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基于网络药理学分析探讨中药方剂逍遥散通过RIPK1-RIPK3-MLKL介导的坏死性凋亡对慢性应激诱导的抑郁小鼠模型的抗抑郁作用机制

Antidepressant Mechanism of Traditional Chinese Medicine Formula Xiaoyaosan in CUMS-Induced Depressed Mouse Model via RIPK1-RIPK3-MLKL Mediated Necroptosis Based on Network Pharmacology Analysis.

作者信息

Yan Zhi-Yi, Jiao Hai-Yan, Chen Jian-Bei, Zhang Kai-Wen, Wang Xi-Hong, Jiang You-Ming, Liu Yue-Yun, Xue Zhe, Ma Qing-Yu, Li Xiao-Juan, Chen Jia-Xu

机构信息

School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

Dongfang Hospital Affiliated to Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Pharmacol. 2021 Nov 19;12:773562. doi: 10.3389/fphar.2021.773562. eCollection 2021.

Abstract

Depression is a stress-related disorder that seriously threatens people's physical and mental health. Xiaoyaosan is a classical traditional Chinese medicine formula, which has been used to treat mental depression since ancient times. More and more notice has been given to the relationship between the occurrence of necroptosis and the pathogenesis of mental disorders. The purpose of present study is to explore the potential mechanism of Xiaoyaosan for the treatment of depression using network pharmacology and experimental research, and identify the potential targets of necroptosis underlying the antidepressant mechanism of Xiaoyaosan. The mice model of depression was induced by chronic unpredictable mild stress (CUMS) for 6 weeks. Adult C57BL/6 mice were randomly divided into five groups, including control group, chronic unpredictable mild stress group, Xiaoyaosan treatment group, necrostatin-1 (Nec-1) group and solvent group. Drug intervention performed from 4 to 6 week of modeling. The mice in Xiaoyaosan treatment group received Xiaoyaosan by intragastric administration (0.254 g/kg/d), and mice in CUMS group received 0.5 ml physiological saline. Meanwhile, the mice in Nec-1 group were injected intraperitoneally (i.p.) with Nec-1 (10 mg/kg/d), and the equivalent volume of DMSO/PBS (8.3%) was injected into solvent group mice. The behavior tests such as sucrose preference test, forced swimming test and novelty-suppressed feeding test were measured to evaluate depressive-like behaviors of model mice. Then, the active ingredients in Xiaoyaosan and the related targets of depression and necroptosis were compiled through appropriate databases, while the "botanical drugs-active ingredients-target genes" network was constructed by network pharmacology analysis. The expressions of RIPK1, RIPK3, MLKL, -MLKL were detected as critical target genes of necroptosis and the potential therapeutic target compounds of Xiaoyaosan. Furthermore, the levels of neuroinflammation and microglial activation of hippocampus were measured by detecting the expressions of IL-1β, Lipocalin-2 and IBA1, and the hematoxylin and eosin (H&E) stained was used to observe the morphology in hippocampus sections. After 6-weeks of modeling, the behavioral data showed that mice in CUMS group and solvent group had obvious depressive-like behaviors, and the medication of Xiaoyaosan or Nec-1 could improve these behavioral changes. A total of 96 active ingredients in Xiaoyaosan which could regulate the 23 key target genes were selected from databases. Xiaoyaosan could alleviate the core target genes in necroptosis and improve the hippocampal function and neuroinflammation in depressed mice. The activation of necroptosis existed in the hippocampus of CUMS-induced mice, which was closely related to the pathogenesis of depression. The antidepressant mechanism of Xiaoyaosan included the regulation of multiple targets in necroptosis. It also suggested that necroptosis could be a new potential target for the treatment of depression.

摘要

抑郁症是一种与应激相关的疾病,严重威胁人们的身心健康。逍遥散是一种经典的中药方剂,自古以来就被用于治疗精神抑郁。越来越多的人开始关注坏死性凋亡的发生与精神障碍发病机制之间的关系。本研究旨在通过网络药理学和实验研究探索逍遥散治疗抑郁症的潜在机制,并确定逍遥散抗抑郁机制中潜在的坏死性凋亡靶点。采用慢性不可预测温和应激(CUMS)诱导小鼠抑郁模型6周。将成年C57BL/6小鼠随机分为五组,包括对照组、慢性不可预测温和应激组、逍遥散治疗组、坏死素-1(Nec-1)组和溶剂组。在造模的第4至6周进行药物干预。逍遥散治疗组小鼠通过灌胃给予逍遥散(0.254 g/kg/d),CUMS组小鼠给予0.5 ml生理盐水。同时,Nec-1组小鼠腹腔注射Nec-1(10 mg/kg/d),溶剂组小鼠注射等量体积的二甲基亚砜/磷酸盐缓冲液(8.3%)。通过蔗糖偏好试验、强迫游泳试验和新奇抑制摄食试验等行为测试来评估模型小鼠的抑郁样行为。然后,通过合适的数据库收集逍遥散中的活性成分以及抑郁症和坏死性凋亡的相关靶点,通过网络药理学分析构建“植物药-活性成分-靶基因”网络。检测RIPK1、RIPK3、MLKL、-MLKL的表达作为坏死性凋亡的关键靶基因和逍遥散潜在的治疗靶点化合物。此外,通过检测IL-1β、脂质运载蛋白-2和IBA1的表达来测量海马体的神经炎症水平和小胶质细胞激活情况,并采用苏木精-伊红(H&E)染色观察海马体切片的形态。造模6周后,行为数据显示,CUMS组和溶剂组小鼠有明显的抑郁样行为,逍遥散或Nec-1用药可改善这些行为变化。从数据库中筛选出逍遥散中96种可调节23个关键靶基因的活性成分。逍遥散可减轻坏死性凋亡中的核心靶基因,改善抑郁小鼠的海马功能和神经炎症。CUMS诱导的小鼠海马体中存在坏死性凋亡的激活,这与抑郁症的发病机制密切相关。逍遥散的抗抑郁机制包括对坏死性凋亡中多个靶点的调节。这也表明坏死性凋亡可能是治疗抑郁症的一个新的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e32b/8641697/d679cf4d6564/fphar-12-773562-g001.jpg

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