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Genotoxicity, toxicity, and carcinogenicity of the antihistamine methapyrilene.

作者信息

Mirsalis J C

出版信息

Mutat Res. 1987 May;185(3):309-17. doi: 10.1016/0165-1110(87)90022-4.

DOI:10.1016/0165-1110(87)90022-4
PMID:3553919
Abstract

The antihistamine methapyrilene hydrochloride (MP) has been shown to be a potent hepatocarcinogen in rats, but not in hamsters or guinea pigs. This finding is in contrast to the relative nongenotoxicity of this compound. MP has been evaluated for genotoxicity in a wide variety of short-term tests and has generally demonstrated little genotoxic activity. One exception to this is the mouse lymphoma L5178Y mutagenesis assay, in which MP produced a very significant increase in small colony mutants with concomitant chromosomal damage in these cells. MP also induced positive responses in several cell transformation assays. One potentially very significant effect of MP is that it induces a large increase in hepatic cell proliferation coupled with mitochondrial proliferation in the livers of treated animals. This effect is discussed as a possible mechanism of liver tumor induction in rats.

摘要

相似文献

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Mutat Res. 1987 May;185(3):309-17. doi: 10.1016/0165-1110(87)90022-4.
2
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Toxic Rep Ser. 2000 Feb;46:1-C7.
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