Agents that antagonize the action of GABA on ionotropic receptors are widely used to probe the function of this neurotransmiter. Three such agents are in common use: bicuculline, gabazine, and picrotoxinin. These three agents produce convulsions on systemic administration but act in signiicantly diferent ways. Bicuculline is a competitive antagonist of GABA A receptors. Gabazine is also a competitive antagonist of GABA A receptors, interacting with diferent residues on the receptors. Picrotoxinin is a noncompetitive antagonist acting on the chloride channel of GABA A and several other ionotropic CYSloop receptors including glycine, GABA C , and 5-HT 3 receptors. Many other structurally diverse agents are now known to act as GABA receptor antagonists, providing opportunities for the discovery of agents with selectivity for the myriad of ionotropic GABA receptors. TPMPA is a selective antagonist for GABA C receptors, which are insensitive to bicuculline. Like TPMPA, many antagonists of ionotropic GABA receptors are not convulsants, indicating that there is still much to be learnt about GABA function in the brain from the study of such agents and their possible therapeutic uses. The most recently discovered GABA A receptor nonconvulsive antagonist is S44819, which is subtype selective for α5-containing receptors, and is arousing much interest in relation to cognition.