Influence of subunit configuration on the interaction of picrotoxin-site ligands with recombinant GABA(A) receptors

We have assessed the interaction of picrotoxin and a putative picrotoxin-si te ligand [4-dimethyl-3-t-butylcarboxyl-3,5-dihydro (1,5-a) quinoxaline] (U -93631) with varying configurations of recombinant GABA(A) receptors, using the whole-cell patch clamp technique. In alpha 2 beta 2 gamma 2 GABA(A) re ceptors, coapplication of picrotoxin with GABA had minimal effects on initi al GABA-activated Cl- current amplitude, and subsequently enhanced decay of GABA-activated Cl- currents. The half-maximal inhibitory concentration (IC 50) for picrotoxin in alpha 2 beta 2 gamma 2 receptors was 10.3 +/- 1.6 mu M. The alpha subunit isoform did not affect picrotoxin-induced inhibition, as IC50 values for alpha 3 beta 2 gamma 2 (5.1 +/- 0.7 mu M) and alpha 6 be ta 2 gamma 2 receptors (7.2 +/- 0.4 mu M) were comparable to those obtained in alpha 2 beta 2 gamma 2 receptors. Interestingly, in receptors lacking a n alpha subunit (beta 2 gamma 2 configuration), picrotoxin had a markedly l ower IC50 (0.5 +/- 0.05 mu M) compared to alpha-containing receptors. The i nhibitory profile was generally similar for the presumed picrotoxin-site li gand U-93631, i.e., IC50 values were comparable in all alpha beta gamma-con taining receptors, but the IC50 in beta 2 gamma 2 receptors was greater tha n 10-fold lower. In addition, a modest but significant initial stimulation of GABA-activated current by U-93631 was observed in alpha 2 beta 2 gamma a nd beta 2 gamma 2 receptors. A mutation in the second transmembrane domain, shown previously to abolish picrotoxin sensitivity, also greatly attenuate d sensitivity to U-93631. Moreover, incubation of receptors with excess U-9 3631 hindered picrotoxin's ability to gain access to its binding site; both results indicate that U-93631 interacts at the picrotoxin site of the rece ptor. Our results indicate the presence of an alpha subunit hinders the abi lity of picrotoxin to block the GABA(A) receptor, and thus provides additio nal insight into the site of action of picrotoxin. In addition, we have sho wn that domains important for the actions of picrotoxin also affect U-93631 . Thus, this compound should prove to be a useful ligand for analysis of th e convulsant site of this receptor. (C) 2000 Published by Elsevier Science B.V. All rights reserved.