Moderate UVB exposure ameliorate chronic stress-induced anxiety and social impairment by activating mPFC to basal lateral amygdala pathway

IF 3.7 3区 医学 Q2 NEUROSCIENCES Brain Research Bulletin Pub Date : 2025-02-13 DOI:10.1016/j.brainresbull.2025.111260
Dake Song , Jingyu Qi , Yingying Zhang , Ruixia Liu , Min Wang , Xinshang Wang , Yumei Wu , Xubo Li , Kun Zhang , Shuibing Liu
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Abstract

Ultraviolet radiation B (UVB), the most biologically active ultraviolet ray in sunlight, exert broad effects on physiological and behavioral functions, including circadian rhythm, mood, and cognition. However, its underlying mechanisms are still unknown. In this study, in order to verify effects of UVB on anxiety and social behaviors, C57BL/6 mice receiving 2 h UVB exposure after chronic restraint stress were used. UVB exposure improved anxiety-like behaviors and social activities in normal and restraint stressed mice. Meanwhile, UVB exposure increased the neural excitability in mPFC according to cFos staining and electrophysiology results. And benefits of UVB exposure could be blocked by chemogenetical inhibition of mPFC or inhibiting mPFC to basal lateral amygdala (BLA) pathway. In conclusion, we identify UVB exposure ameliorate chronic stress-induced anxiety and social impairment by activating mPFC to BLA pathway. The series of research may lead to the development of UVB as a novel therapeutic approach for treating anxiety and social avoidance in the future.
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适度紫外线照射通过激活前脑皮质-基底外侧杏仁核通路,改善慢性应激诱发的焦虑和社交障碍
紫外线B (UVB)是阳光中最具生物活性的紫外线,对生理和行为功能具有广泛的影响,包括昼夜节律、情绪和认知。然而,其潜在机制尚不清楚。在本研究中,为了验证UVB对焦虑和社交行为的影响,我们使用慢性约束应激后暴露于2 h UVB的C57BL/6小鼠。UVB暴露改善了正常和受限应激小鼠的焦虑样行为和社交活动。同时,cFos染色和电生理结果显示,UVB暴露增加了mPFC的神经兴奋性。UVB暴露的益处可能通过抑制mPFC或抑制mPFC到基底外侧杏仁核(BLA)途径而被阻断。综上所述,我们发现UVB暴露通过激活mPFC - BLA通路改善慢性应激性焦虑和社交障碍。这一系列的研究可能会导致中波辐射在未来成为治疗焦虑和社交回避的一种新的治疗方法。
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来源期刊
Brain Research Bulletin
Brain Research Bulletin 医学-神经科学
CiteScore
6.90
自引率
2.60%
发文量
253
审稿时长
67 days
期刊介绍: The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.
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