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中药方剂9002A治疗阿尔茨海默病的药效学、网络药理学及药代动力学

Pharmacodynamics, Network Pharmacology, and Pharmacokinetics of Chinese Medicine Formula 9002A in the Treatment of Alzheimer's Disease.

作者信息

Tang Chunlan, Fang Zhiling, Chu Donghui, Zhang Lulu, Tang Yuqing, Zhou Jinyue, Fang Rui, Ying Jiaming, Wang Fang, Zhou Yuping, Xu Chunshuang, Wang Qinwen

机构信息

The Affiliated Hospital of Medical School, Ningbo University, Ningbo, China.

School of Medicine, Ningbo University, Ningbo, China.

出版信息

Front Pharmacol. 2022 Apr 8;13:849994. doi: 10.3389/fphar.2022.849994. eCollection 2022.

Abstract

Alzheimer's disease (AD) is a common and serious neurodegenerative disease in the elderly; however, the treatment of AD is still lacking of rational drugs. In this paper, the active constituents and targets of the self-developed Chinese medicine Formula 9002A in the treatment of AD were investigated from three aspects: pharmacodynamics based on cell and animal experiments, network pharmacology analysis, and pharmacokinetic analysis. A total of 124 compounds were screened in Formula 9002A, and four constituents including salidroside, gastrodin, niacinamide, and umbelliferone were screened as potential active components for the treatment of AD by network pharmacology. Among them, salidroside and gastrodin showed higher relevance with AD targets, such as ESR1 and AR. The pharmacokinetic study showed that they could be absorbed and identified in plasma; the half-life and mean residence times of salidroside and gastrodin in plasma were nearly increased 2-fold by the administration of Formula 9002A compared with those by the administration of a monomer, indicating the extended action time of active compounds . Formula 9002A exerted the efficacy in the treatment of AD mainly by regulating APP, GSK3β, ESR1, and AR targets based on the anti-β-amyloid protein deposition, anti-oxidation and anti-apoptosis pathways. Two genes enriched in Alzheimer's disease pathway, APP and GSK3β, were further validated. The experiments also demonstrated that Formula 9002A could downregulate APP and GSK3β protein expression in the model mice brain and improved their cognitive ability. In summary, Formula 9002A has the characteristics of multiple targets and multiple pathways in the treatment of AD, and salidroside and gastrodin might be the main active constituents, which could provide a foundation for further research and application.

摘要

阿尔茨海默病(AD)是老年人中常见且严重的神经退行性疾病;然而,AD的治疗仍缺乏合理有效的药物。本文从基于细胞和动物实验的药效学、网络药理学分析以及药代动力学分析三个方面,对自主研发的中药方剂9002A治疗AD的活性成分及靶点进行了研究。在方剂9002A中共筛选出124种化合物,通过网络药理学筛选出红景天苷、天麻素、烟酰胺和伞形花内酯4种成分作为治疗AD的潜在活性成分。其中,红景天苷和天麻素与AD靶点如ESR1和AR的相关性较高。药代动力学研究表明,它们能够在血浆中被吸收和鉴定;与单体给药相比,方剂9002A给药后红景天苷和天麻素在血浆中的半衰期和平均驻留时间几乎增加了2倍,表明活性化合物的作用时间延长。基于抗β-淀粉样蛋白沉积、抗氧化和抗凋亡途径,方剂9002A主要通过调节APP、GSK3β、ESR1和AR靶点发挥治疗AD的功效。对阿尔茨海默病通路中富集的两个基因APP和GSK3β进行了进一步验证。实验还表明,方剂9002A可下调模型小鼠脑内APP和GSK3β蛋白表达,并改善其认知能力。综上所述,方剂9002A在治疗AD方面具有多靶点、多途径的特点,红景天苷和天麻素可能是主要活性成分,可为进一步的研究和应用提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cc9/9026172/199df19ef744/fphar-13-849994-g001.jpg

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