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整合网络药理学与实验模型以探究黄连解毒汤对脑缺血诱导的炎症损伤的作用机制

Integrating Network Pharmacology and Experimental Models to Investigate the Mechanism of Huanglian Jiedu Decoction on Inflammatory Injury Induced by Cerebral Ischemia.

作者信息

Li HuiMin, Lv Teng, Wang Bin, Li Min, Liu JiPing, Wang Chuan, Tang ZhiShu

机构信息

Shaanxi University of Chinese Medicine, Xianyang 712046, China.

出版信息

Evid Based Complement Alternat Med. 2021 Jan 13;2021:2135394. doi: 10.1155/2021/2135394. eCollection 2021.

DOI:10.1155/2021/2135394
PMID:33519941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7817265/
Abstract

Unlike single-target Western medicines, traditional Chinese medicines (TCMs) exhibit diverse curative effects against multiple diseases through their "multicomponent" and "multitarget" manifestations. However, the material basis of the major therapeutic diseases and TCM underlying molecular mechanisms remain to be challenged. In the current study, we applied, for the first time, an integrated strategy that combines network pharmacology and experimental evaluation and explored and demonstrated the underlying possible mechanisms of a classic TCM formula, Huanglian Jiedu Decoction (HLJD), in the treatment of cerebral ischemia. First, the herb compound, protein compound, and GO-BP and KEGG pathways were constructed to predict the material basis of HLJD in the treatment of cerebral ischemia and explore the underlying molecular mechanisms. Network pharmacology analysis showed that HLJD treats cerebral ischemia mainly through its anti-inflammatory effect. We used molecular docking to verify that HLJD components have good binding activities to the arachidonic acid pathway enzymes, cyclooxylipase-2 (COX-2) and 5-lipoxygenase (5-LOX). Next, based on the prediction by the network pharmacology analysis, the rat model of middle cerebral artery occlusion (MCAO) was established to verify the efficacy of HLJD. The results showed that HLJD reduces the degree of brain injury in MCAO rats, probably by inhibiting the expression of the 5-LOX pathway and inflammatory response. In conclusion, our study demonstrates the effectiveness of integrating network pharmacology with an experimental study for material basis of the major therapeutic diseases and the underlying molecular mechanisms of TCM.

摘要

与单一靶点的西药不同,中药通过其“多成分”和“多靶点”表现出对多种疾病的多样疗效。然而,主要治疗疾病的物质基础和中药潜在的分子机制仍有待挑战。在本研究中,我们首次应用了一种结合网络药理学和实验评估的综合策略,探索并证明了经典中药方剂黄连解毒汤(HLJD)治疗脑缺血的潜在可能机制。首先,构建了草药化合物、蛋白质化合物以及基因本体生物学过程(GO-BP)和京都基因与基因组百科全书(KEGG)通路,以预测HLJD治疗脑缺血的物质基础并探索潜在的分子机制。网络药理学分析表明,HLJD主要通过其抗炎作用治疗脑缺血。我们使用分子对接来验证HLJD成分对花生四烯酸途径酶环氧化酶-2(COX-2)和5-脂氧合酶(5-LOX)具有良好的结合活性。接下来,基于网络药理学分析的预测,建立了大脑中动脉闭塞(MCAO)大鼠模型以验证HLJD的疗效。结果表明,HLJD可能通过抑制5-LOX途径的表达和炎症反应来减轻MCAO大鼠的脑损伤程度。总之,我们的研究证明了将网络药理学与实验研究相结合对于阐明中药主要治疗疾病的物质基础和潜在分子机制的有效性。

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