6533b838fe1ef96bd12a4f0d

RESEARCH PRODUCT

Effects of caffeine intake on the pharmacokinetics of melatonin, a probe drug for CYP1A2 activity

Anna NordmarkSebastian HärtterKari LaineGunnel TybringLeif BertilssonDirk-matthias Rose

subject

PharmacologyChemistryCYP1A2CmaxPharmacologyCrossover studyBioavailabilityMelatoninchemistry.chemical_compoundPharmacokineticsmedicinePharmacology (medical)CaffeineParaxanthinemedicine.drug

description

Aims  The aim of this study was to assess the influence of concomitant caffeine intake on the pharmacokinetics of oral melatonin, a probe drug for CYP1A2 activity. Methods  Twelve healthy subjects, six smokers and six nonsmokers, were given melatonin (6 mg) either alone or in combination with caffeine (3 × 200 mg). Blood samples for the analysis of melatonin or caffeine and paraxanthine were taken from 1 h before until 6 h after intake of melatonin. Subjects were genotyped with respect to the CYP1A2*1F (C734A) polymorphism. Results  When caffeine was coadministered the Cmax and AUC of melatonin were increased on average by 142% (P = 0.001, confidence interval on the difference 44, 80%) and 120% (P < 0.001, confidence interval on the difference 63, 178%), respectively. The inhibitory effect of caffeine was more pronounced in nonsmokers and in individuals with the *1F/*1F genotype. Conclusion  The results of this study revealed a pronounced effect of caffeine on the bioavailability of orally given melatonin, most probably due to inhibition of CYP1A2 activity.

https://doi.org/10.1046/j.1365-2125.2003.01933.x