Tan Zhuojing, Si Yachen, Yu Yan, Ding Jiarong, Huang Linxi, Xu Ying, Zhang Hongxia, Lu Yihan, Wang Chao, Yu Bing, Yuan Li
Department of Nephrology, Affiliated Hospital of Nantong University, Nantong, China.
Department of Cell Biology, Naval Medical University (Second Military Medical University), Shanghai, China.
Front Pharmacol. 2022 Jun 15;13:917428. doi: 10.3389/fphar.2022.917428. eCollection 2022.
Focal segmental glomerulosclerosis (FSGS) is a common clinical condition with manifestations of nephrotic syndrome and fibrosis of the glomeruli and interstitium. Yi-Shen-Hua-Shi (YSHS) granule has been shown to have a good effect in alleviating nephrotic syndrome (NS) in clinical and in animal models of FSGS, but whether it can alleviate renal fibrosis in FSGS and its mechanism and targets are not clear. In this study, we explored the anti-fibrotic effect and the targets of the YSHS granule in an adriamycin (ADR)-induced FSGS model and found that the YSHS granule significantly improved the renal function of ADR-induced FSGS model mice and also significantly reduced the deposition of collagen fibers and the expression of mesenchymal cell markers FN, vimentin, and α-SMA in the glomeruli of ADR-induced FSGS mice, suggesting that the YSHS granule inhibited the fibrosis of sclerotic glomeruli. Subsequently, a network pharmacology-based approach was used to identify the potential targets of the YSHS granule for the alleviation of glomerulosclerosis in FSGS, and the results showed that the YSHS granule down-regulated the expressions of BMP2, GSTA1, GATS3, BST1, and S100A9 and up-regulated the expressions of TTR and GATM in ADR-induced FSGS model mice. We also proved that the YSHS granule inhibited the fibrosis in the glomeruli of ADR-induced FSGS model mice through the suppression of the BMP2/Smad signaling pathway.
局灶节段性肾小球硬化(FSGS)是一种常见的临床病症,表现为肾病综合征以及肾小球和间质纤维化。益肾化湿颗粒(YSHS)在临床和FSGS动物模型中已显示出对缓解肾病综合征(NS)有良好效果,但它是否能缓解FSGS中的肾纤维化及其机制和靶点尚不清楚。在本研究中,我们在阿霉素(ADR)诱导的FSGS模型中探讨了YSHS颗粒的抗纤维化作用及其靶点,发现YSHS颗粒显著改善了ADR诱导的FSGS模型小鼠的肾功能,还显著减少了ADR诱导的FSGS小鼠肾小球中胶原纤维的沉积以及间充质细胞标志物FN、波形蛋白和α-SMA的表达,表明YSHS颗粒抑制了硬化肾小球的纤维化。随后,采用基于网络药理学的方法来确定YSHS颗粒缓解FSGS中肾小球硬化的潜在靶点,结果显示YSHS颗粒下调了ADR诱导的FSGS模型小鼠中BMP2、GSTA1、GATS3、BST1和S100A9的表达,并上调了TTR和GATM的表达。我们还证明YSHS颗粒通过抑制BMP2/Smad信号通路抑制了ADR诱导的FSGS模型小鼠肾小球中的纤维化。