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Analysis of Potential Mechanism of Herbal Formula Taohong Siwu Decoction against Vascular Dementia Based on Network Pharmacology and Molecular Docking

机译:基于网络药理学和分子对接的中药方桃红思雾汤治疗血管性痴呆的潜在机制分析

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Vascular dementia (VaD) is the second most prevalent dementia, which is attributable to neurovascular dysfunction. Currently, no approved pharmaceuticals are available. Taohong Siwu decoction (TSD) is a traditional Chinese medicine prescription with powerful antiapoptosis and anti-inflammatory properties. In this study, a network pharmacology approach together with molecular docking validation was used to explore the probable mechanism of action of TSD against VaD. A total of 44 active components, 202 potential targets of components, and 3,613 VaD-related targets including 161 intersecting were obtained. The potential chemical components including kaempferol, baicalein, beta-carotene, luteolin, quercetin, and beta-sitosterol involved in the inflammatory response, oxidative stress, and apoptosis might have potential therapeutic effects on the treatment of VaD. The potential core targets including AKT1, CASP3, IL1 β , JUN, and TP53 associated with cell apoptosis and inflammatory might account for the essential therapeutic effects of TSD in VaD. The results indicated that TSD protected against VaD through multicomponent and multitarget modes. Though the detailed mechanism of action of various active ingredients needs to be further illustrated, TSD still showed a promising therapeutic agent for VaD due to its biological activity.
机译:血管性痴呆 (VaD) 是第二常见的痴呆,可归因于神经血管功能障碍。目前,尚无获批的药物。桃红思悟汤(TSD)是一种传统中药处方,具有强大的抗细胞凋亡和抗炎特性。本研究采用网络药理学方法结合分子对接验证,探讨TSD对VaD的可能作用机制。共获得44个活性成分、202个成分潜在靶点和3,613个VaD相关靶点,包括161个相交靶点。山奈酚、黄芩素、β-胡萝卜素、木犀草素、槲皮素和β-谷甾醇等潜在化学成分参与炎症反应、氧化应激和凋亡可能对VaD的治疗具有潜在的治疗效果。与细胞凋亡和炎症相关的AKT1、CASP3、IL1 β、JUN和TP53等潜在核心靶点可能是TSD在VaD中的重要治疗作用的原因。结果表明,TSD通过多分量和多靶点模式对VaD有保护作用。尽管各种活性成分的详细作用机制还有待进一步说明,但由于其生物活性,TSD仍然显示出一种有前途的VaD治疗剂。

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