首页> 外文期刊>Frontiers in Neuropharmacology >Danzhi Xiaoyao Powder Promotes Neuronal Regeneration by Downregulating Notch Signaling Pathway in the Treatment of Generalized Anxiety Disorder
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Danzhi Xiaoyao Powder Promotes Neuronal Regeneration by Downregulating Notch Signaling Pathway in the Treatment of Generalized Anxiety Disorder

机译:Danzhi Xiaoyao粉促进神经元再生通过下调Notch信号通路在治疗广泛性焦虑症

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Generalized anxiety disorder (GAD) is one of the most common types of anxiety disorders with unclear pathogenesis. Our team’s previous research found that extensive neuronal apoptosis and neuronal regeneration disorders occur in the hippocampus of GAD rats. Danzhi Xiaoyao (DZXYS) Powder can improve the anxiety behavior of rats, but its molecular mechanism is not well understood. This paper discusses whether the pathogenesis of GAD is related to the abnormal expression of Notch signal pathway, and whether the anti-anxiety effect of DZXYS promotes nerve regeneration in the hippocampus by regulating the Notch signaling pathway. Methods: The animal model of GAD was developed by the chronic restraint stress and uncertain empty bottle stimulation method. After the model was successfully established, the rats in the model preparation group were divided into the buspirone, DZXYS, DZXYS + DAPT, and model groups, and were administered the corresponding drug intervention. The changes in body weight and food intake of rats were continuously monitored throughout the process. The changes in anxiety behavior of rats were measured by open field experiment and elevated plus-maze test, and morphological changes and regeneration of neurons in the rat hippocampus were observed by HE staining and double immunofluorescence staining. Changes in the expression of key targets of the Notch signaling pathway in the hippocampus were monitored by real-time fluorescence quantitative PCR and western blotting. Results: In this study, we verified that the GAD model was stable and reliable, and found that the key targets of the Notch signaling pathway (Notch1, Hes1, Hes5, etc.) in the hippocampus of GAD rats were significantly upregulated, leading to the increased proliferation of neural stem cells in the hippocampus and increased differentiation into astrocytes, resulting in neuronal regeneration. DZXYS intervention in GAD rats can improve appetite, promote weight growth, and significantly reverse the anxiety behavior of GAD rats, which can inhibit the upregulation of key targets of the Notch signaling pathway, promote the differentiation of neural stem cells in the hippocampus into neurons, and inhibit their differentiation into astrocytes, thus alleviating anxiety behavior. Conclusion: The occurrence of GAD is closely related to the upregulation of the Notch signaling pathway, which hinders the regeneration of normal neurons in the hippocampus, while DZXYS can downregulate the Notch signaling pathway and promote neuronal regeneration in the hippocampus, thereby relieving anxiety behavior.
机译:广义焦虑症(GAD)是具有持不清理病发生的最常见类型的焦虑症之一。我们的团队以前的研究发现,在GAD大鼠的海马中发生了广泛的神经元细胞凋亡和神经元再生障碍。丹智小涛(DZXYS)粉末可以改善大鼠的焦虑行为,但其分子机制还不太了解。本文讨论了GAD的发病机制是否与陷波信号途径的异常表达有关,以及DZXYS的抗焦虑作用是否通过调节凹口信号通路来促进海马中的神经再生。方法:通过慢性约束应力和不确定空瓶刺激方法开发了GAD的动物模型。成功建立了模型后,模型制备组中的大鼠分为母线,DZXYS,DZXYS + DAPT和模型组,并进行了相应的药物干预。在整个过程中连续监测大鼠体重和食物摄入量的变化。通过开场实验测量大鼠焦虑行为的变化,并通过升高的正迷宫试验测量,并且通过染色和双免疫荧光染色观察大鼠海马神经元的形态变化和再生。通过实时荧光定量PCR和Western印迹监测海马中陷波信号通路的关键目标表达的变化。结果:在这项研究中,我们验证了GAD模型是稳定可靠的,发现在GAD大鼠的海马中陷波信号通路(Notch1,Hes1,Hes5等)的关键目标显着上调,导致在海马中的神经干细胞增殖增加,并增加分化为星形胶质细胞,导致神经元再生。 GAD大鼠的DZXYS干预可以改善食欲,促进体重增加,并显着逆转GAD大鼠的焦虑行为,这可以抑制陷波信号通路的关键目标的上调,促进海马神经干细胞的分化为神经元,并抑制他们分化成星形胶质细胞,从而减轻了焦虑行为。结论:GAD的发生与NOVCH信号通路的上调密切相关,阻碍了海马中正常神经元的再生,而DZXYS可以下调陷波信号通路并促进海马中的神经元再生,从而缓解焦虑行为。

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