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α-六氯环己烷或部分肝切除对大鼠肝脏细胞增殖的刺激作用以及在G1期β-二乙氨基乙基苯基二烯丙基乙酸酯盐酸盐(CFT 1201)、β-二乙氨基乙基二苯基丙基乙酸酯盐酸盐(SKF 525-A)和放线菌素D抑制作用的终点。

Stimulation of cell proliferation in rat liver by alpha-hexachlorocyclohexane or partial hepatectomy and end points during G1 of the inhibitory action of beta-diethyl-aminoethylphenyldiallyl acetate-HC1 (CFT 1201), beta-diethylaminoethyldiphenylpropyl acetate. HC1 (SKF 525-A) and actinomycin D.

作者信息

Schulte-Hermann R, Leberl C, Ruberg I

出版信息

Biochim Biophys Acta. 1976 Nov 1;447(4):413-24. doi: 10.1016/0005-2787(76)90079-4.

Abstract

The present work was designed to study the nature, sequence and temporal position of some inhibitor-sensitive events of the replicative cycle in rat liver. Hepatocyte proliferation was induced by alpha-hexachlorocyclohexane and by partial hepatectomy; the onset of DNA synthesis and of mitotic activity were determined and used as reference points in the cell cycle. Inhibition of cell proliferation was achieved by CFT 1201, SKF 525-A, and actinomycin D. It was found that the inhibitory action of the three agents ends at the same stage of the replicative cycle, 0--2 h before the G1/S transition, in both alpha-hexachlorocyclohexane-stimulated and regenerating rat liver. It is concluded that the molecular events sensitive to CFT 1201, SKF 525-A or actinomycin D are either identical or temporally closely associated; they do not figure in the metabolic activation of alpha-hexachlorocyclohexane.

摘要

本研究旨在探讨大鼠肝脏复制周期中某些抑制剂敏感事件的性质、顺序和时间位置。用α-六氯环己烷和部分肝切除术诱导肝细胞增殖;确定DNA合成和有丝分裂活性的起始,并将其用作细胞周期中的参考点。用CFT 1201、SKF 525-A和放线菌素D抑制细胞增殖。结果发现,在α-六氯环己烷刺激的和再生的大鼠肝脏中,这三种药物的抑制作用均在复制周期的同一阶段结束,即G1/S转换前0-2小时。结论是,对CFT 1201、SKF 525-A或放线菌素D敏感的分子事件要么相同,要么在时间上紧密相关;它们在α-六氯环己烷的代谢活化中不起作用。

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