U-93631 CAUSES RAPID DECAY OF GAMMA-AMINOBUTYRIC ACID-INDUCED CHLORIDE CURRENTS IN RECOMBINANT RAT GAMMA-AMINOBUTYRIC-ACID TYPE-A RECEPTORS

We discovered the ability of U-93631 tylcar-boxyl-4,5-dihydro[1,5-a]im idazoquinoxaline) to accelerate decay of gamma-aminobutyric acid (GABA )-induced currents, and we explored its mechanism in human embryonic k idney cells (HEK-293) stably expressing the alpha1beta2gamma2 subtype of GABA(A) receptors. Inward currents (Cl- efflux) induced by 5 mum GA BA at the holding potential of -60 mV (under a symmetrical Cl- gradien t) decayed with an exponential time course with a mean time constant ( T) of 222 +/- 25 sec, as examined with the whole-cell configuration of the patch-clamp technique. The monoexponential decay was greatly acce lerated in the presence of U-93631 at 5 mum, with the mean tau value b eing 5.2 +/- 0.5 sec. The 7 values were dependent on the concentration of U-93631, with an estimated K(d) of approximately 2 mum. Outward cu rrents at the holding potential of +60 mV decayed with a similar tau v alue in the presence of the drug, suggesting the voltage independence of the drug action. The initial amplitude of the GABA (5 mum)-induced Cl- current was not affected by preincubation with U-93631 (5 mum) or GABA (200 nm) alone but was reduced by preincubation with the combinat ion of the two. In the presence of U-93631 at 5 mum, the peak amplitud e decreased as a function of GABA concentration, with the half-maximal inhibitory concentration being approximately 100 nm, which is close t o the K(d) for the high affinity GABA site (85 nm). It appears that th e drug interacts with GABA-bound receptors (at least monoliganded) and accelerates receptor desensitization, rather than acting as an open c hannel blocker. The binding site for U-93631 on GABA(A) receptors seem s not to overlap with GABA, barbiturate, or benzodiazepine sites, beca use the drug effect persisted in the presence of excess ligands for th ose sites. With cloned GABA(A) receptors composed of only alpha1beta2, beta2gamma2, or alpha1gamma2 subunits, U-93631 also accelerated the d ecay rate. This lack of subtype selectivity raises the possibility tha t the compound interacts with a region common among the three subunits , probably a novel modulatory site, which can possibly be exploited as a novel therapeutic target.