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Herb Pair Danggui-Baishao: Pharmacological Mechanisms Underlying Primary Dysmenorrhea by Network Pharmacology Approach

机译:草药对当归-白药:通过网络药理学方法进行原发性痛经的药理机制

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Epidemiological studies have shown that primary dysmenorrhea is the most common disease in gynecology, and its incidence rate is between 20% and 90%, which is a common cause of affecting women's normal work and quality of life. Its high incidence rate, wide spread and economic losses and social harm have caused widespread concern worldwide. The present work adopted a network pharmacology-based approach to provide new insights into the active compounds and therapeutic targets of Danggui-Baishao herb pair for the treatment of primary dysmenorrhea. Fifteen active compounds of the herb pair possessing favorable pharmacokinetic profiles and biological activities were selected, interacting 17 dysmenorrhea-related targets to provide potential synergistic therapeutic actions. Systematic analysis of the constructed networks revealed that these targets such as ABCB1, ESR1, PGR, AKR1C3, PTGS2, CYP2C8, PTGS1 were mainly involved in Steroid hormone biosynthesis, Arachidonic acid metabolism, serotonergic synapse and Ovarian steroidogenesis through steroid metabolic process, steroid hormone mediated signaling pathway, cyclooxygenase pathway, response to estradiol and response to oxidative stress.
机译:流行病学研究表明,原发性痛经是妇科中最常见的疾病,其发病率在20%至90%之间,是影响​​妇女正常工作和生活质量的常见原因。它的高发病率,广泛传播以及经济损失和社会危害已引起全世界的广泛关注。目前的工作采用了基于网络药理学的方法,为当归-白草草药对治疗原发性痛经的活性化合物和治疗靶点提供了新的见解。选择了具有良好药代动力学特性和生物活性的草药对中的15种活性化合物,它们与17个痛经相关靶标相互作用,以提供潜在的协同治疗作用。对构建网络的系统分析表明,这些目标(例如ABCB1,ESR1,PGR,AKR1C3,PTGS2,CYP2C8,PTGS1)主要参与类固醇激素的生物合成,花生四烯酸代谢,血清素能突触和通过类固醇代谢过程的卵巢激素类固醇生成,类固醇激素介导信号途径,环氧合酶途径,对雌二醇的反应和对氧化应激的反应。

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