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Interaction of licorice on glycyrrhizin pharmacokinetics.

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 biol...

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Autores principales: Cantelli-Forti, G, Maffei, F, Hrelia, P, Bugamelli, F, Bernardi, M, D'Intino, P, Maranesi, M, Raggi, M A
Formato: Texto
Lenguaje:English
Publicado: 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566785/
https://www.ncbi.nlm.nih.gov/pubmed/7698088
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author Cantelli-Forti, G
Maffei, F
Hrelia, P
Bugamelli, F
Bernardi, M
D'Intino, P
Maranesi, M
Raggi, M A
author_facet Cantelli-Forti, G
Maffei, F
Hrelia, P
Bugamelli, F
Bernardi, M
D'Intino, P
Maranesi, M
Raggi, M A
author_sort Cantelli-Forti, G
collection PubMed
description 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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spelling pubmed-15667852006-09-19 Interaction of licorice on glycyrrhizin pharmacokinetics. Cantelli-Forti, G Maffei, F Hrelia, P Bugamelli, F Bernardi, M D'Intino, P Maranesi, M Raggi, M A Environ Health Perspect Research Article 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. 1994-11 /pmc/articles/PMC1566785/ /pubmed/7698088 Text en
spellingShingle Research Article
Cantelli-Forti, G
Maffei, F
Hrelia, P
Bugamelli, F
Bernardi, M
D'Intino, P
Maranesi, M
Raggi, M A
Interaction of licorice on glycyrrhizin pharmacokinetics.
title Interaction of licorice on glycyrrhizin pharmacokinetics.
title_full Interaction of licorice on glycyrrhizin pharmacokinetics.
title_fullStr Interaction of licorice on glycyrrhizin pharmacokinetics.
title_full_unstemmed Interaction of licorice on glycyrrhizin pharmacokinetics.
title_short Interaction of licorice on glycyrrhizin pharmacokinetics.
title_sort interaction of licorice on glycyrrhizin pharmacokinetics.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566785/
https://www.ncbi.nlm.nih.gov/pubmed/7698088
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