RT Journal Article
SR Electronic
T1 Positive Allosteric Modulation of Native and Recombinant  γ-Aminobutyric Acid<sub>B</sub> Receptors by 2,6-Di-<em>tert</em>-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol (CGP7930) and its Aldehyde Analog CGP13501
JF Molecular Pharmacology
JO Mol Pharmacol
FD American Society for Pharmacology and Experimental Therapeutics
SP 963
OP 971
DO 10.1124/mol.60.5.963
VO 60
IS 5
A1 Stephan Urwyler
A1 Johannes Mosbacher
A1 Kurt Lingenhoehl
A1 Jakob Heid
A1 Karin Hofstetter
A1 Wolfgang Froestl
A1 Bernhard Bettler
A1 Klemens Kaupmann
YR 2001
UL http://molpharm.aspetjournals.org/content/60/5/963.abstract
AB The compounds CGP7930 [2,6-Di-tert-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol] and its close analog CGP13501 were identified as positive modulators of γ-aminobutyric acidB (GABAB) receptor function. They potentiate GABA-stimulated guanosine 5′-O-(3-[35S]thiotriphosphate) (GTPγ[35S]) binding to membranes from a GABAB(1b/2) expressing Chinese hamster ovary (CHO) cell line at low micromolar concentrations and are ineffective in the absence of GABA. The structurally related compounds propofol and malonoben are inactive. Similar effects of CGP7930 are seen in a GTPγ[35S] binding assay using a native GABAB receptor preparation (rat brain membranes). Receptor selectivity is demonstrated because no modulation of glutamate-induced GTPγ[35S] binding is seen in a CHO cell line expressing the metabotropic glutamate receptor subtype 2. Dose-response curves with GABA in the presence of different fixed concentrations of CGP7930 reveal an increase of both the potency and maximal efficacy of GABA at the GABAB(1b/2) heteromer. Radioligand binding studies show that CGP7930 increases the affinity of agonists but acts at a site different from the agonist binding site. Agonist affinity is not modulated by CGP7930 at homomeric GABAB(1b) receptors. In addition to GTPγ[35S] binding, we show that CGP7930 also has modulatory effects in cellular assays such as GABAB receptor-mediated activation of inwardly rectifying potassium channels in Xenopus laevis oocytes and Ca2+ signaling in human embryonic kidney 293 cells. Furthermore, we show that CGP7930 enhances the inhibitory effect ofl-baclofen on the oscillatory activity of cultured cortical neurons. This first demonstration of positive allosteric modulation at GABAB receptors may represent a novel means of therapeutic interference with the GABA-ergic system.