• 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

Involvement of the intestinal microflora in nitrazepam-induced teratogenicity in rats and its relationship to nitroreduction.

作者信息

Takeno S, Sakai T

机构信息

Department of Pharmacology, School of Pharmacy, Hokuriku University, Kanazawa, Japan.

出版信息

Teratology. 1991 Aug;44(2):209-14. doi: 10.1002/tera.1420440209.

DOI:10.1002/tera.1420440209
PMID:1925980
Abstract

A study was undertaken to investigate the relationship between nitroreduction of nitrazepam and its teratogenic effects and the involvement of the intestinal microflora in Sprague-Dawley rats. Incubation of bacterial suspensions from rat cecal contents with nitrazepam resulted in extensive reduction to 7-aminonitrazepam. Rat liver homogenates also reduced nitrazepam but only under anaerobic conditions. Following oral administration of 300 mg/kg nitrazepam to pregnant rats, total excretion of reduced metabolites (7-aminonitrazepam and 7-acetylaminonitrazepam) in urine and feces accounted for approximately 30% of the administered dose. When antibiotics were administered to dams to deplete their intestinal microflora prior to administration to nitrazepam, the total excretion of the reduced metabolites in the urine and feces decreased to 2% of the dose. Nitroreductase activity of cecal contents was almost completely suppressed by antibiotic pretreatment, but the activity of liver homogenates was not significantly altered by the same treatment. The incidence of nitrazepam-induced malformations was markedly decreased by antibiotic pretreatment. These results suggest that the intestinal microflora plays an important role in the reductive metabolism of nitrazepam and that the teratogenicity of nitrazepam may be related to its nitroreduction by the microflora.

摘要

相似文献

1
Involvement of the intestinal microflora in nitrazepam-induced teratogenicity in rats and its relationship to nitroreduction.
Teratology. 1991 Aug;44(2):209-14. doi: 10.1002/tera.1420440209.
2
Teratogenic effects of nitrazepam in rats.硝西泮对大鼠的致畸作用。
Res Commun Chem Pathol Pharmacol. 1990 Jul;69(1):59-70.
3
Role of the intestinal microflora in clonazepam metabolism in the rat.肠道微生物群在大鼠氯硝西泮代谢中的作用。
Xenobiotica. 1984 Nov;14(11):829-40. doi: 10.3109/00498258409151481.
4
Characterization of Escherichia coli nitroreductase NfsB in the metabolism of nitrobenzodiazepines.大肠杆菌硝基还原酶NfsB在硝基苯二氮䓬代谢中的特性研究
Biochem Pharmacol. 2009 Jul 1;78(1):96-103. doi: 10.1016/j.bcp.2009.03.019. Epub 2009 Mar 31.
5
Comparative developmental toxicity and metabolism of nitrazepam in rats and mice.硝西泮在大鼠和小鼠中的发育毒性及代谢比较
Toxicol Appl Pharmacol. 1993 Aug;121(2):233-8. doi: 10.1006/taap.1993.1150.
6
Nitroreduction and formation of hemoglobin adducts in rats with a human intestinal microflora.具有人类肠道微生物群的大鼠体内血红蛋白加合物的硝基还原及形成
Environ Health Perspect. 1994 Oct;102 Suppl 6(Suppl 6):39-41. doi: 10.1289/ehp.94102s639.
7
Metabolism and excretion of trovafloxacin, a new quinolone antibiotic, in Sprague-Dawley rats and beagle dogs. Effect of bile duct cannulation on excretion pathways.新型喹诺酮类抗生素曲伐沙星在斯普拉格-道利大鼠和比格犬体内的代谢与排泄。胆管插管对排泄途径的影响。
Drug Metab Dispos. 1996 Nov;24(11):1231-40.
8
NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.美国国家毒理学计划关于邻苯二甲酸二丁酯(化学物质登记号84 - 74 - 2)经饲料给予F344/N大鼠和B6C3F1小鼠的毒性研究技术报告。
Toxic Rep Ser. 1995 Apr;30:1-G5.
9
Feeding potato flakes affects cecal short-chain fatty acids, microflora and fecal bile acids in rats.喂食马铃薯片会影响大鼠盲肠中的短链脂肪酸、微生物群和粪便中的胆汁酸。
Ann Nutr Metab. 2008;52(1):1-7. doi: 10.1159/000114288. Epub 2008 Jan 30.
10
NTP Technical Report on the metabolism, toxicity and predicted carcinogenicity of diazoaminobenzene (CAS No. 136-35-6).美国国家毒理学计划关于重氮氨基苯(化学物质登记号:136-35-6)的代谢、毒性及预测致癌性的技术报告
Toxic Rep Ser. 2002 Sep(73):1-23, A1-C6.

引用本文的文献

1
Microbial metabolism marvels: a comprehensive review of microbial drug transformation capabilities.微生物代谢的奇迹:微生物药物转化能力的综合评述。
Gut Microbes. 2024 Jan-Dec;16(1):2387400. doi: 10.1080/19490976.2024.2387400. Epub 2024 Aug 16.
2
Past, present, and future of microbiome-based therapies.基于微生物群的疗法的过去、现在和未来。
Microbiome Res Rep. 2024 Mar 18;3(2):23. doi: 10.20517/mrr.2023.80. eCollection 2024.
3
Dissecting the human gut microbiome to better decipher drug liability: A once-forgotten organ takes center stage.
剖析人类肠道微生物群以更好地解读药物安全性:一个曾被遗忘的器官成为焦点。
J Adv Res. 2023 Oct;52:171-201. doi: 10.1016/j.jare.2023.07.002. Epub 2023 Jul 5.
4
The Interplay between Gut Microbiota and Oral Medications and Its Impact on Advancing Precision Medicine.肠道微生物群与口服药物之间的相互作用及其对推进精准医学的影响。
Metabolites. 2023 May 21;13(5):674. doi: 10.3390/metabo13050674.
5
Biotransformation novel advances - 2021 year in review.生物转化新进展——2021 年回顾。
Drug Metab Rev. 2022 Aug;54(3):207-245. doi: 10.1080/03602532.2022.2097253. Epub 2022 Aug 30.
6
Effect of 6-Methoxybenzoxazolinone on the Cecal Microbiota of Adult Male Brandt's Vole.6-甲氧基苯并恶唑啉酮对成年雄性布氏田鼠盲肠微生物群的影响。
Front Microbiol. 2022 Mar 29;13:847073. doi: 10.3389/fmicb.2022.847073. eCollection 2022.
7
Microbiota-Gut-Brain Axis and Epilepsy: A Review on Mechanisms and Potential Therapeutics.微生物群-肠道-脑轴与癫痫:机制与潜在治疗策略的综述。
Front Immunol. 2021 Oct 11;12:742449. doi: 10.3389/fimmu.2021.742449. eCollection 2021.
8
Gastrointestinal biofilms in health and disease.肠道生物膜:健康与疾病。
Nat Rev Gastroenterol Hepatol. 2021 May;18(5):314-334. doi: 10.1038/s41575-020-00397-y. Epub 2021 Jan 28.
9
Bioavailability Based on the Gut Microbiota: a New Perspective.基于肠道菌群的生物利用度:一个新视角。
Microbiol Mol Biol Rev. 2020 Apr 29;84(2). doi: 10.1128/MMBR.00072-19. Print 2020 May 20.
10
The gut microbiome: an orchestrator of xenobiotic metabolism.肠道微生物群:外源性物质代谢的协调者。
Acta Pharm Sin B. 2020 Jan;10(1):19-32. doi: 10.1016/j.apsb.2019.12.001. Epub 2019 Dec 10.