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在扩散室内使用肝微粒体的体外代谢活化测定法:环磷酰胺或异环磷酰胺在培养的人及中国仓鼠细胞中诱发姐妹染色单体交换和染色体畸变。

An in vitro metabolic activation assay using liver microsomes in diffusion chambers: induction of sister chromatid exchanges and chromosome aberrations by cyclophosphamide or ifosfamide in cultured human and Chinese hamster cells.

机构信息

Department of Experimental Biology, Roswell Park Memorial Institute, 666 Elm Street, Buffalo, NY 14263, USA.

出版信息

Carcinogenesis. 1980 Jan;1(1):37-40. doi: 10.1093/carcin/1.1.37.

Abstract

An in vitro activation assay for identifying suspected indirect mutagens and/or carcinogens is described. It involves the incubation of diffusion chambers filled with S-9 mix (S-9 fraction of rat liver and enzyme cofactors) and a compound under test with mammalian cells. The induction of sister chromatid exchanges (SCE) and/or chromosome aberrations can then be used as an indicator of mutagenicity or carcinogenicity. When a human lymphoid cell line, B35M, or Chinese hamster cell lines, V79 and CHO, are cultured with the diffusion chamber containing S-9 mix and the well-known indirect mutagen cyclophosphamide or its analog ifosfamide, a dose related increase in SCE or chromosome aberrations is observed in all the lines. The major advantages of this system over other in vitro activation assays are alleviation of cytotoxicity of S-9 mix and flexibility of treatment time.

摘要

本文描述了一种用于鉴定可疑间接诱变剂和/或致癌物的体外激活检测方法。该方法涉及将充满 S-9 混合液(大鼠肝 S-9 部分和酶辅助因子)和待测试化合物的扩散室与哺乳动物细胞一起孵育。然后可以将姐妹染色单体交换(SCE)和/或染色体畸变用作诱变或致癌性的指标。用人淋巴细胞系 B35M 或中国仓鼠细胞系 V79 和 CHO 与含有 S-9 混合液的扩散室以及众所周知的间接诱变剂环磷酰胺或其类似物异环磷酰胺一起培养时,所有这些细胞系中 SCE 或染色体畸变均呈现出剂量相关性增加。与其他体外激活检测方法相比,该系统的主要优势在于减轻了 S-9 混合液的细胞毒性和处理时间的灵活性。

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