4.7 Article

Comparative Transcriptional Analyses in the Nucleus Accumbens Identifies RGS2 as a Key Mediator of Depression-Related Behavior

Journal

BIOLOGICAL PSYCHIATRY
Volume 92, Issue 12, Pages 942-951

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2022.06.030

Keywords

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Funding

  1. National Institutes of Health [K99/R00 MH115096, R01MH051399, R01NS086444, R01NS086444S1, R01MH121829S1, R01MH121829, R01MH103322]

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This study used the California mouse social defeat model to identify stress-sensitive molecular targets relevant to women. The researchers found that Rgs2 was downregulated in female California mice and women with major depressive disorder under social defeat stress. Overexpression of Rgs2 in the NAc restored social approach and sucrose preference in stressed female California mice. Targeting Rgs2 may be a novel approach for treating treatment-resistant depression in women.
BACKGROUND: Major depressive disorder is one of the most commonly diagnosed mental illnesses worldwide, with a higher prevalence in women than in men. Although currently available pharmacological therapeutics help many individuals, they are not effective for most. Animal models have been important for the discovery of molecular alterations in stress and depression, but difficulties in adapting animal models of depression for females has impeded progress in developing novel therapeutic treatments that may be more efficacious for women. METHODS: Using the California mouse social defeat model, we took a multidisciplinary approach to identify stresssensitive molecular targets that have translational relevance for women. We determined the impact of stress on transcriptional profiles in male and female California mouse nucleus accumbens (NAc) and compared these results with data from postmortem samples of the NAc from men and women diagnosed with major depressive disorder. RESULTS: Our cross-species computational analyses identified Rgs2 (regulator of G protein signaling 2) as a transcript downregulated by social defeat stress in female California mice and in women with major depressive disorder. RGS2 plays a key role in signal regulation of neuropeptide and neurotransmitter receptors. Viral vectormediated overexpression of Rgs2 in the NAc restored social approach and sucrose preference in stressed female California mice. CONCLUSIONS: These studies show that Rgs2 acting in the NAc has functional properties that translate to changes in anxiety- and depression-related behavior. Future studies should investigate whether targeting Rgs2 represents a novel target for treatment-resistant depression in women.

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