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Clinical |
1 Institut National de la Transfusion Sanguine; 2 INSERM, U665;3 Université Paris 7-Denis Diderot, UFR Médecine, Paris; 4 Fresenius Medical Care, Fresnes; 5 Clinique de Néphrologie, Centre Hospitalier Régional Universitaire, Lille, France
Correspondence to: E. Boulanger, Laboratoire de Biologie Vasculaire et
Cellulaire, Institut National de la Transfusion Sanguine, 6 Rue A. Cabanel,
75739 Paris, Cedex 15,
France.
dreboulanger{at}hotmail.com
Background: Conventional peritoneal dialysis fluids (PDFs)
have been shown to damage the mesothelial layer and are associated with the
development of peritoneal fibrosis and neoangiogenesis. New-generation PDFs
have therefore been developed with physiological pH and reduced levels of
glucose degradation products (GDPs), precursors of advanced glycation end
products (AGEs). In this work, we evaluated and compared the improved
biocompatibility of two new-generation PDFs (Balance and bicaVera) using
mesothelial cell biology; we also compared them to a standard PDF
(stay·safe) (all PDFs by Fresenius Medical Care, Fresnes, France).
Methods: stay·safe, Balance, and bicaVera were
tested for their effect on human peritoneal mesothelial cell (HPMC) viability
by measuring cell proliferation and apoptosis, and oncosis induction. The
formation of AGEs was evaluated by immunoassay. Transforming growth factor
beta-1 and vascular endothelial growth factor (VEGF) were immunoassayed in
HPMC supernatants exposed to the above PDFs.
Results: At 15 g/L glucose concentration, HPMC exposure to
bicaVera resulted in higher cell proliferation compared to Balance (p
< 0.001) and stay·safe (p < 0.001). Compared to the
lactate-buffered PDFs (Balance and stay·safe), oncosis was
significantly lower in cells exposed to bicaVera (p < 0.05).
bicaVera, containing lower amounts of GDPs, generated less AGE formation
(p < 0.05) and VEGF production (p < 0.05) than either
Balance or stay·safe.
Conclusions: New-generation PDFs with physiological pH and
lower GDP levels, especially if bicarbonate-buffered (bicaVera), have fewer
in vitro toxic effects on mesothelial cells and may contribute to
peritoneal preservation, thus improving long-term treatment of PD
patients.
KEY WORDS: Glycoxidation; biocompatibility; mesothelial cell.
Received 21 December 2005; accepted 22 April 2006.
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