Affiliation:
1. Division of Nephrology, Department of Medicine, Academic Medical Center, Amsterdam, The Netherlands
2. Department of Pathology, Academic Medical Center, Amsterdam, The Netherlands
3. Van Leeuwenhoek Center for Advanced Microscopy, Department of Cell Biology and Histology, Academic Medical Center, Amsterdam, The Netherlands
4. Tygat Institute for Liver and Intestinal Research, Amsterdam, The Netherlands
5. Dianet Foundation, Amsterdam-Utrecht, The Netherlands
Abstract
Introduction Chronic uremia and the exposure to dialysis solutions during peritoneal dialysis (PD) induce peritoneal alterations. Using a long-term peritoneal exposure model, we compared the effects of chronic kidney failure (CKD) itself and exposure to either a ‘conventional’ or a ‘biocompatible’ dialysis solution on peritoneal morphology and function. Methods Wistar rats (Harlan, Zeist, the Netherlands) were grouped into: normal kidney function (NKF), CKD induced by 70% nephrectomy, CKD receiving daily peritoneal infusions with 3.86% glucose Dianeal (CKDD), or Physioneal (both solutions from Baxter Healthcare, Castlebar, Ireland) (CKDP). At 16 weeks, a peritoneal function test was performed, and histology, ultrastructure, and hydroxyproline content of peritoneal tissue were assessed. Results Comparing CKD with NKF, peritoneal transport rates were higher, mesothelial cells (MC) displayed increased number of microvilli, blood and lymph vasculature expanded, vascular basal lamina appeared thicker, with limited areas of duplication, and fibrosis had developed. All alterations, except lymphangiogenesis, were enhanced by exposure to both dialysis fluids. Distinct MC alterations were observed in CKDD and CKDP, the latter displaying prominent basolateral protrusions. In addition, CKDP was associated with a trend towards less fibrosis compared to CKDD. Conclusions Chronic kidney failure itself induced peritoneal alterations, which were in part augmented by exposure to glucose-based dialysis solutions. Overall, the conventional and biocompatible solutions had similar long-term effects on the peritoneum. Importantly, the latter may attenuate the development of fibrosis.
Subject
Nephrology,General Medicine
Cited by
8 articles.
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1. Evaluation of peritoneal dialysis prescriptions in uremic rats;Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis;2023-08-17
2. Partial replacement ofd-glucose withd-allose ameliorates peritoneal injury and hyperglycaemia induced by peritoneal dialysis fluid in rats;Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis;2023-07-31
3. Long-Term Peritoneal Dialysis;Nolph and Gokal's Textbook of Peritoneal Dialysis;2023
4. Long-Term Peritoneal Dialysis;Nolph and Gokal's Textbook of Peritoneal Dialysis;2021
5. Therapeutic effect of 1,25(OH)2-VitaminD3 on fibrosis and angiogenesis of peritoneum induced by chlorhexidine;Biomedicine & Pharmacotherapy;2020-09