首页 | 本学科首页   官方微博 | 高级检索  
     


Itraconazole,gemfibrozil and their combination markedly raise the plasma concentrations of loperamide
Authors:Mikko?Niemi  author-information"  >  author-information__contact u-icon-before"  >  mailto:mikko.niemi@hus.fi"   title="  mikko.niemi@hus.fi"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Aleksi?Tornio,Marja?K.?Pasanen,Hanna?Fredrikson,Pertti?J.?Neuvonen,Janne?T.?Backman
Affiliation:(1) Department of Clinical Pharmacology, Helsinki University Central Hospital, P.O. Box 340, FI-00029 HUS, Finland
Abstract:Objective Loperamide is biotransformed in vitro by the cytochromes P450 (CYP) 2C8 and 3A4 and is a substrate of the P-glycoprotein efflux transporter. Our aim was to investigate the effects of itraconazole, an inhibitor of CYP3A4 and P-glycoprotein, and gemfibrozil, an inhibitor of CYP2C8, on the pharmacokinetics of loperamide.Methods In a randomized crossover study with 4 phases, 12 healthy volunteers took 100 mg itraconazole (first dose 200 mg), 600 mg gemfibrozil, both itraconazole and gemfibrozil, or placebo, twice daily for 5 days. On day 3, they ingested a single 4-mg dose of loperamide. Loperamide and N-desmethylloperamide concentrations in plasma were measured for up to 72 h and in urine for up to 48 h. Possible central nervous system effects of loperamide were assessed by the Digit Symbol Substitution Test and by subjective drowsiness.Results Itraconazole raised the peak plasma loperamide concentration (Cmax) 2.9-fold (range, 1.2–5.0; P<0.001) and the total area under the plasma loperamide concentration-time curve (AUC0-∞) 3.8-fold (1.4–6.6; P<0.001) and prolonged the elimination half-life (t½) of loperamide from 11.9 to 18.7 h (P<0.001). Gemfibrozil raised the Cmax of loperamide 1.6-fold (0.9–3.2; P<0.05) and its AUC0-∞ 2.2-fold (1.0–3.7; P<0.05) and prolonged its t½ to 16.7 h (P<0.01). The combination of itraconazole and gemfibrozil raised the Cmax of loperamide 4.2-fold (1.5–8.7; P<0.001) and its AUC0-∞ 12.6-fold (4.3–21.8; P<0.001) and prolonged the t½ of loperamide to 36.9 h (P<0.001). The amount of loperamide excreted into urine within 48 h was increased 3.0-fold, 1.4-fold and 5.3-fold by itraconazole, gemfibrozil and their combination, respectively (P<0.05). Itraconazole, gemfibrozil and their combination reduced the plasma AUC0–72 ratio of N-desmethylloperamide to loperamide by 65%, 46% and 88%, respectively (P<0.001). No significant differences were seen in the Digit Symbol Substitution Test or subjective drowsiness between the phases.Conclusion Itraconazole, gemfibrozil and their combination markedly raise the plasma concentrations of loperamide. Although not seen in the psychomotor tests used, an increased risk of adverse effects should be considered during concomitant use of loperamide with itraconazole, gemfibrozil and especially their combination.
Keywords:CYP2C8  CYP3A4  Gemfibrozil  Itraconazole  Loperamide  Pharmacokinetics
本文献已被 PubMed SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号