鼠肝脏中的动力学
Toxicol Appl Pharmacol. 1998 Sep;152(1):90-8. doi: 10.1006/taap.1998.8505.
5
Pharmacokinetic analysis of chloral hydrate and its metabolism in B6C3F1 mice.水合氯醛在B6C3F1小鼠体内的药代动力学分析及其代谢
Drug Metab Dispos. 1996 Dec;24(12):1340-6.
6
The extent of dichloroacetate formation from trichloroethylene, chloral hydrate, trichloroacetate, and trichloroethanol in B6C3F1 mice.B6C3F1小鼠中三氯乙烯、水合氯醛、三氯乙酸和三氯乙醇生成二氯乙酸的程度。
Toxicol Sci. 1998 Sep;45(1):33-41. doi: 10.1006/toxs.1998.2500.
7
NTP technical report on the toxicity and metabolism studies of chloral hydrate (CAS No. 302-17-0). Administered by gavage to F344/N rats and B6C3F1 mice.国家毒理学计划关于水合氯醛(化学物质登记号:302-17-0)毒性和代谢研究的技术报告。通过灌胃法给予F344/N大鼠和B6C3F1小鼠。
Toxic Rep Ser. 1999 Aug(59):1-66, A1-E7.
8
Hypomethylation of DNA and the insulin-like growth factor-II gene in dichloroacetic and trichloroacetic acid-promoted mouse liver tumors.二氯乙酸和三氯乙酸诱发的小鼠肝肿瘤中DNA及胰岛素样生长因子-II基因的低甲基化
Toxicology. 2004 Mar 1;196(1-2):127-36. doi: 10.1016/j.tox.2003.11.011.
9
A physiologically based pharmacokinetic model for trichloroethylene and its metabolites, chloral hydrate, trichloroacetate, dichloroacetate, trichloroethanol, and trichloroethanol glucuronide in B6C3F1 mice.B6C3F1小鼠中三氯乙烯及其代谢产物水合氯醛、三氯乙酸、二氯乙酸、三氯乙醇和三氯乙醇葡萄糖醛酸苷的基于生理学的药代动力学模型。
Toxicol Appl Pharmacol. 1997 Nov;147(1):15-30. doi: 10.1006/taap.1997.8190.
10
Kinetics of chloral hydrate and its metabolites in male human volunteers.水合氯醛及其代谢产物在男性人类志愿者体内的动力学
Toxicology. 2008 Mar 12;245(1-2):130-40. doi: 10.1016/j.tox.2007.12.018. Epub 2007 Dec 28.

引用本文的文献

1
Anaerobic Microbial Metabolism of Dichloroacetate.二氯乙酸的厌氧微生物代谢。
mBio. 2021 Apr 27;12(2):e00537-21. doi: 10.1128/mBio.00537-21.
2
Trichloroethylene biotransformation and its role in mutagenicity, carcinogenicity and target organ toxicity.三氯乙烯的生物转化及其在致突变性、致癌性和靶器官毒性中的作用。
Mutat Res Rev Mutat Res. 2014 Oct-Dec;762:22-36. doi: 10.1016/j.mrrev.2014.04.003.
3
Pharmacokinetic analysis of trichloroethylene metabolism in male B6C3F1 mice: Formation and disposition of trichloroacetic acid, dichloroacetic acid, S-(1,2-dichlorovinyl)glutathione and S-(1,2-dichlorovinyl)-L-cysteine.
雄性B6C3F1小鼠中三氯乙烯代谢的药代动力学分析:三氯乙酸、二氯乙酸、S-(1,2-二氯乙烯基)谷胱甘肽和S-(1,2-二氯乙烯基)-L-半胱氨酸的形成与处置
Toxicol Appl Pharmacol. 2009 Jul 1;238(1):90-9. doi: 10.1016/j.taap.2009.04.019. Epub 2009 May 3.
4
Issues in the pharmacokinetics of trichloroethylene and its metabolites.三氯乙烯及其代谢物的药代动力学问题
Environ Health Perspect. 2006 Sep;114(9):1450-6. doi: 10.1289/ehp.8691.
5
Metabolism of trichloroethylene.三氯乙烯的代谢
Environ Health Perspect. 2000 May;108 Suppl 2(Suppl 2):177-200. doi: 10.1289/ehp.00108s2177.