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8-甲氧基补骨脂素与甲苯磺丁脲体内外相互作用的研究。

Studies on 8-methoxypsoralen tolbutamide interactions in vitro and in vivo.

作者信息

Bevilacqua R, Baccichetti F, Gaion R M

机构信息

Dipartimento di Scienze Farmaceutiche, Università di Padova, Italy.

出版信息

Farmaco. 1991 Apr;46(4):579-92.

PMID:1930554
Abstract

The present study aimed at characterizing the influence of tolbutamide on the distribution of 8-methoxypsoralen (8-MOP) in mouse serum and organs. Experiments performed in vitro clearly showed that tolbutamide causes competitive displacement of 8-MOP from its binding sites on human serum albumin. Similarly, the amount of labelled compound(s) bound in serum after oral administration of 3H-8-MOP to mice was significantly reduced when tolbutamide was given by the same route. The quantitative distribution of radioactivity from 3H-8-MOP in mouse tissues varied according to organ (liver, intestine, skin, etc.,), and was maximum in the organs of elimination. In all the organs studied, the administration of tolbutamide 2 hours after that of 3H-8-MOP caused a dose-dependent reduction of the radioactive compound(s) present in tissues, suggesting that tolbutamide may accelerate the excretion of 8-MOP and/or its metabolites from the body.

摘要

本研究旨在表征甲苯磺丁脲对8-甲氧基补骨脂素(8-MOP)在小鼠血清和器官中分布的影响。体外实验清楚地表明,甲苯磺丁脲会导致8-MOP从其在人血清白蛋白上的结合位点发生竞争性置换。同样,当以相同途径给小鼠口服3H-8-MOP后,甲苯磺丁脲经相同途径给药时,血清中结合的标记化合物量显著减少。3H-8-MOP在小鼠组织中的放射性定量分布因器官(肝脏、肠道、皮肤等)而异,在排泄器官中最高。在所有研究的器官中,在给予3H-8-MOP 2小时后给予甲苯磺丁脲会导致组织中存在的放射性化合物剂量依赖性减少,这表明甲苯磺丁脲可能会加速8-MOP及其代谢产物从体内的排泄。

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