敌敌畏(DDVP)研究。3敌敌畏对小鼠共致癌活性的检测[j]。

Archiv fur Geschwulstforschung Pub Date : 1990-01-01
K H Horn, B Teichmann, T Schramm
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引用次数: 0

摘要

为了明确敌敌畏(DDVP)是否具有共致癌性,我们对C57Bl/6/Bln菌株的雄性和雌性小鼠皮下注射致癌物n -亚硝基二乙胺(NDEA),并口服敌敌畏。其他各组小鼠单独给予NDEA和DDVP进行比较。与NDEA处理组相比,联合应用(NDEA + DDVP)没有导致肿瘤和肿瘤前病变的发生率增加。与单一复合治疗组相比,NDEA + DDVP组膀胱上皮局灶性(移行细胞)增生的发生率增加。NDEA + DDVP联合治疗无肿瘤发生,肿瘤潜伏期无差异。在此实验条件下,DDVP对小鼠无共致癌作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Studies on dichlorvos (DDVP). III. Testing of dichlorvos for cocarcinogenic activity in mice].

In order to clarify whether or not Dichlorvos (DDVP)--which did not exert carcinogenic effects in mice in our experiments--is cocarcinogenic, male and female mice of the strain C57Bl/6/Bln were subcutaneously injected with the carcinogen N-Nitrosodiethylamine (NDEA) and received in addition DDVP orally. For comparison NDEA and DDVP alone was administered to other groups of mice. The combined application (NDEA + DDVP) did not result in increased incidences of tumors and preneoplastic lesions as compared with the NDEA-treated groups of mice. The incidence of focal (transitional cell) hyperplasias of the urinary bladder epithelium was increased in the groups treated with NDEA + DDVP as compared to the groups with single compound treatment. There were no development of tumors and no differences in the latency periods of tumors which could be attributed to the combined treatment with NDEA + DDVP. Under these experimental conditions DDVP was not cocarcinogenic in mice.

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