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硫酸肼作为致癌物在lacZ转基因小鼠靶组织中的体内非致突变性证据。

Evidence for in vivo non-mutagenicity of the carcinogen hydrazine sulfate in target tissues of lacZ transgenic mice.

作者信息

Douglas G R, Gingerich J D, Soper L M

机构信息

Mutagenesis Section, Health Canada, Ottawa, Ontario.

出版信息

Carcinogenesis. 1995 Apr;16(4):801-4. doi: 10.1093/carcin/16.4.801.

Abstract

Transgenic mouse models permit the confirmation of in vitro mutagenicity in vivo without the constraints in the selection of tissues imposed by other in vivo assays. This feature is of particular importance in the determination of mutagenicity in the target tissues of carcinogens, especially those that are in vitro mutagens. Such information is critical in the determination of whether a chemical is carcinogenic via a genotoxic or non-genotoxic mechanism. Hydrazine sulfate is an in vitro mutagen that induces lung and liver tumours in mice. Transgenic mice from strain 40.6 (Mutamouse) were administered single oral doses up to a toxic concentration (400 mg/kg). No dose induced any lacZ mutations in lung, liver or bone marrow. Since the highest single dose used is higher than the cumulative dose that induced tumours in previous studies, it may be that either hydrazine sulfate is genotoxic in target tissues in vivo only when given in multiple doses or that it is a non-genotoxic carcinogen.

摘要

转基因小鼠模型能够在体内证实体外诱变性,而不存在其他体内试验在组织选择上的限制。这一特性在确定致癌物靶组织中的诱变性时尤为重要,尤其是那些体外诱变剂。此类信息对于确定一种化学物质是通过遗传毒性还是非遗传毒性机制致癌至关重要。硫酸肼是一种体外诱变剂,可在小鼠体内诱发肺和肝肿瘤。给40.6品系(突变小鼠)的转基因小鼠单次口服高达毒性浓度(400毫克/千克)的剂量。没有任何剂量在肺、肝或骨髓中诱导出任何lacZ突变。由于所使用的最高单次剂量高于先前研究中诱导肿瘤的累积剂量,可能是硫酸肼仅在多次给药时才在体内靶组织中具有遗传毒性,或者它是一种非遗传毒性致癌物。

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