Wang Ya-Tao, Li Yong, Li Meng-Yun, Zhang Yue-Ming, Wang Yue, Xu Qi-Qi, Liu Rong-Yu, Qin Xin-Ya, Shan Qing-Hong, Wang Yu, Zhou Jiang-Ning, Chen Peng
Institute of Brain Science, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Anhui Geriatrics Institute, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Neuropsychopharmacology. 2025 Jun 10. doi: 10.1038/s41386-025-02148-6.
Variations in individual coping styles have been linked to either resilience or vulnerability towards stress, thereby influencing the probability of developing stress-related disorders. The involvement of corticotropin-releasing factor (CRF) neurons within the medial prefrontal cortex (mPFC) plays a crucial role in modulating behavioral responses to stressful situations. In this study utilizing a mouse model of social defeat stress (SDS), we demonstrate how coordinated activation and localized release of CRF within the mPFC contribute to promoting adaptive responses under stressful conditions leading to enhanced resilience against subsequent challenges. Specifically, during SDS exposure, heightened activity levels were observed among mPFC CRF neurons coincide with increased local release triggered by active exploration and defensive behaviors, while decreased responses were detected upon exposure to aggression. Interestingly, the CRF neural activity and local release responding to coping behaviors throughout chronic social defeat stress (CSDS) differed between susceptible and resilient mice. Furthermore, activation of CRF receptor 1 (CRFR1) signaling in the mPFC enhanced active coping behaviors and conferred resilience to CSDS, while inhibition of CRF system promoted passive coping behaviors and induced susceptibility to sub-threshold SDS. Additionally, inhibition of CRFR1 in the mPFC nullified the pro-resilience effect elicited by activation of CRF neurons during CSDS. The collective findings provide evidence supporting the crucial role of local endogenous CRF derived from mPFC CRF neurons in maintaining resilience through active coping styles when confronted with social stress. Moreover, these results suggest that targeting the mPFC CRF system could hold promise as a therapeutic approach for managing stress-related disorders.
个体应对方式的差异与对压力的恢复力或易感性相关联,从而影响患压力相关疾病的可能性。内侧前额叶皮质(mPFC)内促肾上腺皮质激素释放因子(CRF)神经元的参与在调节对压力情境的行为反应中起着关键作用。在这项利用社会挫败应激(SDS)小鼠模型的研究中,我们证明了mPFC内CRF的协同激活和局部释放如何有助于在压力条件下促进适应性反应,从而增强对后续挑战的恢复力。具体而言,在SDS暴露期间,观察到mPFC CRF神经元的活动水平升高,这与主动探索和防御行为触发的局部释放增加相吻合,而在暴露于攻击时检测到反应减少。有趣的是,在慢性社会挫败应激(CSDS)期间,易感性小鼠和恢复力小鼠对应对行为的CRF神经活动和局部释放反应有所不同。此外,mPFC中CRF受体1(CRFR1)信号的激活增强了主动应对行为,并赋予了对CSDS的恢复力,而CRF系统的抑制则促进了被动应对行为,并诱导了对阈下SDS的易感性。此外,mPFC中CRFR1的抑制消除了CSDS期间CRF神经元激活所引发的促恢复力效应。这些共同的发现提供了证据,支持源自mPFC CRF神经元的局部内源性CRF在面对社会压力时通过主动应对方式维持恢复力方面的关键作用。此外,这些结果表明,针对mPFC CRF系统可能有望成为治疗压力相关疾病的一种方法。