Scutellarin ameliorates diabetic nephropathy via TGF-β1 signaling pathway

被引:0
|
作者
Huang, Bangrui [1 ,2 ]
Han, Rui [1 ]
Tan, Hong [1 ]
Zhu, Wenzhuo [1 ]
Li, Yang [1 ]
Jiang, Fakun [2 ]
Xie, Chun [2 ]
Ren, Zundan [1 ]
Shi, Rou [1 ]
机构
[1] Kunming Med Univ, Dept Endocrinol, Affiliated Hosp 1, Kunming 650032, Peoples R China
[2] Yunnan Univ, Yunnan Prov Ctr Res & Dev Nat Prod, Sch Pharm, Key Lab Med Chem Nat Resource,Minist Educ, Kunming 650500, Peoples R China
关键词
Scutellarin; Diabetic nephropathy; Proteinuria; Fibrosis; Podocyte injury; MOLECULAR-MECHANISMS; KIDNEY-DISEASE; TGF-BETA/SMAD; PODOCYTE; BREVISCAPINE; FIBROSIS; BETA;
D O I
10.1007/s13659-024-00446-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Breviscapine, a natural flavonoid mixture derived from the traditional Chinese herb Erigeron breviscapus (Vant.) Hand-Mazz, has demonstrated a promising potential in improving diabetic nephropathy (DN). However, the specific active constituent(s) responsible for its therapeutic effects and the underlying pharmacological mechanisms remain unclear. In this study, we aimed to investigate the impact of scutellarin, a constituent of breviscapine, on streptozotocin-induced diabetic nephropathy and elucidate its pharmacological mechanism(s). Our findings demonstrate that scutellarin effectively ameliorates various features of DN in vivo, including proteinuria, glomerular expansion, mesangial matrix accumulation, renal fibrosis, and podocyte injury. Mechanistically, scutellarin appears to exert its beneficial effects through modulation of the transforming growth factor-beta 1 (TGF-beta 1) signaling pathway, as well as its interaction with the extracellular signal-regulated kinase (Erk) and Wnt/beta-catenin pathways.
引用
收藏
页数:11
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