中国医科大学学报2025，Vol.54Issue(9)：769-774,780,7.DOI:10.12007/j.issn.0258-4646.2025.09.001
毛蕊花糖苷在糖尿病肾病中的保护作用及机制
Protective effect and mechanism of acteoside in diabetic nephropathy
摘要
Abstract
Objective To investigate the effects of acteoside in a rat model on of diabetic nephropathy(DN)and high-glucose-induced glomerular mesangial cells(GMCs),focusing on the role of acteoside in the silent information regulator 1(SIRT1)/nuclear factor eryth-roid 2-related factor 2(Nrf2)signaling pathway.Methods GMCs were cultured under normal glucose conditions or stimulated with high glucose.Fibrosis,oxidative stress,SIRT1 and Nrf2 protein expression,and mitochondrial structure were assessed in four groups:normal glucose,high glucose,high glucose+acteoside,and high glucose+acteoside+SIRT1 inhibitor(hsa62).DN was induced in rats via intraperitoneal streptozotocin injection,and animals were divided into control,model,and acteoside-treated groups.Pathological kidney changes,blood glucose changes,renal function indices,and protein expression of SIRT1 and Nrf2 were evaluated.Results Compared with controls,DN model rats showed significantly elevated fasting blood glucose,serum creatinine,blood urea nitrogen,and 24-h urinary protein levels of rats in the model group were significantly increased(P＜0.01).GMCs exhibited increased fibrosis,oxidative stress,and mitochondrial damage.Acteoside treatment significantly improved all measured parameters(P＜0.01);and mitigated mitochondrial injury.In vitro,acteoside reduced high-glucose-induced fibrosis and oxidative stress in GMCs,effects that were reversed by SIRT1 inhibition.Western blotting confirmed upregulation of SIRT1 and Nrf2 expression in both treated rat kidney tissues and GMCs(P＜0.01).Conclusion Acteoside alleviates glomerular fibrosis and oxidative stress in DN by activating the SIRT1/Nrf2 signaling pathway,suggesting its potential therapeutic agent for DN.关键词
毛蕊花糖苷/糖尿病肾病/肾小球系膜细胞Key words
acteoside/diabetic nephropathy/glomerular mesangial cell分类
医药卫生引用本文复制引用
王冬燕,郭兆安,唐静楠,刘慧,苏珊珊..毛蕊花糖苷在糖尿病肾病中的保护作用及机制[J].中国医科大学学报,2025,54(9):769-774,780,7.基金项目
山东省自然科学基金(ZR2022LZY005) （ZR2022LZY005）
