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A Biomedical Investigation of the Hepatoprotective Effect of Radix salviae miltiorrhizae and Network Pharmacology-Based Prediction of the Active Compounds and Molecular Targets

机译:丹参肝保肝作用的生物医学研究以及基于网络药理学的活性化合物和分子靶标预测

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Radix salviae miltiorrhizae (Danshen in Chinese), a classic traditional Chinese medicine (TCM) herb, has been used for centuries to treat liver diseases. In this study, the preventive and curative potential of Danshen aqueous extract on acute/chronic alcoholic liver disease (ALD) and non-alcoholic fatty liver disease (NAFLD) was studied. The in vivo results indicated that Danshen could alleviate hepatic inflammation, fatty degeneration, and haptic fibrogenesis in ALD and NAFLD models. In the aspect of mechanism of action, the significant reduction in MDA levels in both ALD and NAFLD models implies the decreased levels of oxidative stress by Danshen. However, Danshen treatment could not activate the internal enzymatic antioxidant system in ALD and NAFLD models. To further explore the hepatoprotective mechanism of Danshen, an in silico-based network pharmacology approach was employed in the present study. The pharmacological network analysis result revealed that six potential active ingredients such as tanshinone iia, salvianolic acid b, and Danshensu may contribute to the hepatoprotective effects of Danshen on ALD and NAFLD. The action mechanism may relate with regulating the intracellular molecular targets such as PPARα, CYP1A2, and MMP2 for regulation of lipid metabolism, antioxidant and anti-fibrogenesis by these potential active ingredients. Our studies suggest that the combination of network pharmacology strategy with in vivo experimental study may provide a forceful tool for exploring the mechanism of action of traditional Chinese medicine (TCM) herb and developing novel bioactive ingredients.
机译:丹参(丹参)是一种经典的传统中药(TCM),已经使用了多个世纪来治疗肝脏疾病。在这项研究中,丹参水提物对急性/慢性酒精性肝病(ALD)和非酒精性脂肪肝(NAFLD)的预防和治疗潜力进行了研究。体内结果表明,丹参可以减轻ALD和NAFLD模型中的肝脏炎症,脂肪变性和触觉纤维形成。在作用机理方面,ALD和NAFLD模型中MDA水平的显着降低表明丹参降低了氧化应激水平。但是,丹参治疗不能激活ALD和NAFLD模型中的内部酶抗氧化剂系统。为了进一步探讨丹参的保肝机制,本研究采用了基于计算机的网络药理学方法。药理网络分析结果显示,丹参酮iia,丹酚酸b和丹参素等6种潜在活性成分可能有助于丹参对ALD和NAFLD的保肝作用。作用机制可能与调节细胞内分子靶标(例如PPARα,CYP1A2和MMP2)有关,以通过这些潜在的活性成分调节脂质代谢,抗氧化剂和抗纤维化。我们的研究表明,网络药理学策略与体内实验研究的结合可能为探索中药(TCM)的作用机理和开发新的生物活性成分提供有力的工具。

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