• 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

通过饮用水给予1,2,3 - 三氯丙烷和1,1,2 - 三氯丙烷的90天毒性研究结果。

Results of a 90-day toxicity study on 1,2,3- and 1,1,2-trichloropropane administered via the drinking water.

作者信息

Villeneuve D C, Chu I, Secours V E, Coté M G, Plaa G L, Valli V E

出版信息

Sci Total Environ. 1985 Dec;47:421-6. doi: 10.1016/0048-9697(85)90346-8.

DOI:10.1016/0048-9697(85)90346-8
PMID:4089609
Abstract

Trichloropropanes have been identified as environmental contaminants in sediments of the Great Lakes region of North America. Since these chemicals had the potential to find their way into drinking water, a 90-day feeding study was carried out in order to determine their subchronic toxicity. Groups of 10 male and 10 female weanling Sprague-Dawley rats were supplied drinking water ad libitum, containing 1,2,3- or 1,1,2-trichloropropane at concentrations of 1, 10, 100 or 1000 mg/L for 13 weeks. Emulphor (0.5%) was used to solubilize the chemicals. At the end of the study, the animals were killed and examined for gross and microscopic changes. Heart, liver, brain, kidney and spleen were excised and weighed. Blood was collected and subjected to a comprehensive hematological analysis. Serum was collected and profiled for changes in 12 biochemical parameters and a portion of liver was used to determined mixed function oxidase activity. Although three animals died during the study, their deaths could not be related to treatment. Decreased growth rate was observed in both sexes of the group receiving 1000 mg/L 1,2,3-trichloropropane. There was an increase in liver, kidney and brain weights (relative to body weight) in rats of both sexes fed 1000 mg/L 1,2,3-trichloropropane. Fatty livers were observed in some of the treated animals but a clear dose-relationship was not evident. An elevation in serum cholesterol was observed in female rats fed the highest dose of 1,2,3-trichloropropane.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

三氯丙烷已被确认为北美五大湖地区沉积物中的环境污染物。由于这些化学物质有可能进入饮用水中,因此进行了一项为期90天的喂养研究,以确定它们的亚慢性毒性。将10只雄性和10只雌性断乳的斯普拉格-道利大鼠分为几组,随意提供饮用水,其中含有浓度为1、10、100或1000mg/L的1,2,3-三氯丙烷或1,1,2-三氯丙烷,持续13周。使用乳化剂(0.5%)来溶解这些化学物质。在研究结束时,处死动物并检查大体和微观变化。取出心脏、肝脏、大脑、肾脏和脾脏并称重。采集血液并进行全面的血液学分析。收集血清并分析12种生化参数的变化,取一部分肝脏测定混合功能氧化酶活性。尽管在研究过程中有3只动物死亡,但它们的死亡与处理无关。接受1000mg/L 1,2,3-三氯丙烷的组中,雌雄两性的生长速率均下降。喂食1000mg/L 1,2,3-三氯丙烷的雌雄大鼠的肝脏、肾脏和大脑重量(相对于体重)均增加。在一些接受处理的动物中观察到脂肪肝,但没有明显的剂量关系。喂食最高剂量1,2,3-三氯丙烷的雌性大鼠血清胆固醇升高。(摘要截断于250字)

