Metformin attenuated depressive-like behaviors by suppressing TRPV1/NLRP3 mediated neuroinflammation in the hypothalamus of allergic rhinitis mice

IF 2.8 3区 医学 Q2 NEUROSCIENCES Neuroscience Pub Date : 2025-04-06 Epub Date: 2025-01-21 DOI:10.1016/j.neuroscience.2025.01.043
Yunfei Wang , Yulie Xie , Peiqiang Liu , Hao Lv , Mengting Guan , Jianchao Cong , Yan Wang , Yu Xu
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Abstract

In addition to nasal symptoms, allergic rhinitis (AR) has increasingly been reported to be associated with depression-like behaviors. Recent evidence suggests that neuroinflammation in the hypothalamus may cause these depressive symptoms in AR. However, the precise mechanisms and effective treatments remain to be elucidated. This study investigated the ameliorative effects of metformin on neuroinflammation in the hypothalamus, depressive-like behavior and the underlying molecular mechanisms of AR mice. Mice were administered ovalbumin (OVA) intranasally to induce allergic rhinitis and subsequently subjected to behavioral experiments to detect depressive-like behavior. The roles of the TRPV1/NLRP3 pathway in depression-like behaviors in AR were examined in vivo. Additionally, the mechanism of TRPV1/NLRP3-mediated neuroinflammation was investigated in vitro. Finally, metformin was utilized to explore its possible mechanisms and efficacy in treating depressive-like behavior in AR. AR mice exhibited significant depressive-like behavior, which was attenuated by metformin. The number of Iba-1+ microglia significantly increased in the hypothalamus of AR mice. The expression of NLRP3 was significantly upregulated in the hypothalamus, activating microglia. Metformin ameliorated the neuropsychiatric symptoms by reducing NLRP3 expression in the hypothalamus. Moreover, metformin inhibited LPS-induced upregulation of the TRPV1/NLRP3 signaling pathway in microglial cell line, an effect that can be reversed by the TRPV1-specific agonist capsaicin. Increased TRPV1 expression activates the NLRP3 inflammasome in hypothalamic microglia, promoting the pathological process of depressive-like behavior in AR mice. Metformin could effectively treat neuroinflammation by regulating microglia via TRPV1 downregulation, indicating its potential as a treatment for depressive-like behaviors in AR.

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二甲双胍通过抑制变应性鼻炎小鼠下丘脑TRPV1/NLRP3介导的神经炎症来减轻抑郁样行为。
背景:除了鼻腔症状外,越来越多的报道称过敏性鼻炎(AR)与抑郁样行为有关。最近的证据表明,下丘脑的神经炎症可能导致AR中的这些抑郁症状。然而,确切的机制和有效的治疗方法仍有待阐明。目的:探讨二甲双胍对AR小鼠下丘脑神经炎症、抑郁样行为的改善作用及其分子机制。方法:小鼠鼻内注射卵清蛋白(OVA)诱导变应性鼻炎,随后进行行为实验以检测抑郁样行为。在体内研究TRPV1/NLRP3通路在AR抑郁样行为中的作用。此外,我们还在体外研究了TRPV1/ nlrp3介导的神经炎症机制。结果:AR小鼠表现出明显的抑郁样行为,但二甲双胍能减轻抑郁样行为。AR小鼠下丘脑Iba-1+小胶质细胞数量显著增加。NLRP3在下丘脑的表达显著上调,激活小胶质细胞。二甲双胍通过降低下丘脑NLRP3的表达来改善神经精神症状。此外,二甲双胍抑制lps诱导的小胶质细胞系中TRPV1/NLRP3信号通路的上调,这一作用可以被TRPV1特异性激动剂辣椒素逆转。结论:TRPV1表达升高激活下丘脑小胶质细胞NLRP3炎性体,促进AR小鼠抑郁样行为的病理过程。二甲双胍可以通过下调TRPV1调控小胶质细胞,有效治疗神经炎症,提示其有可能治疗AR中的抑郁样行为。
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来源期刊
Neuroscience
Neuroscience 医学-神经科学
CiteScore
6.20
自引率
0.00%
发文量
394
审稿时长
52 days
期刊介绍: Neuroscience publishes papers describing the results of original research on any aspect of the scientific study of the nervous system. Any paper, however short, will be considered for publication provided that it reports significant, new and carefully confirmed findings with full experimental details.
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