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. 2021 Jan 29;4:144. doi: 10.1038/s42003-021-01652-x

Fig. 4. DPP4 deficiency, sitagliptin, and exendin-4 protected peritoneum against CG-inducing peritoneal fibrosis in rats.

Fig. 4

The experimental model of peritoneal fibrosis (PF) was established by chlorhexidine gluconate (CG) induction for 21 days in wild-type (i.e., Fischer 344) and DPP4 deficient (DPPD) rats. a Representative images of peritoneal tissue on day 21 were detected by immunofluorescent staining (200×) in SC-F344 (sham control, F344 wild type) and PF-F344 (peritoneal fibrosis, F344 wild type) rats for determining DPP4 (green color) and WT-1 positive signal (red color). DAPI labels cellular nuclei (blue color). b Histology of the peritoneum was observed by hematoxylin and eosin staining (H&E staining) in all the groups after CG-inducing PF. c Illustrating finding of Masson’s trichrome stain (200×) for identification of peritoneal fibrosis. d Quantitative result of peritoneal length by Masson’s trichrome stain in SC-F344, SC-DPP4D, PF-F344, and PF-DPP4D. e Quantitative result of peritoneal length by Masson’s trichrome stain in SC-F344, PF-F344, PF-F344 + Sita (sitagliptin), and PF-F344 + Exe4 (exendin-4). f, g Quantitative result of peritoneal area by Masson’s trichrome stain in each group. n = 6 for each group. Data represents the analysis and shows mean ± SD. Scale bars: 50 μm; HPF: high-power field. ** indicates p-value <0.01; *** represents p-value <0.001.