Nephrol Dial Transplant (2003) 18: 2629-2637
© 2003 European Renal Association-European Dialysis and Transplant Association
Original Article
Contribution of lactate buffer, glucose and glucose degradation products to peritoneal injury in vivo
1Department of Molecular Cell Biology, 3Department of Clinical Chemistry and 4Department of Nephrology, VU University Medical Center, Amsterdam and 2Baxter Healthcare, The Netherlands
Correspondence and offprint requests to: Jacob van den Born, Department of Molecular Cell Biology, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands. Email: j.vandenborn.cell{at}med.vu.nl
Background. Long-term peritoneal dialysis (PD) is associated with the development of functional and structural alterations of the peritoneal membrane. In this study, we investigated the contribution of low pH lactate buffer, high glucose concentration and glucose degradation products to peritoneal injury in a rat peritoneal exposure model.
Methods. Rats received daily 10 ml of either heat-sterilized (3.86% glucose, pH 5.2, n = 8) or filter-sterilized PD fluid (3.86% glucose, pH 5.2, n = 8), or lactate buffer (pH 5.2, n = 8) via a mini vascular access port during a 10 week period. Untreated rats served as controls.
Results. The low pH lactate buffer instillation induced pronounced morphological changes including the induction of angiogenesis in various peritoneal tissues and mild damage to the mesothelial cell layer covering the peritoneum. It also evoked a cellular response characterized by an increased mesothelial cell density on the liver, the induction of milky spots and accumulation of omental mast cells in the omentum, and significant changes in the composition of peritoneal leukocytes. The addition of glucose to low pH lactate buffer (filter-sterilized PD fluid) strengthened most, but not all of the responses described above and induced a fibrogenic response. In addition to glucose and low pH lactate buffer, the presence of glucose degradation products (heat-sterilized PD fluid) significantly induced an additional omental milky spot response (P < 0.03) and caused profound mesothelial damage. The vessel density in the omentum and the mesentery was significantly correlated to both the number of tissue mast cells and the hyaluronan content in the peritoneal lavage, which might suggest a role for mast cells and hyaluronan in the induction of angiogenesis.
Conclusions. Instillations of low pH lactate buffer, a high glucose concentration and glucose degradation products contribute differently and often cumulatively to peritoneal injury in vivo.
Keywords: CAPD; glucose degradation products; glucose; lactate buffer; peritoneal injury
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
P. Fabbrini, M. N. Schilte, M. Zareie, P. M. ter Wee, E. D. Keuning, R. H. J. Beelen, and J. van den Born Celecoxib treatment reduces peritoneal fibrosis and angiogenesis and prevents ultrafiltration failure in experimental peritoneal dialysis Nephrol. Dial. Transplant., August 7, 2009; (2009) gfp384v1. [Abstract] [Full Text] [PDF] |
||||
|
|
G. T. Gonzalez-Mateo, J. Loureiro, J. A. Jimenez-Hefferman, M.-A. Bajo, R. Selgas, M. Lopez-Cabrera, and L. S. Aroeira Chronic Exposure of Mouse Peritoneum to Peritoneal Dialysis Fluid: Structural and Functional Alterations of the Peritoneal Membrane Perit. Dial. Int., March 1, 2009; 29(2): 227 - 230. [Full Text] [PDF] |
||||
![]() |
K. Farhat, F. J. van Ittersum, P. M. ter Wee, and C. E. Douma Conventional versus biocompatible peritoneal dialysis fluids: more questions than answers? NDT Plus, October 1, 2008; 1(suppl_4): iv46 - iv50. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. T. Krediet, M. M. Zweers, R. van Westrhenen, A. Zegwaard, and D. G. Struijk Effects of reducing the lactate and glucose content of PD solutions on the peritoneum. Is the future GLAD? NDT Plus, October 1, 2008; 1(suppl_4): iv56 - iv62. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zareie, P. Fabbrini, L. H.P. Hekking, E. D. Keuning, P. M. ter Wee, R. H.J. Beelen, and J. van den Born Novel Role for Mast Cells in Omental Tissue Remodeling and Cell Recruitment in Experimental Peritoneal Dialysis J. Am. Soc. Nephrol., December 1, 2006; 17(12): 3447 - 3457. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zareie, E. D. Keuning, P. M. ter Wee, C. G. Schalkwijk, R. H. J. Beelen, and J. van den Born Improved biocompatibility of bicarbonate/lactate-buffered PDF is not related to pH Nephrol. Dial. Transplant., January 1, 2006; 21(1): 208 - 216. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zareie, G.-J. Tangelder, P. M. ter Wee, L. H. Hekking, A. A. van Lambalgen, E. D. Keuning, I. L. Schadee-Eestermans, C. G. Schalkwijk, R. H. Beelen, and J. van den Born Beneficial effects of aminoguanidine on peritoneal microcirculation and tissue remodelling in a rat model of PD Nephrol. Dial. Transplant., December 1, 2005; 20(12): 2783 - 2792. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zareie, A. S. De Vriese, L. H. P. Hekking, P. M. ter Wee, C. G. Schalkwijk, B. A. J. Driesprong, I. L. Schadee-Eestermans, R. H. J. Beelen, N. Lameire, and J. van den Born Immunopathological changes in a uraemic rat model for peritoneal dialysis Nephrol. Dial. Transplant., July 1, 2005; 20(7): 1350 - 1361. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zareie, E. D. Keuning, P. M. ter Wee, R. H. J. Beelen, and J. van den Born Peritoneal dialysis fluid-induced changes of the peritoneal membrane are reversible after peritoneal rest in rats Nephrol. Dial. Transplant., January 1, 2005; 20(1): 189 - 193. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Fusshoeller, M. Plail, B. Grabensee, and J. Plum Biocompatibility pattern of a bicarbonate/lactate-buffered peritoneal dialysis fluid in APD: a prospective, randomized study Nephrol. Dial. Transplant., August 1, 2004; 19(8): 2101 - 2106. [Abstract] [Full Text] [PDF] |
||||


