Titre du document / Document title

Influence of genuine kavapyrone enantiomers on the GABA_A binding site

Auteur(s) / Author(s)

BOONEN G. ⁽¹⁾ ; HÄBERLEIN H. ⁽¹⁾ ;

Affiliation(s) du ou des auteurs / Author(s) Affiliation(s)

⁽¹⁾ Department of Pharmaceutical Biology, Philipps-University, Marburg, ALLEMAGNE

Résumé / Abstract

The influence of kavapyrones from Piper methysticum Forst. on the GABA_A receptor was demonstrated using radioreceptor assays. Both the dienolide yangonin and the genuine enolide enantiomers (+)-kavain, (+)-dihydrokavain, (+)-methysticin, and (+)-dihydromethysticin enhanced the specific binding of [³H]bicuculline methochloride ([³H]BMC). The kavapyrones have been investigated at assay concentrations between 100 μM and 10nM. (+)-Kavain, (+)-methysticin and (+)-dihydromethysticin showed maximal enhancements of 18% to 28 % at a concentration of 0.1 μM. whereas a 100-fold concentration of (+)-dihydrokavain revealed a similar modulatory activity of 22%. In the presence of 1 μM yangonin an increase of about 21 % of the specific [³H]BMC binding was observed. Desmethoxyyangonin did not alter the binding behavior of the GABA_A-receptor. A structure comparison of desmethoxyyangonin and yangonin indicated that the aromatic methoxy group was of particular importance for the modulatory activity. In contrast, the substitution pattern of the aromatic ring did not influence the modulatory activity of the enolides in a decisive manner. A structure comparison of desmethoxyyangonin and (+)-kavain revealed that an angular lactone ring was an important structure requirement. Both the enolides and the dienolides did not inhibit the specific binding of [³H]flunitrazepam. Thus, the influence on the GABA_A receptor was not based upon an interaction of these kavapyrones with the benzodiazepine receptor.

Revue / Journal Title

Planta medica   ISSN 0032-0943   CODEN PLMEAA 

Source / Source

1998, vol. 64, n^o6, pp. 504-506 (16 ref.)

Langue / Language

Anglais

Editeur / Publisher

Thieme, Stuttgart, ALLEMAGNE  (1953) (Revue)

Mots-clés anglais / English Keywords

Plant origin ; Medicinal plant ; Enantiomer ; Biological activity ; Biological fixation ; Gabaergic receptor A ; In vitro ; Radioreceptor assay ; Pharmacognosy ; Piper ; Piperaceae ; Dicotyledones ; Angiospermae ; Spermatophyta ;

Mots-clés français / French Keywords

Origine végétale ; Plante médicinale ; Enantiomère ; Activité biologique ; Fixation biologique ; Récepteur gabaergique A ; In vitro ; Méthode radiorécepteur ; Pharmacognosie ; Kavapyrone ; Piper methysticum ; Piper ; Piperaceae ; Dicotyledones ; Angiospermae ; Spermatophyta ;

Mots-clés espagnols / Spanish Keywords

Origen vegetal ; Planta medicinal ; Enantiómero ; Actividad biológica ; Fijación biológica ; Receptor gabaminérgico A ; In vitro ; Método radiorreceptor ; Farmacognosia ; Piper ; Piperaceae ; Dicotyledones ; Angiospermae ; Spermatophyta ;

Localisation / Location

INIST-CNRS, Cote INIST : 9624, 35400007283972.0030