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薄荷醇对健康女性志愿者咖啡因代谢及药效学的影响。

Influence of menthol on caffeine disposition and pharmacodynamics in healthy female volunteers.

作者信息

Gelal Ayse, Guven Hulya, Balkan Dilara, Artok Levent, Benowitz Neal L

机构信息

Associated Professor in Pharmacology, Dokuz Eylul University Medical Faculty, Department of Pharmacology, Inciralti, 35340 Izmir, Turkey.

出版信息

Eur J Clin Pharmacol. 2003 Sep;59(5-6):417-22. doi: 10.1007/s00228-003-0631-1. Epub 2003 Aug 14.

Abstract

OBJECTIVES

The present study was undertaken to determine whether a single oral dose of menthol affects the metabolism of caffeine, a cytochrome P(450) 1A2 (CYP1A2) substrate, and pharmacological responses to caffeine in people.

METHODS

Eleven healthy female subjects participated in a randomized, double-blind, two-way crossover study, comparing the kinetics and effects of a single oral dose of caffeine (200 mg) in coffee taken together with a single oral dose of menthol (100 mg) or placebo capsules. Serum caffeine concentrations and cardiovascular and subjective parameters were measured throughout the study.

RESULTS

Co-administration of menthol resulted in an increase of caffeine t(max) values from 43.6+/-20.6 min (mean+/-SD) to 76.4+/-28.0 min ( P<0.05). The C(max) values of caffeine were lower in the menthol phase than in the placebo phase, but this effect was not statistically significant ( P=0.06). (AUC)(0-24), (AUC)(0- infinity ), terminal half-life and oral clearance were not affected by menthol. Only nine subjects' cardiovascular data were included in the analysis because of technical problems during the measurements. After caffeine, heart rate decreased in both treatment phases. The maximum decrease in heart rate was less in the menthol phase (-8.9+/-3.9 beats/min) than in the placebo phase (-13.1+/-2.1 beats/min) ( P=0.024). There were no statistically significant differences in systolic and diastolic blood pressures between the two treatments.

CONCLUSIONS

We conclude that a single oral dose of pure menthol (100 mg) delays caffeine absorption and blunts the heart-rate slowing effect of caffeine, but does not affect caffeine metabolism. The possibility that menthol slows the absorption of other drugs should be considered.

摘要

目的

本研究旨在确定单次口服薄荷醇是否会影响咖啡因(一种细胞色素P450 1A2(CYP1A2)底物)的代谢以及人体对咖啡因的药理反应。

方法

11名健康女性受试者参与了一项随机、双盲、双向交叉研究,比较单次口服含200毫克咖啡因的咖啡与单次口服100毫克薄荷醇胶囊或安慰剂胶囊时咖啡因的动力学和效应。在整个研究过程中测量血清咖啡因浓度以及心血管和主观参数。

结果

薄荷醇与咖啡因合用时,咖啡因的t(max)值从43.6±20.6分钟(均值±标准差)增加至76.4±28.0分钟(P<0.05)。薄荷醇阶段咖啡因的C(max)值低于安慰剂阶段,但此效应无统计学意义(P=0.06)。(AUC)(0 - 24)、(AUC)(0 - ∞)、终末半衰期和口服清除率不受薄荷醇影响。由于测量过程中的技术问题,分析中仅纳入了9名受试者的心血管数据。服用咖啡因后,两个治疗阶段的心率均下降。薄荷醇阶段心率的最大降幅(-8.9±3.9次/分钟)小于安慰剂阶段(-13.1±2.1次/分钟)(P=0.024)。两种治疗之间的收缩压和舒张压无统计学显著差异。

结论

我们得出结论,单次口服100毫克纯薄荷醇会延迟咖啡因吸收并减弱咖啡因的心率减慢效应,但不影响咖啡因代谢。应考虑薄荷醇减缓其他药物吸收的可能性。

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