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氨鲁米特对乳腺癌患者安替比林、茶碱和地高辛处置的影响。

Effect of aminoglutethimide on antipyrine, theophylline, and digitoxin disposition in breast cancer.

作者信息

Lønning E, Kvinnsland S, Bakke O M

出版信息

Clin Pharmacol Ther. 1984 Dec;36(6):796-802. doi: 10.1038/clpt.1984.259.

Abstract

The influence of aminoglutethimide (AG) on antipyrine, theophylline, and digitoxin kinetics was examined. Antipyrine was given as a single test dose before and after 3 mo of AG treatment, whereas theophylline and digitoxin kinetics were investigated at steady state in patients receiving these drugs therapeutically before and after AG therapy. During AG treatment, mean clearance rates for antipyrine, theophylline, and digitoxin increased by 81%, 32%, and 109%. Together with earlier reports of effects of AG on warfarin and dexamethasone disposition and on its own metabolism, these findings indicate that AG is a potent inducer of drug metabolizing microsomal monooxygenases of the liver. Since many drugs known to be metabolized by this enzyme system are frequently used for concomitant conditions in patients with breast cancer, interactions with AG are to be expected.

摘要

研究了氨鲁米特(AG)对安替比林、茶碱和地高辛药代动力学的影响。在AG治疗3个月前后分别给予安替比林单次试验剂量,而在接受这些药物治疗的患者中,在AG治疗前后研究了茶碱和地高辛在稳态时的药代动力学。在AG治疗期间,安替比林、茶碱和地高辛的平均清除率分别提高了81%、32%和109%。连同早期关于AG对华法林和地塞米松处置及其自身代谢影响的报道,这些发现表明AG是肝脏药物代谢微粒体单加氧酶的强效诱导剂。由于许多已知经该酶系统代谢的药物常用于乳腺癌患者的伴随病症,因此预计会与AG发生相互作用。

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