Ge Hailong, Si Lujia, Li Chen, Huang Junjie, Sun Limin, Wu Lan, Xie Yinping, Xiao Ling, Wang Gaohua
Department of Psychiatry, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Department of Psychiatry, Institute of Neuropsychiatry, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Int J Mol Sci. 2025 Jan 27;26(3):1113. doi: 10.3390/ijms26031113.
Resveratrol, a plant-derived polyphenol, exhibits significant antidepressant effects and notably enhances neuroplasticity in neurological diseases. However, whether the antidepressant function of resveratrol is related to neuroplasticity remains uncertain, and the underlying mechanisms is poorly understood. This study aims to investigate the role and mechanism of resveratrol in neuroplasticity in depression. Here, we adopted the chronic unpredictable mild stress (CUMS) model and resveratrol intervention by oral gavage. Thereafter, behavioral tests confirmed resveratrol's antidepressant effect, and Nissl staining, Golgi staining, and Western blotting (WB) were employed to assess the neuronal plasticity. Moreover, proteomic analysis and WB were used to screen and identify the key proteins. To investigate the downstream target of ELAV-like RNA-binding protein 4 (ELAVL4) (one of candidate genes), the RNA Interactome Database and the National Center for Biotechnology Information databases were utilized to predict the targets of ELAVL4. Finally, Quantitative PCR, WB, and Immunofluorescence were used to verify the prediction. Our results indicate that resveratrol alleviates CUMS-induced depressive-like behaviors accompanied by the restoration of impaired hippocampal neuroplasticity. Then, proteomic analysis shows that 351 differentially expressed proteins (DEPs) decrease after CUMS, while 24 DEPs increase remarkably with the resveratrol treatment. Among which, ELAVL4 is downregulated by CUMS, simultaneously increasing after resveratrol intervention, which acts as a protective protein in this process. Finally, brain-derived neurotrophic factor () mRNA is predicted to be the potential target of ELAVL4 and validated by molecular technologies. In conclusion, our findings demonstrate that resveratrol's antidepressant efficacy is closely associated with ELAVL4, an RNA-binding protein, a mediated neuroplasticity pathway, potentially intersecting with the mRNA. Overall, this research sheds light on the role of the ELAVL4- mRNA pathway through neuroplasticity in resveratrol's antidepressant action, which provides an mRNA regulation perspective for the development of novel antidepressants and understanding depression pathology.
白藜芦醇是一种植物源多酚,具有显著的抗抑郁作用,尤其能增强神经疾病中的神经可塑性。然而,白藜芦醇的抗抑郁功能是否与神经可塑性相关仍不确定,其潜在机制也知之甚少。本研究旨在探讨白藜芦醇在抑郁症神经可塑性中的作用及机制。在此,我们采用慢性不可预测温和应激(CUMS)模型,并通过灌胃给予白藜芦醇进行干预。此后,行为测试证实了白藜芦醇的抗抑郁作用,并采用尼氏染色、高尔基染色和蛋白质免疫印迹法(WB)评估神经元可塑性。此外,蛋白质组学分析和WB用于筛选和鉴定关键蛋白。为了研究ELAV样RNA结合蛋白4(ELAVL4)(候选基因之一)的下游靶点,利用RNA相互作用组数据库和美国国立生物技术信息中心数据库预测ELAVL4的靶点。最后,采用定量PCR、WB和免疫荧光法验证预测结果。我们的结果表明,白藜芦醇可减轻CUMS诱导的抑郁样行为,并伴有受损海马神经可塑性的恢复。然后,蛋白质组学分析表明,CUMS后有351种差异表达蛋白(DEP)减少,而白藜芦醇处理后有24种DEP显著增加。其中,ELAVL4在CUMS后下调,白藜芦醇干预后同时上调,在此过程中起保护蛋白的作用。最后,脑源性神经营养因子()mRNA被预测为ELAVL4的潜在靶点,并通过分子技术得到验证。总之,我们的研究结果表明,白藜芦醇的抗抑郁功效与RNA结合蛋白ELAVL4密切相关,ELAVL4介导神经可塑性途径,可能与mRNA相交。总体而言,本研究揭示了ELAVL4-mRNA途径通过神经可塑性在白藜芦醇抗抑郁作用中的作用,为新型抗抑郁药的开发和抑郁症病理学的理解提供了mRNA调控视角。