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Characterization of ( R , S )‐5,7‐di‐ tert ‐butyl‐3‐hydroxy‐3‐trifluoromethyl‐3 H ‐benzofuran‐2‐one as a positive allosteric modulator of GABA B receptors
Author(s) -
Malherbe P,
Masciadri R,
Norcross R D,
Knoflach F,
Kratzeisen C,
Zenner MT,
Kolb Y,
Marcuz A,
Huwyler J,
Nakagawa T,
Porter R H P,
Thomas A W,
Wettstein J G,
Sleight A J,
Spooren W,
Prinssen E P
Publication year - 2008
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/bjp.2008.135
Subject(s) - baclofen , allosteric modulator , gabab receptor , chemistry , pharmacology , allosteric regulation , receptor , in vivo , gabaa receptor , population , agonist , biology , biochemistry , medicine , microbiology and biotechnology , environmental health
Background and purpose: As baclofen is active in patients with anxiety disorders, GABA B receptors have been implicated in the modulation of anxiety. To avoid the side effects of baclofen, allosteric enhancers of GABA B receptors have been studied to provide an alternative therapeutic avenue for modulation of GABA B receptors. The aim of this study was to characterize derivatives of ( R , S )‐5,7‐di‐ tert ‐butyl‐3‐hydroxy‐3‐trifluoromethyl‐3 H ‐benzofuran‐2‐one ( rac ‐BHFF) as enhancers of GABA B receptors. Experimental approach: Enhancing properties of rac ‐BHFF were assessed in the Chinese hamster ovary (CHO)‐Gα16‐hGABA B(1a,2a) cells by Fluorometric Imaging Plate Reader and GTPγ[ 35 S]‐binding assays, and in rat hippocampal slices by population spike (PS) recordings. In vivo activities of rac ‐BHFF were assessed using the loss of righting reflex (LRR) and stress‐induced hyperthermia (SIH) models. Key results: In GTPγ[ 35 S]‐binding assays, 0.3 μ M rac ‐BHFF or its pure enantiomer (+)‐BHFF shifted the GABA concentration–response curve to the left, an effect that resulted in a large increase in both GABA potency (by 15.3‐ and 87.3‐fold) and efficacy (149% and 181%), respectively. In hippocampal slices, rac ‐BHFF enhanced baclofen‐induced inhibition of PS of CA1 pyramidal cells. In an in vivo mechanism‐based model in mice, rac ‐BHFF increased dose‐dependently the LRR induced by baclofen with a minimum effective dose of 3 mg kg −1 p.o. rac ‐BHFF (100 mg kg −1 p.o.) tested alone had no effect on LRR nor on spontaneous locomotor activity, but exhibited anxiolytic‐like activity in the SIH model in mice. Conclusions and implications: rac ‐BHFF derivatives may serve as valuable pharmacological tools to elucidate the pathophysiological roles played by GABA B receptors in the central and peripheral nervous systems. British Journal of Pharmacology (2008) 154 , 797–811; doi: 10.1038/bjp.2008.135 ; published online 21 April 2008