The effects of mycophenolate mofetil on encapsulated peritoneal sclerosis model in rats


HÜR E., Bozkurt D., Timur O., Bicak S., Sarsik B., Akcicek F., ...More

Clinical Nephrology, vol.77, no.1, pp.1-7, 2012 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 77 Issue: 1
  • Publication Date: 2012
  • Doi Number: 10.5414/cn107140
  • Journal Name: Clinical Nephrology
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1-7
  • Keywords: Mycophenolate mofetil, Peritoneal sclerosis, Rat model
  • Uşak University Affiliated: No

Abstract

Introduction: Encapsulated peritoneal sclerosis (EPS) is a devastating complication of peritoneal dialysis. We aimed to investigate the effects of mycophenolate mofetil (MMF) treatment in experimental EPS in rats. Methods: 40 nonuremic Wistar albino rats were divided equally into 4 groups: control rats received 2 ml isotonic saline intraperitoneally daily for 3 weeks without any other treatment. The chlorhexidine gluconate group received intraperitoneally 2 ml/200 g injection of chlorhexidine gluconate and ethanol dissolved in saline for 3 weeks. The resting group received chlorhexidine gluconate (0 - 3 rd week) + peritoneal resting (4 th - 6 th week). The MMF group received chlorhexidine gluconate (0 - 3 rd week) + 125 mg/l MMF in drinking water (4 th - 6 th week). Dialysate cytokine levels, leukocyte count, peritoneal thickness, inflammation and fibroblast activities were evaluated. Results: Although the MMF and resting groups showed beneficial effects on ultrafiltration and D 1/D 0 glucose compared to the chlorhexidine gluconate group, only MMF treatment improved dialysate TGF-β1, VEGF and MCP-1 levels compared to the resting group. Inflammatory activity and vascularity observed in a tissue biopsy, including capillaries number per mm 2 of submesothelial area, decreased in the treatment group. Conclusions: MMF treatment has beneficial effects on EPS via inhibiting inflammation and neovascularisation by reducing dialysate VEGF overexpression. © 2012 Dustri-Verlag Dr. K. Feistle.