Curcumin mediates repulsive guidance molecule B (RGMb) in the treatment mechanism of renal fibrosis induced by unilateral ureteral obstruction

被引:15
作者
Chen, Fei [1 ]
Xie, Yu [1 ]
Lv, Qin [1 ]
Zou, Wei [2 ]
Xiong, Liyan [1 ]
机构
[1] Kunming Univ Sci & Technol, Peoples Hosp Yunnan Prov 1, Affiliated Hosp, Dept Nephrol, 157 Jinbi Rd, Kunming 650032, Yunnan, Peoples R China
[2] Nanchang Univ, Nanchang, Jiangxi, Peoples R China
关键词
Curcumin; Dragon; renal fibrosis; unilateral ureteral obstruction; repulsive guidance molecule B; GROWTH-FACTOR-BETA; TGF-BETA; EXPRESSION; CANCER; BETA/SMAD; GENE;
D O I
10.1080/0886022X.2021.1997764
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
In this study, we explored the role and mechanism of repulsive guidance molecule B (RGMb, also known as Dragon) in the protective effects of curcumin against renal fibrosis and verified Dragon's effect on renal tubular epithelial cell apoptosis and cell programmability. Unilateral ureteral obstruction (UUO) was surgically induced in rats to establish a model of renal interstitial fibrosis (RIF). The rats were then treated with curcumin. Curcumin prominently decreased the serum creatinine (SCr) and blood urea nitrogen (BUN) levels, and also improved the tubular injury in the UUO-induced rats. Curcumin significantly downregulated the TGF-beta 1, P-Smad2/3, cleaved caspase-3, cleaved caspase-8 and Dragon levels. Dragon knockdown also markedly reduced the TGF-beta 1, P-Smad2/3, Smad2/3, cleaved caspase-3, cleaved caspase-8, fibronectin, collagen I, collagen IV, vimentin, and alpha-SMA expression levels. Conversely, Dragon overexpression caused higher expression levels of these proteins, and curcumin reversed this effect. Furthermore, Dragon knockdown increased the E-cadherin levels, whereas Dragon overexpression decreased these levels. Overexpressing Dragon significantly decreased the cell viability, and curcumin reversed this effect. In conclusion, curcumin acted on Dragon and attenuated RIF in UUO rat models. Curcumin downregulated the TGF-beta 1/Smad signaling pathway and inhibited Dragon and fibrogenic molecules in both rats and HK-2 cells.
引用
收藏
页码:1496 / 1505
页数:10
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