Background. Long-term exposure to standard peritoneal dialysis fluid (PDF) results in alterations in peritoneal morphology and function. Studies investigating the long-term effects on the peritoneum of a low-glucose degradation product (GDP) bicarbonate/lactate-buffered PDF demonstrated its superior biocompatibility. We examined the potential of the low-GDP bicarbonate/lactate-buffered solution to reverse or reduce standard PDF-induced peritoneal alterations. Methods. Female Wistar rats received twice daily intraperitoneal infusions with either a lactate-buffered solution with 3.86% glucose at pH 5.5 (Dianeal®, referred to as standard PDF), or a low-GDP bicarbonate/lactate-buffered solution with 3.86% glucose at physiologic pH (Physioneal®, referred to as bicarbonate/lactate PDF) for different periods of time: (1) 12 weeks Dianeal® (N = 9); (2) 12 weeks Physioneal® (N = 9); (3) 20 weeks Dianeal® (N = 11); (4) 20 weeks Physioneal® (N = 10); (5) 12 weeks Dianeal® followed by 8 weeks Physioneal® (N = 10). Results. Chronic standard PDF exposure resulted in loss of ultrafiltration capacity, increased VEGF expression and vascular density, higher advanced glycation end product (AGE) accumulation, up-regulation of TGF-β expression, and development of fibrosis compared to low-GDP bicarbonate/lactate-buffered PDF. The PDF-induced alterations were time-dependent. Crossover from standard PDF to low-GDP bicarbonate/lactate PDF resulted in a less impaired ultrafiltration (UF), less pronounced VEGF expression and neoangiogenesis, and less severe AGE accumulation, TGF-β expression, and fibrosis compared to continuous standard PDF exposure for 20 weeks. Conclusion. Low-GDP bicarbonate/lactate- buffered PDF has the potential to slow down standard PDF-induced peritoneal membrane damage. © 2005 by the International Society of Nephrology.
CITATION STYLE
Mortier, S., Faict, D., Lameire, N. H., & De Vriese, A. S. (2005). Benefits of switching from a conventional to a low-GDP bicarbonate/lactate- buffered dialysis solution in a rat model. Kidney International, 67(4), 1559–1565. https://doi.org/10.1111/j.1523-1755.2005.00237.x
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