The Influence of AA29504 on GABA Receptor Ligand Binding Properties and Its Implications on Subtype Selectivity

The unique pharmacological properties of δ-containing γ-aminobutyric acid type A receptors (δ-GABARs) make them an attractive target for selective and persistent modulation of neuronal excitability. However, the availability of selective modulators targeting δ-GABARs remains limited. AA29504 ([2-amino-4-(2,4,6-trimethylbenzylamino)-phenyl]-carbamic acid ethyl ester), an analog of K channel opener retigabine, acts as an agonist and a positive allosteric modulator (Ago-PAM) of δ-GABARs. Based on electrophysiological studies using recombinant receptors, AA29504 was found to be a more potent and effective agonist in δ-GABARs than in γ2-GABARs. In comparison, AA29504 positively modulated the activity of recombinant δ-GABARs more effectively than γ2-GABARs, with no significant differences in potency. The impact of AA29504's efficacy- and potency-associated GABAR subtype selectivity on radioligand binding properties remain unexplored. Using [H]4'-ethynyl-4-n-propylbicycloorthobenzoate ([H]EBOB) binding assay, we found no difference in the modulatory potency of AA29504 on GABA- and THIP (4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol)-induced responses between native forebrain GABARs of wild type and δ knock-out mice. In recombinant receptors expressed in HEK293 cells, AA29504 showed higher efficacy on δ- than γ-GABARs in the GABA-independent displacement of [H]EBOB binding. Interestingly, AA29504 showed a concentration-dependent stimulation of [H]muscimol binding to γ-GABARs, which was absent in δ-GABARs. This was explained by AA29504 shifting the low-affinity γ-GABAR towards a higher affinity desensitized state, thereby rising new sites capable of binding GABAR agonists with low nanomolar affinity. Hence, the potential of AA29504 to act as a desensitization-modifying allosteric modulator of γ2-GABARs deserves further investigation for its promising influence on shaping efficacy, duration and plasticity of GABAR synaptic responses.