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Publication : Enhancing HIF-1α-P2X2 signaling in dorsal raphe serotonergic neurons promotes psychological resilience.

First Author  Zhang Y Year  2024
Journal  Redox Biol Volume  69
Pages  103005 PubMed ID  38150991
Mgi Jnum  J:349267 Mgi Id  MGI:7578353
Doi  10.1016/j.redox.2023.103005 Citation  Zhang Y, et al. (2024) Enhancing HIF-1alpha-P2X2 signaling in dorsal raphe serotonergic neurons promotes psychological resilience. Redox Biol 69:103005
abstractText  Major depressive disorder (MDD) is a devastating condition. Although progress has been made in the past seven decades, patients with MDD continue to receive an inadequate treatment, primarily due to the late onset of first-line antidepressant drugs and to their acute withdrawal symptoms. Resilience is the ability to rebound from adversity in a healthy manner and many people have psychological resilience. Revealing the mechanisms and identifying methods promoting resilience will hopefully lead to more effective prevention strategies and treatments for depression. In this study, we found that intermittent hypobaric hypoxia training (IHHT), a method for training pilots and mountaineers, enhanced psychological resilience in adult mice. IHHT produced a sustained antidepressant-like effect in mouse models of depression by inducing long-term (up to 3 months after this treatment) overexpression of hypoxia-inducible factor (HIF)-1alpha in the dorsal raphe nucleus (DRN) of adult mice. Moreover, DRN-infusion of cobalt chloride, which mimics hypoxia increasing HIF-1alpha expression, triggered a rapid and long-lasting antidepressant-like effect. Down-regulation of HIF-1alpha in the DRN serotonergic (DRN(5-HT)) neurons attenuated the effects of IHHT. HIF-1alpha translationally regulated the expression of P2X2, and conditionally knocking out P2rx2 (encodes P2X2 receptors) in DRN(5-HT) neurons, in turn, attenuated the sustained antidepressant-like effect of IHHT, but not its acute effect. In line with these results, a single sub-anesthetic dose of ketamine enhanced HIF-1alpha-P2X2 signaling, which is essential for its rapid and long-lasting antidepressant-like effect. Notably, we found that P2X2 protein levels were significantly lower in the DRN of patients with MDD than that of control subjects. Together, these findings elucidate the molecular mechanism underlying IHHT promoting psychological resilience and highlight enhancing HIF-1alpha-P2X2 signaling in DRN(5-HT) neurons as a potential avenue for screening novel therapeutic treatments for MDD.
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