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Specific Subtypes of GABA_A Receptors Mediate Phasic and Tonic Forms of Inhibition in Hippocampal Pyramidal Neurons

University of Zurich, Institute of Pharmacology and Toxicology, Zurich, Switzerland

Submitted 10 November 2005; accepted in final form 8 May 2006

The main inhibitory neurotransmitter in the mammalian brain, GABA, mediates multiple forms of inhibitory signals, such as fast and slow inhibitory postsynaptic currents and tonic inhibition, by activating a diverse family of ionotropic GABA_A receptors (GABA_ARs). Here, we studied whether distinct GABA_AR subtypes mediate these various forms of inhibition using as approach mice carrying a point mutation in the -subunit rendering individual GABA_AR subtypes insensitive to diazepam without altering their GABA sensitivity and expression of receptors. Whole cell patch-clamp recordings were performed in hippocampal pyramidal cells from single, double, and triple mutant mice. Comparing diazepam effects in knock-in and wild-type mice allowed determining the contribution of 1, 2, 3, and 5 subunits containing GABA_ARs to phasic and tonic forms of inhibition. Fast phasic currents were mediated by synaptic 2-GABA_ARs on the soma and by synaptic 1-GABA_ARs on the dendrites. No contribution of 3- or 5-GABA_ARs was detectable. Slow phasic currents were produced by both synaptic and perisynaptic GABA_ARs, judged by their strong sensitivity to blockade of GABA reuptake. In the CA1 area, but not in the subiculum, perisynaptic 5-GABA_ARs contributed to slow phasic currents. In the CA1 area, the diazepam-sensitive component of tonic inhibition also involved activation of 5-GABA_ARs and slow phasic and tonic signals shared overlapping pools of receptors. These results show that the major forms of inhibitory neurotransmission in hippocampal pyramidal cells are mediated by distinct GABA_ARs subtypes.

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