二甲双胍
有机阳离子转运蛋白
药代动力学
内分泌学
内科学
摄入
药理学
葡萄糖转运蛋白
化学
医学
运输机
剂量-反应关系
糖尿病
胰岛素
生物化学
基因
作者
Steve K. Cho,J S Yoon,Min Goo Lee,Dong Hwan Lee,L A Lim,Kyong Park,Min Soo Park,Jae‐Yong Chung
标识
DOI:10.1038/clpt.2010.266
摘要
We evaluated the effect of the pregnane X receptor (PXR) agonist rifampin on metformin pharmacokinetics, organic cation transporter 1 (OCT1) and OCT2 mRNA levels, and glucose levels, using the oral glucose tolerance test (OGTT) in 16 healthy subjects. The glucose-lowering effects of metformin were evaluated by OGTT before and after metformin treatment on days 1 and 2 and again on days 13 and 14 after a 10-day course of rifampin. Rifampin increased the difference in maximum glucose levels (ΔGmax) by 41.9% (P = 0.024) and the area under the concentration–time curve (AUC) during the first 60 min after glucose ingestion (ΔAUCgluc60) by 54.5% (P = 0.020). Renal clearance (CLR) of metformin was increased by 16% (P = 0.008), but the systemic exposure was only slightly increased (13%, P = 0.049), possibly because of increased absorption. Rifampin increased OCT1 mRNA levels 4.1-fold in peripheral blood cells (P = 0.001); however, OCT2 mRNA was not detected. Our results suggest that rifampin increases OCT1 expression and hepatic uptake of metformin, leading to enhanced glucose-lowering action. Clinical Pharmacology & Therapeutics (2011) 89 3, 416–421. doi:10.1038/clpt.2010.266
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