• 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

在饮用水中给予F344大鼠辣根提取物会促进膀胱癌发生。

Horseradish extract promotes urinary bladder carcinogenesis when administered to F344 rats in drinking water.

作者信息

Cho Young-Man, Hasumura Mai, Imai Toshio, Takami Shigeaki, Nishikawa Akiyoshi, Ogawa Kumiko

机构信息

Division of Pathology, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-Ku, Tokyo, 158-8501, Japan.

Central Animal Division, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

出版信息

J Appl Toxicol. 2017 Jul;37(7):853-862. doi: 10.1002/jat.3434. Epub 2017 Feb 6.

DOI:10.1002/jat.3434
PMID:28165151
Abstract

Horseradish extract (HRE), consisting mainly of a mixture of allyl isothiocyanate and other isothiocyanates, has been used as a food additive. To evaluate the potential hazards of HRE, a 104-week chronic study, a 2-week analysis of cell proliferation in the urinary bladder and a medium-term promotion bioassay of HRE were conducted with administration at concentrations of up to 0.04% HRE in the drinking water to male F344 rats. In the 104-week chronic study with 32 male rats per group, no treatment-related increases in the incidences of neoplastic lesions in any organ, including urinary bladder, were observed, except for simple hyperplasia in the urinary bladder in rats treated with HRE at concentrations of more than 0.01% (5.0 mg kg body weight day ). In the promotion study, HRE treatment after N-butyl-N-(4-hydroxybutyl)nitrosamine initiation caused a clear increase in papillary or nodular hyperplasia, papilloma, and urothelial carcinoma of the urinary bladder in the groups given HRE for 13 weeks at doses higher than 0.005%, 0.01%, and 0.04% (2.7, 5.4 and 20.5 mg kg body weight day ), respectively. In the 2-week cell proliferation analysis, treatment with HRE at concentrations greater than 0.005% (3.9 mg kg body weight day ) caused transient increases in 5-bromo-2'-deoxyuridine labeling indices in the urothelium. Although clear tumor induction was not observed, administration of relatively low-dose HRE increased cell proliferation in the urothelium and exerted obvious promoting effects on rat urinary bladder carcinogenesis. Further studies are needed to elucidate the mode of action of HRE in the rat urinary bladder to facilitate data extrapolation from the present study and provide insights into risk assessment. Copyright © 2017 John Wiley & Sons, Ltd.

摘要

辣根提取物(HRE)主要由异硫氰酸烯丙酯和其他异硫氰酸酯的混合物组成,已被用作食品添加剂。为评估HRE的潜在危害,对雄性F344大鼠进行了一项为期104周的慢性研究、一项为期2周的膀胱细胞增殖分析以及一项HRE中期促癌生物测定,饮用水中HRE的给药浓度高达0.04%。在每组32只雄性大鼠的104周慢性研究中,未观察到任何器官(包括膀胱)肿瘤性病变发生率有与治疗相关的增加,但在接受浓度超过0.01%(5.0毫克/千克体重/天)HRE治疗的大鼠膀胱中出现了单纯性增生。在促癌研究中,在给予高于0.005%、0.01%和0.04%(2.7、5.4和20.5毫克/千克体重/天)剂量的HRE 13周的组中,用N-丁基-N-(4-羟丁基)亚硝胺启动后进行HRE治疗导致膀胱乳头状或结节状增生、乳头状瘤和尿路上皮癌明显增加。在为期2周的细胞增殖分析中,浓度大于0.005%(3.9毫克/千克体重/天)的HRE处理导致尿路上皮中5-溴-2'-脱氧尿苷标记指数短暂增加。虽然未观察到明显的肿瘤诱导,但给予相对低剂量的HRE会增加尿路上皮中的细胞增殖,并对大鼠膀胱癌发生产生明显的促进作用。需要进一步研究以阐明HRE在大鼠膀胱中的作用模式,以便从本研究中进行数据外推,并为风险评估提供见解。版权所有©2017约翰威立国际出版公司。

