The NMDA receptor subunit GluN2D is a potential target for rapid antidepressant action

Ketamine is the first glutamatergic agent in clinical use for major depression, but its primary target remains unclear. Further research is needed to develop more specific interventions with fewer side effects. Ketamine is a noncompetitive antagonist of the glutamatergic N-methyl-D-aspartate (NMDA) receptor. Here, we show that ketamine preferentially targets GluN2D-containing NMDA receptors on interneurons, and that selective GluN2D antagonism is sufficient to produce rapid antidepressant-like effects. We use ketamine, the selective GluN2C/D inhibitor NAB-14, Grin2d-siRNA and chemogenetic approaches in hippocampal slices and in vivo mice. We find that GluN2D antagonism inhibits NMDAR currents in interneurons but not pyramidal cells, and that GluN2D-mediated recruitment of GABAergic interneurons controls inhibitory circuits regulating hippocampal activity and plasticity. In a mouse model of depression, GluN2D inhibition recovers excitation-inhibition balance, restores plasticity, and mimics antidepressant-like actions of ketamine with fewer side effects. These findings identify GluN2D as a highly specific target for novel antidepressant therapy.

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Publication Details

Journal
Nature Communications
Published
2025-11-26
DOI
https://doi.org/10.1038/s41467-025-66774-w
Citations
2
Primary Topic
Treatment of Major Depression
Type
article
Field-Weighted Citation Impact
2.79
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article

The NMDA receptor subunit GluN2D is a potential target for rapid antidepressant action

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2 citations
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Treatment of Major Depression
2.79
article

The NMDA receptor subunit GluN2D is a potential target for rapid antidepressant action

Katharina Domschke, Magdalena N. Wojtas, Stefan Günther, Justin Wendel, Tsvetan Serchov, Claus Normann, Elisabeth Wendler, Catherine du Vinage, Shira Knafo, Nicole Gensch, Guillermo A. Suárez, Stefan Vestring, Aurélien F. A. Moumbock, Josef Bischofberger, James Warneke, Franziska Heynicke, Alice Theiß, Lovis M. Würz, Maxime Veleanu, Sabine Voita, Anna Li, David H. Sarrazin, Lotta M. Borger, Jakob Brandl, Clotilde Vivet, Dorothea Jocher, Pauline Loewe, Simon Barmann, Lea Smoltczyk, Granita Lokaj, Elisa Grießbach, Julia Lais, Martin Bronnec, Fatih Erdogdu, Judith Bernhardt, David Weigel, Prejwal Prabhakaran, S. Zimmermann, Johanna Moos, Fabian Hummel, Marina Conde Perez, Julia Stocker, Louise E. Schuberth, Jean-Paul Grohe
article en
2 citations

Abstract

Ketamine is the first glutamatergic agent in clinical use for major depression, but its primary target remains unclear. Further research is needed to develop more specific interventions with fewer side effects. Ketamine is a noncompetitive antagonist of the glutamatergic N-methyl-D-aspartate (NMDA) receptor. Here, we show that ketamine preferentially targets GluN2D-containing NMDA receptors on interneurons, and that selective GluN2D antagonism is sufficient to produce rapid antidepressant-like effects. We use ketamine, the selective GluN2C/D inhibitor NAB-14, Grin2d-siRNA and chemogenetic approaches in hippocampal slices and in vivo mice. We find that GluN2D antagonism inhibits NMDAR currents in interneurons but not pyramidal cells, and that GluN2D-mediated recruitment of GABAergic interneurons controls inhibitory circuits regulating hippocampal activity and plasticity. In a mouse model of depression, GluN2D inhibition recovers excitation-inhibition balance, restores plasticity, and mimics antidepressant-like actions of ketamine with fewer side effects. These findings identify GluN2D as a highly specific target for novel antidepressant therapy.

Nature CommunicationsVol. 16(1)
Ikerbasque (ES), Ben-Gurion University of the Negev (IL), Centre National de la Recherche Scientifique (FR), University of Freiburg (DE), University of the Basque Country (ES), University of Basel (CH), University Medical Center Freiburg (DE), Institut des Neurosciences Cellulaires et Intégratives (FR), German Centre for Cardiovascular Research (DE), Université de Strasbourg (FR)
Openalex Percentile: Top 8%
Treatment of Major Depression
2.79
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