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Eur J Pharmacol ; 371(2-3): 213-26, 1999 Apr 29.
Article in English | MEDLINE | ID: mdl-10357259

ABSTRACT

Within the context of the discussion about rational polytherapy, we determined the effects of four anaesthetics on the binding of [3H]t-butylbicycloorthobenzoate ([3H]TBOB) to the GABA(A) receptor complex in the presence of several concentrations of GABA (gamma-aminobutyric acid), in order to build a molecular model that can describe and quantify the interactions between the compounds. The empirical isobole method revealed that GABA and the anaesthetics acted synergically in displacing [3H]TBOB. This synergy could be described by a simple molecular model in which both GABA and the anaesthetics displaced [3H]TBOB allosterically and in which GABA allosterically enhanced the binding of the anaesthetics. To get information about the interaction between GABA and anaesthetics, we used [3H]TBOB as a tracer ligand. The model indicated that GABA enhanced the affinity of thiopental 3.0-fold, propofol 5.0-fold, the neuroactive steroids Org 20599 3.5-fold and Org 20549 13-fold. Insight into the molecular mechanism and strength of these interactions can help clinicians to choose therapeutically optimal drug and dose combinations: a step towards rational polytherapy.


Subject(s)
Anesthetics, General/metabolism , Bridged Bicyclo Compounds, Heterocyclic/metabolism , Prosencephalon/metabolism , Receptors, GABA-A/metabolism , gamma-Aminobutyric Acid/metabolism , Allosteric Site , Animals , Dose-Response Relationship, Drug , Drug Interactions , In Vitro Techniques , Models, Molecular , Rats , Rats, Wistar
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