Therapeutic Effects of FK506 on IgA Nephropathy Rat

被引:8
|
作者
Wei, Linting [1 ]
Du, Yan [2 ]
Jia, Lining [1 ]
Ma, Xiaotao [1 ]
Chen, Zhao [1 ]
Lu, Jiamei [1 ]
Tian, Lifang [1 ]
Duan, Zhaoyang [1 ]
Dong, Fengming [3 ]
Lv, Zhian [1 ]
Yao, Ganglian [1 ]
Fu, Rongguo [1 ]
Wang, Li [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Nephrol, Xian 710004, Shaanxi, Peoples R China
[2] Xian Med Univ, Affiliated Hosp 1, Dept Nephrol, Xian, Shaanxi, Peoples R China
[3] Jiangsu Taizhou Peoples Hosp, Dept Nephrol, Taizhou, Peoples R China
来源
KIDNEY & BLOOD PRESSURE RESEARCH | 2017年 / 42卷 / 06期
基金
中国国家自然科学基金;
关键词
Fk506; IgA nephropathy; TRPC; Calcineurin; ERK1/2; REGULATED KINASES 1; CELL-PROLIFERATION; CYCLOSPORINE-A; GROWTH-FACTOR; URIC-ACID; CHANNELS; EXPRESSION; PROTEIN; ACTIVATION; ERK1/2;
D O I
10.1159/000485346
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Background/Aims: FK506 is an immunosuppressive drug and a calcineurin inhibitor that has been widely used in kidney disease in recent years. FK506 shows a wide range of biological and pharmaceutical effects; however, the mechanism of its anti-proliferative effect has not been well elucidated. An IgA nephropathy (IgAN) model was used to generate a mesangial cell proliferation model. This study aims to examine the effect of FK506 on IgAN rats and the underlying mechanisms. Methods: Hematuria, proteinuria and renal function were measured. To observe the pathological conditions, we performed HE (hematoxylin - eosin) and PAS (periodic acid - schiff) staining. Transcription and protein expression levels were detected by qRT - PCR (quantitative real-time polymerase chain reaction) and Wb (western blotting). The location and semi-quantitative expression levels of TRPCs, CaN (Calcineurin) and alpha-SMA were examined by IHC (Immunohistochemical staining). Results: We found that FK506 could improve hematuria, proteinuria and renal function, especially in the HF (high-dose FK506) groups. Renal pathological changes were ameliorated in the treatment groups. FK506 could significantly decrease TRPCs, CaN, phosphorylation of ERK1/2 and alpha-SMA expression. Conclusion: Taken together, these results suggest that the therapeutic effect of FK506 on IgAN might be partially associated with the down-regulated expression of TRPC channels, CaN and phosphorylation of ERK1/2. (c) 2017 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:983 / 998
页数:16
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