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[硫酸肼增强抗肿瘤药物疗效的机制]

[Mechanism of increasing the effect of antineoplastic agents by hydrazine sulfate].

作者信息

Tret'iakov A V, Filov V A

出版信息

Vopr Onkol. 1977;23(5):94-8.

PMID:407720
Abstract

The results of the in vivo and in vitro experiments indicated that hydrazine sulphate is a new potent inhibitor of the biotransformation of physiologically active compounds, including those with an antitumor effect. It is suggested that hydrazine sulphate renders an inhibitory effect by retarding the access of xenobiotics to microsomal enzymes active centers metabolizing them. The retardation of antitumor compounds biotransformation effected by hydrazine sulphate in vitro enabled the explanation of the enhanced effect of cytostatics, used in combination with hydrazine sulphate in vivo. This fact seems to speak in favour of the perspective clinical application of hydrazine sulphate for potentiation of the antitumor effect of cytostatics.

摘要

体内和体外实验结果表明,硫酸肼是生理活性化合物生物转化的新型强效抑制剂,包括具有抗肿瘤作用的化合物。有人认为,硫酸肼通过延缓外源性物质进入代谢它们的微粒体酶活性中心而发挥抑制作用。体外实验中硫酸肼对抗肿瘤化合物生物转化的延缓作用,解释了体内与硫酸肼联合使用时细胞抑制剂效果增强的原因。这一事实似乎支持硫酸肼在临床上用于增强细胞抑制剂抗肿瘤作用的前景。

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