Control of contextual memory through interneuronal α5-GABAA receptors

Author:

Zhu Mengwen1ORCID,Abdulzahir Alifayaz1,Perkins Mark G1,Chu Chan C12,Krause Bryan M1ORCID,Casey Cameron1ORCID,Lennertz Richard1,Ruhl David34,Hentschke Harald5ORCID,Nagarajan Rajasekar6,Chapman Edwin R3ORCID,Rudolph Uwe67ORCID,Fanselow Michael S89ORCID,Pearce Robert A1ORCID

Affiliation:

1. Department of Anesthesiology, University of Wisconsin-Madison , Madison, WI 53705 , USA

2. Lawrence University Present address: , Appleton, WI 54911 , USA

3. Department of Neuroscience, University of Wisconsin-Madison , Madison, WI 53705 , USA

4. Neurocrine Biosciences Present address: , San Diego, CA 92130 , USA

5. Freelance Data Scientist , Berlin 12555 , Germany

6. Department of Comparative Biosciences, University of Illinois at Urbana-Champaign , Urbana, IL 61802 , USA

7. Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign , Urbana, IL 61802 , USA

8. Department of Psychology, University of California, Los Angeles , Los Angeles, CA 61801 , USA

9. Department of Psychiatry, University of California, Los Angeles , Los Angeles, CA 90095 , USA

Abstract

Abstract γ-Aminobutyric acid type A receptors that incorporate α5 subunits (α5-GABAARs) are highly enriched in the hippocampus and are strongly implicated in control of learning and memory. Receptors located on pyramidal neuron dendrites have long been considered responsible, but here we report that mice in which α5-GABAARs have been eliminated from pyramidal neurons (α5-pyr-KO) continue to form strong spatial engrams and that they remain as sensitive as their pseudo-wild-type (p-WT) littermates to etomidate-induced suppression of place cells and spatial engrams. By contrast, mice with selective knockout in interneurons (α5-i-KO) no longer exhibit etomidate-induced suppression of place cells. In addition, the strength of spatial engrams is lower in α5-i-KO mice than p-WT littermates under control conditions. Consistent with the established role of the hippocampus in contextual fear conditioning, α5-i-KO mice resisted etomidate’s suppression of freezing to context, but so too did α5-pyr-KO mice, supporting a role for extra-hippocampal regions in the development of contextual fear memory. Overall, our results indicate that interneuronal α5-GABAARs serve a physiological role in promoting spatial learning and that they mediate suppression of hippocampus-dependent contextual memory by etomidate.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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