Interaction of licorice on glycyrrhizin pharmacokinetics.
Author(s) -
Giorgio CantelliForti,
Francesca Maffei,
Patrizia Hrelia,
Francesca Bugamelli,
M. De Bernardi,
Paola E. D'Intino,
Margherita Maranesi,
Maria Augusta Raggi
Publication year - 1994
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.94102s965
Subject(s) - glycyrrhizin , pharmacokinetics , bioavailability , cmax , pharmacology , oral administration , chemistry , absorption (acoustics) , high performance liquid chromatography , plasma concentration , urine , area under the curve , chromatography , medicine , biochemistry , physics , acoustics
The effects of components of aqueous licorice root extract (LE) on the pharmacokinetics of glycyrrhizin (G) and glycyrrhetic acid (GA) were investigated in rats and humans. The aim of this work was to define the role of pharmacokinetics in G toxicity. In the procedure, G and GA were detected in biological fluids by means of recently improved HPLC methods. Significantly lower G and GA plasma levels were found in rats and humans treated with LE compared to the levels obtained with those in which G alone was administered. The pharmacokinetic curves showed significant differences in the areas under the plasma-time curve (AUC), Cmax, and Tmax parameters. The data obtained from urine samples are in agreement with the above results and confirm a reduced bioavailability of G present in LE compared to pure G. This should be attributed to the interaction during intestinal absorption between the G constituent and the several components in LE. The modified bioavailability could explain the various clinical adverse effects resulting from the chronic oral administration of G alone as opposed to LE.
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