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10.3389/fphar.2017.00780

http://scihub22266oqcxt.onion/10.3389/fphar.2017.00780
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C5672017!5672017!29163166
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suck abstract from ncbi


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pmid29163166      Front+Pharmacol 2017 ; 8 (ä): ä
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  • Saxagliptin Attenuates Albuminuria by Inhibiting Podocyte Epithelial- to-Mesenchymal Transition via SDF-1? in Diabetic Nephropathy #MMPMID29163166
  • Chang Yp; Sun B; Han Z; Han F; Hu Sl; Li Xy; Xue M; Yang Y; Chen L; Li Cj; Chen Lm
  • Front Pharmacol 2017[]; 8 (ä): ä PMID29163166show ga
  • The dipeptidyl peptidase-4 (DPP-4) inhibitor saxagliptin has been found to reduce progressive albuminuria, but the exact mechanism of inhibition is unclear. Podocyte epithelial-to-mesenchymal transition (EMT) has emerged as a potential pathway leading to proteinuria in diabetic nephropathy (DN). Stromal cell?derived factor-1? (SDF-1?), one of the substrates of DPP-4, can activate the protein kinase A pathway and subsequently inhibit its downstream effector, transforming growth factor-?1 (TGF-?1), which induces podocyte EMT. Thus, this study was designed to test the hypothesis that saxagliptin reduces progressive albuminuria by preventing podocyte EMT through inhibition of SDF-1? cleavage in DN. The results of a series of assays, including ELISA, western blotting, and immunochemistry/immunofluorescence, showed that saxagliptin treatment obviously ameliorated urinary microalbumin excretion and renal histological changes in high-fat diet/streptozotocin-induced diabetic rats. Furthermore, saxagliptin-treated diabetic rats presented with suppression of DPP-4 activity/protein expression accompanied by restoration of SDF-1? levels, which subsequently hindered NOX2 expression and podocyte EMT. In vitro, we consistently observed that saxagliptin significantly inhibited increased DPP-4 activity/expression, oxidative stress and podocyte EMT. Application of an SDF-1? receptor inhibitor (AMD3100) to cultured podocytes further confirmed the essential role of SDF-1? in podocyte EMT inhibition. In sum, we demonstrated for the first time that saxagliptin treatment plays an essential role in ameliorating progressive DN by preventing podocyte EMT through a SDF-1?-related pathway, suggesting that saxagliptin could offer renoprotection and that SDF-1? might be a potential therapeutic target for DN.
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