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2
Trihalomethanes as initiators and promoters of carcinogenesis.三卤甲烷作为致癌作用的引发剂和促进剂。
Environ Health Perspect. 1982 Dec;46:151-6. doi: 10.1289/ehp.8246151.
3
Ethylene dichloride: a review of its metabolism, mutagenic and carcinogenic potential.二氯乙烷:对其代谢、致突变性和致癌潜力的综述。
Drug Chem Toxicol. 1982;5(4):319-88. doi: 10.3109/01480548208993190.
4
In vivo genotoxicity and acute hepatotoxicity of 1,2-dichloroethane in mice: comparison of oral, intraperitoneal, and inhalation routes of exposure.
Cancer Res. 1984 Oct;44(10):4267-71.
5
Application of quantitative stereology to the evaluation of enzyme-altered foci in rat liver.定量体视学在大鼠肝脏酶改变灶评估中的应用。
Cancer Res. 1982 Feb;42(2):465-72.
6
Carcinogenicity studies on halogenated hydrocarbons.卤代烃的致癌性研究。
Environ Health Perspect. 1977 Dec;21:7-16. doi: 10.1289/ehp.77217.

饮用水中给予小鼠的氯代甲烷和乙烷化合物的致癌性。

Carcinogenicity of chlorinated methane and ethane compounds administered in drinking water to mice.

作者信息

Klaunig J E, Ruch R J, Pereira M A

出版信息

Environ Health Perspect. 1986 Nov;69:89-95. doi: 10.1289/ehp.866989.

DOI:10.1289/ehp.866989
PMID:3816740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1474300/
Abstract

The chlorinated hydrocarbons chloroform (CHCl3), 1,1-dichlorethane (1,1-DCE) and 1,2-dichloroethane (1,2-DCE) have been detected in finished drinking water. When administered to B6C3F1 mice by gavage in corn oil, these compounds have been shown to induce hepatic tumors. The present study examines the effect on liver tumor incidence of continuous treatment of CHCl3 (600 mg/L and 1800 mg/L), 1,1-DCE (835 mg/L and 2500 mg/L), and 1,2-DCE (835 mg/L and 2500 mg/L) administered in drinking water to male B6C3F1 mice using a two-stage (initiation/promotion) treatment protocol. Seventy 4-week-old male B6C3F1 mice constituted each treatment group. Of these mice, 35 were initiated by treatment with diethylnitrosamine (DENA) (10 mg/L) in the drinking water for 4 weeks. The remaining 35 received deionized drinking water. Each group was subsequently treated with one of two concentrations of CHCl3, 1,1-DCE, or 1,2-DCE in drinking water for 52 weeks. An additional group received phenobarbital (PB) (500 mg/L) and served as the positive control for liver tumor promotion. Mice were sampled after 24 weeks (10 mice) and 52 weeks (25 mice). At sampling, liver and lung tumors were detected. None of the compounds increased the number or incidence of lung or liver tumors by themselves. PB promoted liver tumor formation (but not lung tumors) in the DENA-initiated mice. 1,1-DCE and 1,2-DCE did not affect the incidence or number of liver or lung tumors in the DENA-initiated animals. CHCl3, however, inhibited liver and lung tumorigenesis in the DENA-initiated mice.

摘要

在成品饮用水中已检测到氯代烃氯仿(CHCl₃)、1,1 - 二氯乙烷(1,1 - DCE)和1,2 - 二氯乙烷(1,2 - DCE)。当通过玉米油灌胃给予B6C3F1小鼠时,这些化合物已被证明可诱发肝肿瘤。本研究使用两阶段(启动/促癌)治疗方案,研究了饮用水中连续给予CHCl₃(600 mg/L和1800 mg/L)、1,1 - DCE(835 mg/L和2500 mg/L)以及1,2 - DCE(835 mg/L和2500 mg/L)对雄性B6C3F1小鼠肝脏肿瘤发生率的影响。每个治疗组由70只4周龄的雄性B6C3F1小鼠组成。在这些小鼠中,35只通过饮用含二乙基亚硝胺(DENA)(10 mg/L)的水进行4周处理来启动。其余35只饮用去离子水。随后,每组用饮用水中两种浓度之一的CHCl₃、1,1 - DCE或1,2 - DCE处理52周。另一组接受苯巴比妥(PB)(500 mg/L)并作为肝脏肿瘤促癌的阳性对照。在24周(10只小鼠)和52周(25只小鼠)后对小鼠进行采样。在采样时,检测肝脏和肺部肿瘤。这些化合物单独使用时均未增加肺部或肝脏肿瘤的数量或发生率。PB促进了DENA启动的小鼠肝脏肿瘤的形成(但不促进肺部肿瘤)。1,1 - DCE和1,2 - DCE对DENA启动的动物肝脏或肺部肿瘤的发生率或数量没有影响。然而,CHCl₃抑制了DENA启动的小鼠肝脏和肺部肿瘤的发生。