Interventional effect of epalrestat on renal interstitial fibrosis in unilateral ureteral obstruction rats and its mechanism.
10.12047/j.cjap.5749.2019.019
- Author:
Yun-Xing GAO
1
;
Juan TANG
2
;
Qian ZHANG
2
;
Li-Li JIANG
2
;
Xian-Wei LI
3
,
4
Author Information
1. Departments of Medical Microbiology and Immunology, Wannan Medical College, Wuhu 241002.
2. Department of Pharmacology, Wannan Medical College.
3. Department of Pharmacology, Wannan Medical College
4. Anhui Provincial Engineering Technology Research Center for Polysaccharide Drugs, Wuhu 241002, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Enzyme Inhibitors;
pharmacology;
Fibrosis;
complications;
drug therapy;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Rhodanine;
analogs & derivatives;
pharmacology;
Thiazolidines;
pharmacology;
Ureteral Obstruction;
complications;
drug therapy
- From:
Chinese Journal of Applied Physiology
2019;35(1):79-84
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To observe the protective effects of epalrestat (EPS) on interstitial fibrosis in unilateral ureteral obstruction (UUO) rats and its mechanism.
METHODS:Rats were randomly divided into four groups: sham group, UUO group, UUO + epalrestat (50 or 100 mg/kg), 8 rats in each group.Rats in UUO and UUO + epalrestat group were obstructed left ureter.In the sham group, rats had their left ureters exposed and manipulated without ligation.Animals for epalrestat treatment received daily drug via gavage for 3 weeks, the rats of sham and UUO groups received equal amount of sodium carboxymethyl cellulose with the same regimen.Renal tissues pathological changes and collagen deposition were observed by HE and Masson's staining.The aldose reductase(AR) expression in renal tissues was measured by immunohistochemisty.The expression levels of collagen I, collagen III, alpha-smooth muscle actin (α-SMA), fibroblast-specific protein1 (FSP-1), fibronectin (FN), epithelial cadherin (E-cadherin), transforming growth factor-β1 (TGF-β1) and AR from kidney tissues were measured by real-time RT-PCR or Western blot.
RESULTS:Compared with the sham group, the renal tissues of the UUO group showed significant fibrosis, including renal tubular epithelial cell atrophy and vacuolated degeneration, collagen deposition, fibroblasts and myofibroblasts proliferation and inflammatory cell infiltration, and concomitantly with the expressions of collagen I, collagen III, TGF-β1, AR, α-SMA, FSP-1 and FN were remarkably up-regulated, but E-cadherin was significantly reduced in UUO group.Compared with the UUO group, after 3 weeks epalrestat administration, the level of renal interstitial fibrosis was obviously ameliorated and the expressions of collagen I, collagen III, TGF-β1, AR, α-SMA, FSP-1 and FN were remarkably down-regulated, but E-cadherin was significantly increased in rats of epalrestat groups.
CONCLUSION:These results suggest that epalrestat attenuates renal interstitial fibrosis possibly through inhibition of EMT via inhibiting TGF-β1 and AR expression.
