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在健康受试者中,口服药物(对乙酰氨基酚)在与皮下注射艾塞那肽(艾塞那肽-4)不同时间给药时的药代动力学。

Pharmacokinetics of an oral drug (acetaminophen) administered at various times in relation to subcutaneous injection of exenatide (exendin-4) in healthy subjects.

作者信息

Blase Erich, Taylor Kristin, Gao Hong-Ye, Wintle Matthew, Fineman Mark

机构信息

Amylin Pharmaceuticals Inc, 9360 Towne Centre Drive, Suite 110, San Diego, CA 92121, USA.

出版信息

J Clin Pharmacol. 2005 May;45(5):570-7. doi: 10.1177/0091270004274432.

Abstract

Exenatide is an incretin mimetic with potential glucoregulatory activity in type 2 diabetes. This randomized, single-blind, placebo-controlled 6-way crossover study assessed exenatide's effect on acetaminophen pharmacokinetics. Of 40 randomized healthy subjects, 39 completed the study. On the placebo day, acetaminophen (1000 mg) was ingested and placebo injected subcutaneously at 0 hours. On exenatide days, acetaminophen was ingested at -1, 0, +1, +2, and +4 hours, relative to the 10 mug exenatide injected subcutaneously at 0 hours. With exenatide injection, mean plasma acetaminophen AUC(0-12 h) values were reduced by 11% to 24% (vs placebo). Peak plasma acetaminophen concentrations were similar for the -1-hour and placebo groups and reduced by 37% to 56% at other times. The most frequent adverse events were generally mild to moderate nausea and vomiting. Exenatide treatment concurrent with or preceding acetaminophen ingestion slowed acetaminophen absorption but had minimal effect on the extent of absorption.

摘要

艾塞那肽是一种肠促胰岛素类似物,对2型糖尿病具有潜在的血糖调节活性。这项随机、单盲、安慰剂对照的6交叉试验评估了艾塞那肽对乙酰氨基酚药代动力学的影响。40名随机入组的健康受试者中,39人完成了研究。在安慰剂日,受试者于0小时口服1000mg乙酰氨基酚,并皮下注射安慰剂。在艾塞那肽日,相对于0小时皮下注射的10μg艾塞那肽,受试者于-1、0、+1、+2和+4小时口服乙酰氨基酚。注射艾塞那肽后,乙酰氨基酚的平均血浆AUC(0-12小时)值降低了11%至24%(与安慰剂相比)。-1小时组和安慰剂组的血浆乙酰氨基酚峰值浓度相似,其他时间降低了37%至56%。最常见的不良事件一般为轻至中度恶心和呕吐。与摄入乙酰氨基酚同时或之前进行艾塞那肽治疗会减慢乙酰氨基酚的吸收,但对吸收程度影响极小。

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