相似文献

1
Results of a 90-day toxicity study on 1,2,3- and 1,1,2-trichloropropane administered via the drinking water.通过饮用水给予1,2,3 - 三氯丙烷和1,1,2 - 三氯丙烷的90天毒性研究结果。
Sci Total Environ. 1985 Dec;47:421-6. doi: 10.1016/0048-9697(85)90346-8.
2
NTP carcinogenesis studies of 2,2-bis(bromomethyl)-1,3-propanediol, nitromethane, and 1,2,3-trichloropropane (cas nos. 3296-90-0, 75-52-5, and 96-18-4) in guppies (Poecilia reticulata) and medaka (Oryzias latipes) (Waterborne Studies).2,2 - 双(溴甲基)-1,3 - 丙二醇、硝基甲烷和1,2,3 - 三氯丙烷(化学物质登记号分别为3296 - 90 - 0、75 - 52 - 5和96 - 18 - 4)在孔雀鱼(孔雀鱼)和青鳉(青鳉)中的NTP致癌性研究(水基研究)
Natl Toxicol Program Tech Rep Ser. 2005 Oct(528):1-190.
3
NTP Toxicology and Carcinogenesis of 1,2,3-Trichloropropane (CAS No. 96-18-4) in F344/N Rats and B6C3F1 Mice (Gavage Studies).1,2,3-三氯丙烷(CAS编号96-18-4)对F344/N大鼠和B6C3F1小鼠的NTP毒理学与致癌性研究(灌胃研究)
Natl Toxicol Program Tech Rep Ser. 1993 Aug;384:1-348.
4
Cardiopathic effect of 1,2,3-trichloropropane after subacute and subchronic exposure in rats.大鼠亚急性和亚慢性暴露后1,2,3-三氯丙烷的心脏病变效应。
J Appl Toxicol. 1991 Jun;11(3):179-87. doi: 10.1002/jat.2550110305.
5
Evaluation of the subchronic and reproductive effects of a series of chlorinated propanes in the rat. I. Toxicity of 1,2,3-trichloropropane.一系列氯化丙烷对大鼠的亚慢性和生殖影响评估。I. 1,2,3-三氯丙烷的毒性
J Toxicol Environ Health. 1988;25(3):299-315. doi: 10.1080/15287398809531211.
6
NTP technical report on toxicity studies of urethane in drinking water and urethane in 5% ethanol administered to F344/N rats and B6C3F1 mice.国家毒理学计划关于给F344/N大鼠和B6C3F1小鼠饮用含氨基甲酸乙酯的水以及饮用含5%乙醇的氨基甲酸乙酯的毒性研究技术报告。
Toxic Rep Ser. 1996 Mar(52):1-91, A1-9, B1-9 passim.
7
The subchronic toxicity of tetrachloroethylene (perchloroethylene) administered in the drinking water of rats.在大鼠饮用水中给予四氯乙烯(全氯乙烯)的亚慢性毒性。
Fundam Appl Toxicol. 1986 Jul;7(1):119-25. doi: 10.1016/0272-0590(86)90204-6.
8
Comparative chronic toxicity and carcinogenicity of acrylonitrile by drinking water and oral intubation to Spartan Sprague-Dawley rats.饮用水和经口插管给予丙烯腈对斯帕坦斯普拉格-道利大鼠的慢性毒性和致癌性比较
Toxicol Lett. 2002 Jun 24;132(3):197-219. doi: 10.1016/s0378-4274(02)00073-5.
9
NTP toxicity studies of sodium dichromate dihydrate (CAS No. 7789-12-0) administered in drinking water to male and female F344/N rats and B6C3F1 mice and male BALB/c and am3-C57BL/6 mice.对雄性和雌性F344/N大鼠、B6C3F1小鼠以及雄性BALB/c和am3-C57BL/6小鼠经饮用水给予二水合重铬酸钠(化学物质登记号:7789-12-0)的NTP毒性研究。
Toxic Rep Ser. 2007 Jan(72):1-G4.
10
Ten- and ninety-day toxicity studies of 1,2-dichlorobenzene administered by oral gavage to Sprague-Dawley rats.
Drug Chem Toxicol. 1991;14(1-2):83-112. doi: 10.3109/01480549109017870.

引用本文的文献

1
Identification of acrolein as a novel diagnostic odor biomarker for 1,2,3-trichloropropane-induced hepatotoxicity in Sprague Dawley rats.鉴定丙烯醛作为一种新型诊断性气味生物标志物,用于检测1,2,3-三氯丙烷诱导的斯普拉格-道利大鼠肝毒性。
Toxicol Res. 2024 Jul 13;40(4):639-651. doi: 10.1007/s43188-024-00253-0. eCollection 2024 Oct.
2
Two cases reports: Severe liver injury caused by 1,2,3-trichloropropane poisoning.两则病例报告:1,2,3-三氯丙烷中毒导致的严重肝损伤。
Front Public Health. 2023 Apr 14;11:1171071. doi: 10.3389/fpubh.2023.1171071. eCollection 2023.
3
Safety and efficacy of a feed additive consisting of glyceryl polyethyleneglycol ricinoleate (PEG castor oil) for all animal species (FEFANA asbl).
一种由聚乙二醇蓖麻油酸甘油酯(PEG蓖麻油)组成的饲料添加剂对所有动物种类的安全性和有效性(FEFANA非营利组织)
EFSA J. 2022 Oct 28;20(10):e07433. doi: 10.2903/j.efsa.2022.7433. eCollection 2022 Oct.