Faculty Scholarship (PHRM)
 

Title

alpha 7 nicotinic acetylcholine receptors on GABAergic interneurons evoke dendritic and somatic inhibition of hippocampal neurons.

Document Type

Article

Publication/Creation/Presentation Date

2002

Keywords

neurons, ecetylcholine, hippocampus

Journal

Journal of Neurophysiology

Volume

87

Disciplines

Molecular and Cellular Neuroscience | Pharmacy and Pharmaceutical Sciences | Systems Neuroscience

Abstract

GABAergic interneurons in the hippocampus express high levels of α7 nicotinic acetylcholine receptors, but because of the diverse roles played by hippocampal interneurons, the impact of activation of these receptors on hippocampal output neurons (i.e., CA1 pyramidal cells) is unclear. Activation of hippocampal interneurons could directly inhibit pyramidal neuron activity but could also produce inhibition of other GABAergic cells leading to disinhibition of pyramidal cells. To characterize the inhibitory circuits activated by these receptors, exogenous acetylcholine was applied directly to CA1 interneurons in hippocampal slices, and the resulting postsynaptic responses were recorded from pyramidal neurons or interneurons. Inhibitory currents mediated by GABAA receptors were observed in 27/131 interneuron/pyramidal cell pairs, but no instances of disinhibition of spontaneous inhibitory events or GABAB receptor-mediated responses were observed. Two populations of bicuculline- sensitive GABAA receptor-mediated currents could be distinguished based on their kinetics and amplitude. Anatomical reconstructions of the interneurons in a subset of connected pairs support the hypothesis that these two populations correspond to inhibitory synapses located either on the somata or dendrites of pyramidal cells. In 11 interneuron/interneuron cell pairs, one presynaptic neuron was observed that produced strong inhibitory currents in several nearby interneurons, suggesting that disinhibition of pyramidal neurons may also occur. All three types of inhibitory responses (somatic-pyramidal, dendritic-pyramidal, and interneuronal) were blocked by the α7 receptor- selective antagonist methyllycaconitine. These data suggest activation of these functionally distinct circuits by α7 receptors results in significant inhibition of both hippocampal pyramidal neurons as well as interneurons.

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