Yu Xinxin, Pu Xing, Xi Yu, Li Xiang, Jiang Wei, Chen Xiaoling, Xu Yong, Xie Juan, Li Hailun, Zheng Donghui
Department of Nephrology, Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, Jiangsu, 223002, PR China.
Heliyon. 2024 Aug 2;10(16):e35489. doi: 10.1016/j.heliyon.2024.e35489. eCollection 2024 Aug 30.
Treating kidney diseases from the perspective of spleen is an important clinical method in traditional Chinese medicine (TCM) for anti-renal fibrosis (RF). Si-jun-zi decoction (SJZD), a classic formula for qi-invigorating and spleen-invigorating, has been reported to alleviate RF. This study aims to investigate the potential mechanism by which SJZD attenuates RF. The results demonstrated notable improvements in renal function levels, inflammation and fibrosis indices in UUO-mice following SJZD intervention. The main active ingredients identified were Quercetin, Kaempferol, Naringenin and 7-Methoxy-2-methyl isoflavone. Furthermore, STAT3, MAPK3, MYC were confirmed as key targets. Additionally, GO enrichment analysis demonstrated that SJZD delayed RF primarily by regulating oxidative stress and other biological mechanisms. KEGG enrichment analysis revealed the involvement of pathways such as Lipid and atherosclerosis signaling pathway, MAPK signaling pathway and other pathways in the reno-protective effects of SJZD. The molecular docking results revealed that the active ingredients of SJZD were well-bound and stable to the core targets. The experiments results revealed that Quercetin, Kaempferol, and Naringenin not only improved the morphology of TGF-β-induced HK-2 cells but also reversed the expression of α-SMA, COL1A1 and MAPK, thereby delaying the progression of RF. The anti-RF effects of SJZD were exerted through multi-components, multi-targets and multi-pathways.
从脾论治肾病是中医抗肾纤维化的重要临床方法。四君子汤(SJZD)是一种经典的益气健脾方剂,据报道可减轻肾纤维化。本研究旨在探讨SJZD减轻肾纤维化的潜在机制。结果表明,SJZD干预后,UUO小鼠的肾功能水平、炎症和纤维化指标有显著改善。鉴定出的主要活性成分有槲皮素、山柰酚、柚皮素和7-甲氧基-2-甲基异黄酮。此外,STAT3、MAPK3、MYC被确认为关键靶点。另外,GO富集分析表明,SJZD主要通过调节氧化应激等生物学机制延缓肾纤维化。KEGG富集分析显示,脂质和动脉粥样硬化信号通路、MAPK信号通路等通路参与了SJZD的肾保护作用。分子对接结果表明,SJZD的活性成分与核心靶点结合良好且稳定。实验结果显示,槲皮素、山柰酚和柚皮素不仅改善了TGF-β诱导的HK-2细胞的形态,还逆转了α-SMA、COL1A1和MAPK的表达,从而延缓了肾纤维化的进展。SJZD的抗肾纤维化作用是通过多成分、多靶点和多途径发挥的。