Glutamatergic Supramammillary Nucleus Neurons Respond to Threatening Stressors and Promote Active Coping

Author:

Escobedo Abraham1,Holloway Salli-Ann1,Votoupal Megan2,Cone Aaron L1,Skelton Hannah E1,Legaria Alex A.34ORCID,Ndiokho Imeh5,Floyd Tasheia6,Kravitz Alexxai V.134ORCID,Bruchas Michael R.78910ORCID,Norris Aaron J.1ORCID

Affiliation:

1. Department of Anesthesiology, Washington University in St. Louis

2. Department of Medicine, Northwestern University Feinberg School of Medicine

3. Department of Neuroscience, Washington University in St. Louis

4. Department of Psychiatry, Washington University in St. Louis

5. Medical College of Wisconsin

6. Department of Obstetrics and Gynecology, Washington University in St. Louis

7. Center for Neurobiology of Addiction

8. Department of Anesthesiology and Pain Medicine University of Washington

9. Department of Pharmacology University of Washington

10. Department of Bioengineering University of Washington

Abstract

Threat-response neural circuits are conserved across species and play roles in normal behavior and psychiatric diseases. Maladaptive changes in these neural circuits contribute to stress, mood, and anxiety disorders. Active coping in response to stressors is a psychosocial factor associated with resilience against stress-induced mood and anxiety disorders. The neural circuitry underlying active coping is poorly understood, but the functioning of these circuits could be key for overcoming anxiety and related disorders. The supramammillary nucleus (SuM) has been suggested to be engaged by threat. SuM has many projections and contains a poorly understood diversity of populations. We identified a unique population of glutamatergic SuM neurons (SuM VGLUT2+ ::POA) based on projection to the preoptic area of the hypothalamus (POA) and found SuM VGLUT2+ ::POA neurons have extensive arborizations. SuM VGLUT2+ ::POA neurons project to brain areas that mediate various features of the stress and threat responses including the paraventricular nucleus thalamus (PVT), periaqueductal gray (PAG), and the habenula (Hb). Thus, SuM VGLUT2+ ::POA neurons are positioned as a hub, connecting to areas implicated in regulating stress responses. Here we report SuM VGLUT2+ ::POA neurons are recruited by diverse threatening stressors, and recruitment of SuM VGLUT2+ ::POA neurons correlated with active coping behaviors. We found that selective photoactivation of the SuM VGLUT2+ ::POA population drove aversion but not anxiety like behaviors. Activation of SuM VGLUT2+ ::POA neurons in the absence of acute stressors evoked active coping like behaviors and drove instrumental behavior (selective port activations) ( Figure 6 ). Also, activation of SuM VGLUT2+ ::POA neurons was sufficient to convert passive coping strategies to active behaviors during acute stress. In contrast, we found activation of GABAergic (VGAT+) SuM neurons (SuM VGAT+ ) neurons did not alter drive aversion or active coping, but termination of photostimulation was followed by increased mobility in the forced swim test. These findings establish a new node in stress response circuitry that has projections to many brain areas, evokes flexible active coping behaviors, and offers new opportunities for furthering our neurobiological understanding of stress.

Publisher

eLife Sciences Publications, Ltd

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