QRFP and GPR103 in the paraventricular nucleus play a role in chronic stress-induced depressive-like symptomatology by enhancing the hypothalamic-pituitary-adrenal axis

Hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis during chronic stress is essential for depression neurobiology. As the latest member of the RFamide peptide family in mammals, pyroglutamylated RFamide peptide (QRFP) is closely implicated in neuroendocrine maintenance by activating G-pr...

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Veröffentlicht in:Neuropharmacology 2025-01, Vol.262, p.110198, Article 110198
Hauptverfasser: Chen, Yan-Mei, Huang, Jie, Fan, Hua, Li, Wei-Yu, Shi, Tian-Shun, Zhao, Jie, Wang, Cheng-Niu, Chen, Wei-Jia, Zhu, Bao-Lun, Qian, Jun-Jie, Guan, Wei, Jiang, Bo
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Sprache:eng
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Zusammenfassung:Hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis during chronic stress is essential for depression neurobiology. As the latest member of the RFamide peptide family in mammals, pyroglutamylated RFamide peptide (QRFP) is closely implicated in neuroendocrine maintenance by activating G-protein-coupled receptor 103 (GPR103). We hypothesized that QRFP and GPR103 might contribute to chronic stress-induced depression by promoting corticotropin-releasing hormone (CRH) release from neurons in the paraventricular nucleus (PVN), and various methods were employed in this study, with male C57BL/6J mice adopted as the experimental subjects. Chronic stress induced not only depression-like behaviors but also significant enhancement in QRFP and GPR103 in the PVN. Genetic overexpression of QRFP/GPR103 and stereotactic infusion of QRFP-26/QRFP-43 peptide in the PVN all mimicked chronic stress that induced various depression-like phenotypes in naïve mice, and this was mediated by promoting CRH biosynthesis and HPA activity. In contrast, genetic knockdown of QRFP/GPR103 in the PVN produced notable antidepressant-like effects in mice exposed to chronic stress. Furthermore, genetic knockout of QRFP also protected against chronic stress in mice. In addition, both the C-terminal biological region of QRFP and the downstream PKA/PKC-CREB signaling coupled to GPR103 stimulation underlie the role of QRFP and GPR103 in depression. Collectively, QRFP and GPR103 in PVN neurons could be viable targets for novel antidepressants. •Chronic stress evidently enhanced QRFP and GPR103 expression in the PVN.•Overexpression of QRFP/GPR103 in the PVN induced various depressive-like phenotypes in naïve mice.•Knockdown of QRFP/GPR103 in the PVN produced significant antidepressant-like effects in mice.•The downstream PKA/PKC-CREB-CRH pathway underlies the role of QRFP and GPR103 in depression.
ISSN:0028-3908
1873-7064
1873-7064
DOI:10.1016/j.neuropharm.2024.110198