Department of Hematology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang Province, China.
Biomed Chromatogr. 2024 Oct;38(10):e5963. doi: 10.1002/bmc.5963. Epub 2024 Jul 18.
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.
本研究旨在从自噬角度探讨十四味建中汤(SJD)治疗再生障碍性贫血(AA)的疗效及其潜在的药理机制。采用网络药理学、孟德尔随机化、分子对接和动物实验相结合的综合方法,评价 SJD 对 AA 的作用特性。通过整合多个数据库,确定 SJD 通过靶向三个关键靶点[雷帕霉素靶蛋白(MTOR)、多聚(ADP-核糖)聚合酶 1(PARP1)和 Sirtuin 1(SIRT1)],通过四种核心化合物(槲皮素、白藜芦醇、染料木黄酮和姜黄素)发挥对 AA 的治疗作用。孟德尔随机化分析表明,MTOR 是 AA 发生的危险因素,而 PARP1 是保护性因素。动物实验结果表明,SJD 可改善外周血象,促进造血干细胞增殖。机制上,SJD,特别是高剂量,通过激活与自噬相关的蛋白 PTEN 诱导激酶 1(PINK1)/Parkin 并抑制磷酸肌醇 3-激酶(PI3K)/蛋白激酶(AKT)/MTOR 通路发挥对 AA 的治疗作用。本研究首次揭示了 SJD 的核心化学成分及其对 AA 的药理作用,可通过激活自噬恢复造血功能。研究结果为中药在 AA 治疗中的临床应用提供了启示。