Open Access

Sitagliptin ameliorates diabetic nephropathy by blocking TGF-β1/Smad signaling pathway

  • Authors:
    • Dongdong Wang
    • Guanying Zhang
    • Xiao Chen
    • Tong Wei
    • Chenxu Liu
    • Chun Chen
    • Yinhan Gong
    • Qunli Wei
  • View Affiliations

  • Published online on: February 16, 2018     https://doi.org/10.3892/ijmm.2018.3504
  • Pages: 2784-2792
  • Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Diabetic nephropathy (DN) is the leading cause of end-stage failure of the kidney, but the efficacy of current strategies available for the prevention of DN remains unsatisfactory. The purpose of this study was to assess whether sitagliptin (SIT) has therapeutic potential for prevention of DN and to investigate its possible mechanism. The effects of SIT on DN were investigated in rats with type 2 diabetes mellitus (T2DM) and rat mesangial cells (MCs) induced by high glucose. T2DM rats were administered at a dose of 10 mg/kg SIT. The kidney index, 24 h urinary protein, blood urea nitrogen (BUN), serum creatinine (Cr), accumulation of glycogen and collagens were investigated by different methods. MCs were administered with SIT at doses of 0.1, 1 and 10 µmol/ml. The possible mechanism of SIT on protection of diabetic kidney injury was examined by expression of transforming growth factor-β1 (TGF-β1)/Smad pathway. The results showed that the SIT-treated diabetic rats significantly reduced diabetic kidney injury by inhibiting the kidney index and attenuating 24 h urinary protein, reducing BUN and serum creatinine, inhibiting progressive renal fibrosis and increassing extracellular matrix including collagen IV and fibronectin. Further studies showed that inhibition of renal fibrosis in SIT-treated diabetic rats and MCs were associated with rebalancing of TGF-β1/Smad pathway. Sitagliptin may be a potent agent for preventing the progression of DN through inhabiting TGF-β1/Smad-mediated renal fibrosis.
View Figures
View References

Related Articles

Journal Cover

May-2018
Volume 41 Issue 5

Print ISSN: 1107-3756
Online ISSN:1791-244X

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Wang D, Zhang G, Chen X, Wei T, Liu C, Chen C, Gong Y and Wei Q: Sitagliptin ameliorates diabetic nephropathy by blocking TGF-β1/Smad signaling pathway. Int J Mol Med 41: 2784-2792, 2018
APA
Wang, D., Zhang, G., Chen, X., Wei, T., Liu, C., Chen, C. ... Wei, Q. (2018). Sitagliptin ameliorates diabetic nephropathy by blocking TGF-β1/Smad signaling pathway. International Journal of Molecular Medicine, 41, 2784-2792. https://doi.org/10.3892/ijmm.2018.3504
MLA
Wang, D., Zhang, G., Chen, X., Wei, T., Liu, C., Chen, C., Gong, Y., Wei, Q."Sitagliptin ameliorates diabetic nephropathy by blocking TGF-β1/Smad signaling pathway". International Journal of Molecular Medicine 41.5 (2018): 2784-2792.
Chicago
Wang, D., Zhang, G., Chen, X., Wei, T., Liu, C., Chen, C., Gong, Y., Wei, Q."Sitagliptin ameliorates diabetic nephropathy by blocking TGF-β1/Smad signaling pathway". International Journal of Molecular Medicine 41, no. 5 (2018): 2784-2792. https://doi.org/10.3892/ijmm.2018.3504