Integrating network pharmacology and experimental validation to explore the mitophagy-associated pharmacological mechanism of modified Shisiwei Jianzhong decoction against aplastic anemia

IF 1.8 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Yun Zhang, Jun Wang, Bo Wang, Yanting Gao, Shengyun Lin, Yuhong Zhou, Liqiang Wu
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引用次数: 0

Abstract

The aim of this work was to investigate the therapeutic effect of modified Shisiwei Jianzhong Decoction (SJD) on aplastic anemia (AA) and its potential pharmacological mechanism from the perspective of mitophagy. A comprehensive approach combining network pharmacology, mendelian randomization, molecular docking and animal experiments was applied to evaluate the properties of SJD against AA. By integrating multiple databases, it was determined that SJD exerted its therapeutic effect on AA by targeting three key targets [mammalian target of rapamycin (MTOR), poly(ADP-ribose) polymerase 1 (PARP1) and Sirtuin 1 (SIRT1)] through four core compounds (quercetin, resveratrol, genistein and curcumin). Mendelian randomization analysis identified MTOR as a risk factor for AA occurrence while PARP1 was a protective factor. Results of animal experiments showed that SJD improved peripheral blood counts and promoted the proliferation of hematopoietic stem cells. Mechanistically, SJD, especially at high dose, played a therapeutic role in AA by activating mitophagy-related proteins PTEN induced kinase 1 (PINK1)/Parkin and inhibiting the phosphatidylinositol 3-kinase (PI3K)/protein kinase (AKT)/MTOR pathway. This study revealed for the first time the core chemical composition of SJD and its pharmacological effects against AA, which can restore hematopoietic function by activating mitophagy. The results provide inspiration for the clinical application of traditional Chinese medicine in AA treatment.

整合网络药理学和实验验证,探索改良的四味建中煎剂抗再生障碍性贫血的有丝分裂相关药理机制
本研究的目的是从有丝分裂的角度研究改良的四味建中煎剂(SJD)对再生障碍性贫血(AA)的治疗作用及其潜在的药理机制。该研究采用网络药理学、萌芽随机化、分子对接和动物实验相结合的综合方法来评价石决明对再生障碍性贫血的作用。通过整合多个数据库,确定了 SJD 通过四个核心化合物(槲皮素、白藜芦醇、染料木素和姜黄素)靶向三个关键靶点[哺乳动物雷帕霉素靶点(MTOR)、聚(ADP-核糖)聚合酶 1(PARP1)和 Sirtuin 1(SIRT1)],对 AA 发挥治疗作用。孟德尔随机分析确定 MTOR 是 AA 发生的风险因素,而 PARP1 是保护因素。动物实验结果表明,SJD 可改善外周血计数,促进造血干细胞的增殖。从机理上讲,SJD(尤其是高剂量)通过激活有丝分裂相关蛋白PTEN诱导激酶1(PINK1)/Parkin和抑制磷脂酰肌醇3-激酶(PI3K)/蛋白激酶(AKT)/MTOR通路,对AA起到治疗作用。该研究首次揭示了SJD的核心化学成分及其对AA的药理作用,即通过激活有丝分裂来恢复造血功能。研究结果为中药在AA治疗中的临床应用提供了启示。
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来源期刊
Biomedical Chromatography
Biomedical Chromatography 生物-分析化学
CiteScore
3.60
自引率
5.60%
发文量
268
审稿时长
2.3 months
期刊介绍: Biomedical Chromatography is devoted to the publication of original papers on the applications of chromatography and allied techniques in the biological and medical sciences. Research papers and review articles cover the methods and techniques relevant to the separation, identification and determination of substances in biochemistry, biotechnology, molecular biology, cell biology, clinical chemistry, pharmacology and related disciplines. These include the analysis of body fluids, cells and tissues, purification of biologically important compounds, pharmaco-kinetics and sequencing methods using HPLC, GC, HPLC-MS, TLC, paper chromatography, affinity chromatography, gel filtration, electrophoresis and related techniques.
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