Serotonergic control of GABAergic inhibition in the lateral amygdala

Abstract

Much evidence implicates the serotonergic regulation of the amygdala in anxiety. Thus the present study was undertaken to characterize the influence of serotonin (5-HT) on principal neurons (PNs) of the rat lateral amygdala (LA), using whole cell recordings in vitro. Because inhibition is a major determinant of PN activity, we focused on the control of GABAergic transmission by 5-HT. IPSCs were elicited by local electrical stimulation of LA in the presence of glutamate receptor antagonists. We found that 5-HT reduces GABAAinhibitory postsynaptic currents (IPSCs) via presynaptic 5-HT1Breceptors. While the presynaptic inhibition of GABA release also attenuated GABABcurrents, this effect was less pronounced than for GABAAcurrents because 5-HT also induced a competing postsynaptic enhancement of GABABcurrents. That is, GABABcurrents elicited by pressure application of GABA or baclofen were enhanced by 5-HT. In addition, we obtained evidence suggesting that 5-HT differentially regulates distinct subsets of GABAergic synapses. Indeed, GABAAIPSCs were comprised of two components: a relatively 5-HT-insensitive IPSC that had a fast time course and a 5-HT-sensitive component that had a slower time course. Because the relative contribution of these two components varied depending on whether neurons were recorded at proximity versus at a distance from the stimulating electrodes, we speculate that distinct subtypes of local-circuit cells contribute the two contingents of GABAergic synapses. Overall, our results indicate that 5-HT is a potent regulator of synaptic inhibition in LA.NEW & NOTEWORTHY We report that 5-HT, acting via presynaptic 5-HT1Breceptors, attenuates GABAAIPSCs by reducing GABA release in the lateral amygdala (LA). In parallel, 5-HT enhances GABABcurrents postsynaptically, such that GABABinhibitory postsynaptic currents (IPSCs) are relatively preserved from the presynaptic inhibition of GABA release. We also found that the time course of 5-HT-sensitive and -insensitive GABAAIPSCs differ. Together, these results indicate that 5-HT is a potent regulator of synaptic inhibition in LA.