[Jiawei Xiaoyao Pills improves depression-like behavior in rats by regulating neurotransmitters, inhibiting inflammation and oxidation and modulating intestinal flora].

Ying Liu, Borui Li, Yongcai Li, Lubo Chang, Jiao Wang, Lin Yang, Yonggang Yan, Kai Qv, Jiping Liu, Gang Zhang, Xia Shen
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引用次数: 0

Abstract

Objectives: To explore the bioactive components in Jiawei Xiaoyao Pills (JWXYP) and their mechanisms for alleviating depression-like behaviors.

Methods: The active compounds, key targets, and pathways of JWXYP were identified using TCMSP and TCMIP databases. Thirty-six SD rats were randomized equally into 6 groups including a control group and 5 chronic unpredictable mild stress (CUMS)-induced depression groups. After modeling, the 5 model groups were treated with daily gavage of normal saline, 1.8 mg/kg fluoxetine hydrochloride (positive control drug), or JWXYP at 1.44, 2.88, and 4.32 g/kg. The depression-like behaviors of the rats were evaluated using behavioral tests, and pathological changes in the liver and hippocampus were examined with HE staining. The biochemical indicators in the serum and brain tissues were detected using ELISA. Serum metabolomics analysis was performed to identify the differential metabolites using OPLS-DA, and gut microbiota changes were analyzed using 16S rDNA sequencing.

Results: Network pharmacology revealed that menthone and paeonol in JWXYP were capable of penetrating the blood-brain barrier to regulate inflammatory pathways and protect the nervous system. In the rat models subjected to CUMS, treatment with JWXYP significantly improved body weight loss, sucrose preference and open field activities, reduced liver inflammation, alleviated structural changes in the hippocampal neurons, decreased serum levels of TNF‑α, IL-1β, IL-6 and LBP, and increased 5-HT and VIP concentrations in the serum and brain tissue, and these effects were the most pronounced in the high-dose group. Metabolomics analysis showed changes in such metabolites as indole-3-acetamide and acetyl-L-carnitine in JWXYP-treated rats, involving the pathways for bile acid biosynthesis and amino acid metabolism. 16S rDNA analysis demonstrated increased gut microbiota diversity and increased abundance of Lactobacillus species in JWXYP-treated rats.

Conclusions: JWXYP alleviates depression-like symptoms in rats by regulating the neurotransmitters, inhibiting inflammation and oxidation, and modulating gut microbiota.

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[加味逍遥丸通过调节神经递质、抑制炎症和氧化、调节肠道菌群改善大鼠抑郁样行为]。
目的:探讨加味逍遥丸的生物活性成分及其缓解抑郁样行为的机制。方法:利用TCMSP和TCMIP数据库对JWXYP的活性成分、关键靶点和通路进行鉴定。将36只SD大鼠随机分为6组,包括1个对照组和5个慢性不可预知轻度应激(CUMS)诱导的抑郁组。造模后,5个模型组分别每日灌胃生理盐水、阳性对照药物盐酸氟西汀1.8 mg/kg或JWXYP 1.44、2.88、4.32 g/kg。采用行为学测试评价大鼠抑郁样行为,HE染色观察大鼠肝脏和海马的病理变化。采用ELISA法检测血清和脑组织生化指标。采用OPLS-DA进行血清代谢组学分析,鉴定差异代谢物;采用16S rDNA测序分析肠道菌群变化。结果:网络药理学结果显示,江蓠中薄荷酮和丹皮酚具有穿透血脑屏障,调节炎症通路,保护神经系统的作用。在CUMS大鼠模型中,JWXYP显著改善了体重减轻、蔗糖偏好和开放野活动,减轻了肝脏炎症,减轻了海马神经元的结构变化,降低了血清中TNF - α、IL-1β、IL-6和LBP的水平,增加了血清和脑组织中5-HT和VIP的浓度,且这些作用在高剂量组最为明显。代谢组学分析显示,jwxyp治疗大鼠代谢产物吲哚-3-乙酰胺和乙酰-左旋肉碱发生变化,涉及胆汁酸生物合成途径和氨基酸代谢途径。16S rDNA分析显示,jwxyp治疗的大鼠肠道微生物群多样性和乳酸杆菌种类丰度增加。结论:JWXYP通过调节神经递质,抑制炎症和氧化,调节肠道菌群,减轻大鼠抑郁样症状。
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来源期刊
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
208
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