相似文献

1
Horseradish extract promotes urinary bladder carcinogenesis when administered to F344 rats in drinking water.在饮用水中给予F344大鼠辣根提取物会促进膀胱癌发生。
J Appl Toxicol. 2017 Jul;37(7):853-862. doi: 10.1002/jat.3434. Epub 2017 Feb 6.
2
Toxic effects of a horseradish extract and allyl isothiocyanate in the urinary bladder after 13-week administration in drinking water to F344 rats.连续 13 周经饮水给予 F344 大鼠辣根提取物和丙烯基异硫氰酸酯后的膀胱毒性作用。
J Toxicol Sci. 2011;36(6):763-74. doi: 10.2131/jts.36.763.
3
Involvement of toxicity as an early event in urinary bladder carcinogenesis induced by phenethyl isothiocyanate, benzyl isothiocyanate, and analogues in F344 rats.在F344大鼠中,毒性作为苯乙基异硫氰酸酯、苄基异硫氰酸酯及其类似物诱导膀胱癌发生早期事件的参与情况。
Toxicol Pathol. 2003 Jul-Aug;31(4):388-96. doi: 10.1080/01926230390202326.
4
Toxicology and carcinogenesis studies of acrylamide (CASRN 79-06-1) in F344/N rats and B6C3F1 mice (feed and drinking water studies).丙烯酰胺(化学物质登记号79 - 06 - 1)在F344/N大鼠和B6C3F1小鼠中的毒理学与致癌性研究(饲料和饮用水研究)
Natl Toxicol Program Tech Rep Ser. 2012 Jul(575):1-234.
5
NTP Toxicology and Carcinogenesis Studies of 1-Amino-2,4-Dibromoanthraquinone (CAS No. 81-49-2) in F344/N Rats and B6C3F1 Mice (Feed Studies).1-氨基-2,4-二溴蒽醌(CAS编号:81-49-2)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学与致癌性研究(饲料喂养研究)
Natl Toxicol Program Tech Rep Ser. 1996 Aug;383:1-370.
6
Orally administered nicotine effects on rat urinary bladder proliferation and carcinogenesis.经口给予尼古丁对大鼠膀胱增殖和癌变的影响。
Toxicology. 2018 Apr 1;398-399:31-40. doi: 10.1016/j.tox.2018.02.008. Epub 2018 Mar 6.
7
Strong promoting activity of phenylethyl isothiocyanate and benzyl isothiocyanate on urinary bladder carcinogenesis in F344 male rats.苯乙基异硫氰酸酯和苄基异硫氰酸酯对F344雄性大鼠膀胱癌发生具有强烈的促进作用。
Int J Cancer. 1998 Aug 31;77(5):773-7. doi: 10.1002/(sici)1097-0215(19980831)77:5<773::aid-ijc17>3.0.co;2-2.
8
Toxicology and carcinogenesis studies of Ginkgo biloba extract (CAS No. 90045-36-6) in F344/N rats and B6C3F1/N mice (Gavage studies).银杏叶提取物(CAS编号90045-36-6)在F344/N大鼠和B6C3F1/N小鼠中的毒理学和致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 2013 Mar(578):1-183.
9
Ethanol-extracted propolis enhances BBN-initiated urinary bladder carcinogenesis via non-mutagenic mechanisms in rats.乙醇提取的蜂胶通过非诱变机制增强大鼠中由N-丁基-N-(4-羟基丁基)亚硝胺引发的膀胱癌发生。
Food Chem Toxicol. 2015 Sep;83:193-200. doi: 10.1016/j.fct.2015.06.007. Epub 2015 Jun 23.
10
NTP Toxicology and Carcinogenesis Studies of Salicylazosulfapyridine (CAS No. 599-79-1) in F344/N Rats and B6C3F1 Mice (Gavage Studies).柳氮磺胺吡啶(CAS编号:599-79-1)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学与致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 1997 May;457:1-327.

引用本文的文献

1
miR-202 Inhibits Cell Proliferation, Migration, and Invasion by Targeting Epidermal Growth Factor Receptor in Human Bladder Cancer.miR-202 通过靶向表皮生长因子受体抑制人膀胱癌细胞的增殖、迁移和侵袭。
Oncol Res. 2018 Jul 5;26(6):949-957. doi: 10.3727/096504018X15149787144385. Epub 2018 Jan 3.