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


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

Clinical Nephrology, cilt.77, sa.1, ss.1-7, 2012 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 77 Sayı: 1
  • Basım Tarihi: 2012
  • Doi Numarası: 10.5414/cn107140
  • Dergi Adı: Clinical Nephrology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1-7
  • Anahtar Kelimeler: Mycophenolate mofetil, Peritoneal sclerosis, Rat model
  • Uşak Üniversitesi Adresli: Hayır

Özet

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.