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茶碱代谢研究:安替比林的自身诱导及抑制作用

Studies on theophylline metabolism: autoinduction and inhibition by antipyrine.

作者信息

Denlinger C L, Stryker K K, Slusher L B, Vesell E S

出版信息

Clin Pharmacol Ther. 1987 May;41(5):522-30. doi: 10.1038/clpt.1987.67.

Abstract

Theophylline metabolism was accelerated in 11 of 13 normal male volunteers who received theophylline for 1 week in usual therapeutic doses (3 mg/kg orally t.i.d.). Mean theophylline clearance increased 24% and mean salivary elimination half-life (t1/2) decreased 16%, whereas the mean apparent volume of distribution of theophylline was unchanged at 0.7 L/kg. Large variations occurred in the extent of autoinduction, ranging from no change in two subjects to doubling of theophylline clearance in two others. Subjects who accelerated their theophylline metabolism exhibited a high inverse correlation between the extent of their induction and their two control values for theophylline clearance (r = -0.88 and -0.91; P less than 0.05). A single oral dose of antipyrine (18 mg/kg) simultaneously coadministered with a single oral dose of theophylline (5 mg/kg) retarded the metabolism of both theophylline and antipyrine. No significant change occurred in the apparent volume of distribution of either drug. Coadministration with antipyrine reduced mean theophylline clearance 18% and increased salivary t1/2 39%. Theophylline decreased mean antipyrine clearance 21% and increased its mean salivary t1/2 28%. Theophylline metabolism, therefore, is sensitive to not only autoinduction when theophylline is given long term at usual therapeutic doses but also inhibition when theophylline is coadministered with certain drugs.

摘要

13名正常男性志愿者接受常规治疗剂量(3mg/kg,口服,每日3次)的茶碱治疗1周后,其中11人的茶碱代谢加快。茶碱的平均清除率增加了24%,唾液消除半衰期(t1/2)平均缩短了16%,而茶碱的平均表观分布容积保持不变,为0.7L/kg。自身诱导程度存在很大差异,从2名受试者无变化到另外2名受试者的茶碱清除率增加一倍。茶碱代谢加快的受试者,其诱导程度与茶碱清除率的两个对照值之间呈现高度负相关(r = -0.88和-0.91;P<0.05)。单剂量口服安替比林(18mg/kg)与单剂量口服茶碱(5mg/kg)同时给药,会延缓茶碱和安替比林的代谢。两种药物的表观分布容积均未发生显著变化。与安替比林合用时,茶碱的平均清除率降低18%,唾液t1/2增加39%。茶碱使安替比林的平均清除率降低21%,唾液t1/2平均增加28%。因此,茶碱代谢不仅在长期给予常规治疗剂量时对自身诱导敏感,在与某些药物合用时对抑制作用也敏感。

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