GluN2D expression is regulated by restraint stress and supports active stress coping bouts. (1st March 2023)

• Record Type: Journal Article
• Authors: Doyle, Marie A.; Brown, Jordan A.; Winder, Danny G.
• Is Part Of: Neuropharmacology. Volume 225(2023)
• Publication Date: 2023-03-01
• Subjects: BNST -- GluN2D -- Restraint stress -- Coping strategies; Neuropsychopharmacology -- Periodicals; Autonomic Agents -- Periodicals; Neuropsychopharmacologie -- Périodiques; Neuropsychopharmacology; Periodicals; Electronic journals; 615.78
• DOI: 10.1016/j.neuropharm.2022.109377
• Languages: English
• ISSNs: 0028-3908

Abstract

Abstract: Stress coping strategies represent critical responses to environmental challenges, and active coping has been linked to stress resilience in humans. Understanding the neuroadaptations that support these strategies may provide insights into adaptive and maladaptive stress responses. NMDA receptors (NMDARs) play key roles in neuroadaptation, and NMDARs have been specifically implicated in stress responsiveness. Constitutive knockout mice have been used to implicate the GluN2D NMDAR subunit in regulation of stress-sensitive and affective behavior, but the brain regions in which GluN2D expression changes drive these effects remain unknown. Here we report that following an acute restraint stressor, GluN2D subunit expression is specifically decreased in the bed nucleus of the stria terminalis (BNST), a key region involved in stress processing, in male but not female mice, with no differences found in the thalamus or ventral hippocampus in either sex. Rodents engage in active struggling events during restraint stress that may represent active coping strategies to stress. Thus, we assessed active coping bouts during acute and chronic restraint stress sessions in GluN2D knockout mice. During the first restraint session, GluN2D knockout mice exhibited a pronounced decrease in struggling bouts during restraint stress relative to wild-type littermates, consistent with a role of GluN2D in active coping responses to stress. Repeated, daily restraint sessions revealed a sex-specific role of GluN2D expression on certain aspects of active coping behaviors, with male GluN2D KO mice exhibiting a decrease in total coping bouts measured across five sessions. However, BNST-specific knockdown of GluN2D in male mice did not alter active coping bouts, suggesting either a multi-synaptic role of GluN2D and/or a developmental role of GluN2D in this behavior. Altogether, these data are consistent with a growing literature suggesting that exploration of GluN2D control of stress circuit actions may lead to a novel therapeutic target to consider for stress-related mood disorders. Highlights: Total GluN2D protein levels are decreased in the BNST of male, but not female, mice following an acute restraint stressor. Constitutive GluN2D knockout mice show a deficit in active coping bout behavior during a single restraint stressor. Male constitutive GluN2D knockout mice display fewer active coping bouts across repeated restraint stress sessions. Knockdown of BNST GluN2D in male mice does not recapitulate deficits in active coping bout behaviors observed during a single restraint session.