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大鼠肝脏病灶以及用于检测氯乙烷和氯乙烯引发及促癌作用的体外试验。

Rat liver foci and in vitro assays to detect initiating and promoting effects of chlorinated ethanes and ethylenes.

作者信息

Milman H A, Story D L, Riccio E S, Sivak A, Tu A S, Williams G M, Tong C, Tyson C A

机构信息

Office of Pesticides and Toxic Substances, U.S. Environmental Protection Agency, Washington, D.C. 20460.

出版信息

Ann N Y Acad Sci. 1988;534:521-30. doi: 10.1111/j.1749-6632.1988.tb30143.x.

Abstract

Nine chlorinated aliphatics (CAs) were examined in a rat liver foci assay for tumor initiating and promoting activities. In this model, young adult male Osborne Mendel rats were first subjected to a partial hepatectomy, the test chemical was then administered at the maximum tolerated dose in the initiation or promotion phase in conjunction with diethylnitrosamine (DEN; 30 mg/kg b.w.) or phenobarbital (PB; 0.05 percent, w/w, in the diet), and gamma glutamyltranspeptidase (GGT) was used as a putative preneoplastic indicator. When administered in the promotion protocol after initiation with DEN, 1,1-dichloroethane, 1,1,2-trichloroethane (1,1,2-TCE), 1,1,2,2-tetrachloroethane (1,1,2,2-TTCE), tetrachloroethylene (TTCY), and hexachloroethane induced significant increases in GGT+-foci above control levels. 1,1,2,2-TTCE, TTCY, and 1,1,2-TCE also induced significant increases in GGT+-foci when administered in the promotion protocol without DEN initiation. Two variants of GGT+-foci were observed: the classical type associated with PB promotion, and the other, which was more diffuse, less intensely stained, resembling foci undergoing redifferentiation and associated with CAs. A number of CAs were also genotoxic in short-term in vitro tests. Taken together, the studies suggest that CAs may be complete carcinogens in vivo with weak initiating activity and stronger promoting activity.

摘要

在一项大鼠肝灶试验中,对九种氯化脂肪族化合物(CAs)的肿瘤引发和促进活性进行了检测。在该模型中,首先对成年雄性奥斯本·孟德尔大鼠进行部分肝切除术,然后在引发或促进阶段,将受试化学品以最大耐受剂量与二乙基亚硝胺(DEN;30mg/kg体重)或苯巴比妥(PB;饮食中0.05%,w/w)联合给药,并使用γ-谷氨酰转肽酶(GGT)作为假定的肿瘤前体指标。在用DEN引发后,按照促进方案给药时,1,1-二氯乙烷、1,1,2-三氯乙烷(1,1,2-TCE)、1,1,2,2-四氯乙烷(1,1,2,2-TTCE)、四氯乙烯(TTCY)和六氯乙烷诱导GGT+灶显著增加,高于对照水平。在无DEN引发的促进方案中给药时,1,1,2,2-TTCE、TTCY和1,1,2-TCE也诱导GGT+灶显著增加。观察到两种GGT+灶变体:一种是与PB促进相关的经典类型,另一种更弥散,染色较浅,类似于正在进行再分化的灶,与CAs相关。许多CAs在短期体外试验中也具有遗传毒性。综合来看,这些研究表明CAs在体内可能是完全致癌物,具有较弱的引发活性和较强的促进活性。

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