Liu Jian, Liu Boning, Fan Enzhi, Zhang Han, Yin Zhonglai, Lv Shuquan, Wen Weibo, Min Feitian, Zhang Zhongyong, Cui Huantian
Department of Chinese Medicine, Cangzhou Hospital of Integrated Traditional Chinese Medicine and Western Medicine of Hebei, Cangzhou, China.
Department of Graduate School, Hebei University of Traditional Chinese Medicine, Shijiazhuang, China.
J Cell Mol Med. 2025 May;29(10):e70628. doi: 10.1111/jcmm.70628.
Diabetic nephropathy (DN) is a major complication of diabetes that can advance to end-stage renal disease, posing a substantial health risk. The Qianshi Mixture (QSM) has shown therapeutic potential for DN; however, its pharmacological mechanisms remain insufficiently understood. We developed a DN model in mice and administered QSM as an intervention. To assess QSM's therapeutic effects, we measured the renal-function-related biochemical indicators and examined kidney pathological changes. We then applied transcriptomics and non-targeted metabolomics to explore QSM's impact on gene expression and metabolic products within DN mice renal tissues. Based on our multi-omics analysis, the effect of QSM on lipid-metabolism-related protein expression was confirmed by western blot in kidney tissue. Additionally, we evaluated the antioxidant and anti-apoptotic properties of QSM by measuring oxidative stress indicators. QSM intervention improved hyperglycemia and proteinuria in DN mice. It also reduced key markers of renal dysfunction whilst alleviating pathological changes in kidney tissue. Through transcriptomic and metabolomic analyses, we identified that QSM affected genes and metabolites involved in lipid metabolism pathways. Notably, differentially expressed genes included Ces2h, Ces1f and Alox5, whilst metabolites such as EPA, 9-Oxo-ODE and LPC (20:3) were altered. Further validation revealed that QSM increased the protein levels of CES2H and CES1F whilst decreasing the expression of FABP1, CD36, ALOX15 and ALOX5. Additionally, QSM reduced oxidative stress markers. QSM inhibited both oxidative stress and apoptosis in kidney tissues. QSM protects renal tissues in DN, likely through the regulation of lipid metabolism and the mitigation of oxidative stress damage.
糖尿病肾病(DN)是糖尿病的一种主要并发症,可进展为终末期肾病,构成重大健康风险。芡实合剂(QSM)已显示出对DN的治疗潜力;然而,其药理机制仍未得到充分了解。我们在小鼠中建立了DN模型,并给予QSM作为干预措施。为了评估QSM的治疗效果,我们测量了肾功能相关的生化指标,并检查了肾脏病理变化。然后,我们应用转录组学和非靶向代谢组学来探索QSM对DN小鼠肾组织内基因表达和代谢产物的影响。基于我们的多组学分析,通过肾脏组织的蛋白质免疫印迹法证实了QSM对脂质代谢相关蛋白表达的影响。此外,我们通过测量氧化应激指标评估了QSM的抗氧化和抗凋亡特性。QSM干预改善了DN小鼠的高血糖和蛋白尿。它还降低了肾功能障碍的关键标志物,同时减轻了肾脏组织的病理变化。通过转录组学和代谢组学分析,我们确定QSM影响参与脂质代谢途径的基因和代谢产物。值得注意的是,差异表达基因包括Ces2h、Ces1f和Alox5,而代谢产物如EPA、9-氧代-十八碳二烯酸和溶血磷脂酰胆碱(20:3)发生了改变。进一步验证表明,QSM增加了CES2H和CES1F的蛋白水平,同时降低了FABP1、CD36、ALOX15和ALOX5的表达。此外,QSM降低了氧化应激标志物。QSM抑制了肾脏组织中的氧化应激和细胞凋亡。QSM可能通过调节脂质代谢和减轻氧化应激损伤来保护DN中的肾组织。