PDI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Perit Dial Int 18(3): 303-310 1998
© 1998 International Society for Peritoneal Dialysis
This Article
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Musi, B
Right arrow Articles by Rippe, B
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Musi, B
Right arrow Articles by Rippe, B
Peritoneal Dialysis International, Vol 18, Issue 3, 303-310
Copyright © 1998 by International Society for Peritoneal Dialysis


Articles

Effects of acidity, glucose degradation products, and dialysis fluid buffer choice on peritoneal solute and fluid transport in rats

B Musi, O Carlsson, A Rippe, A Wieslander, and B Rippe

Department of Nephrology and Physiology, University Hospital of Lund, Sweden.

OBJECTIVE: To evaluate the effects of acidity, glucose degradation products (GDP), and different solution buffer systems on solute and fluid transport during acute peritoneal dialysis (PD) in rats. DESIGN: Dialysis fluid (16 mL) containing 2.5% glucose as the osmotic agent was instilled intraperitoneally in Wistar rats (280 g) via a thin catheter in dwells lasting 4 hours. Blood and dialysis fluid samples (25 microL) were taken for measurement of glucose, sodium, and radioactive markers. The mass transfer area coefficient (MTAC or PS) for glucose and for 51Cr-EDTA (given as an intravenous infusion) and the peritoneal clearance (Cl) of 125I albumin (RISA), as well as the clearance of RISA to plasma (Cl --> P) were assessed for a commercial, heat-sterilized, acidic PD solution (2.5% glucose, pH 5.5; Gambrosol, Gambro, Lund, Sweden), containing GDP, and for four filter-sterilized solutions containing either lactate (40 mmol/L, pH 5.5 or 7.2), bicarbonate (38 mmol/L, pH 7.2), or pyruvate (40 mmol/L, pH 7.2) as buffers and being devoid of GDP. RESULTS: The initial pH of the acidic solutions increased rapidly, and attained physiological levels within 40 minutes. The initial drop of sodium, which is expected during the first part of the dwell, was significantly more pronounced with neutral than with acidic lactate. The PS for glucose and 51Cr-EDTA were slightly, but significantly, higher with the acidic and heat-sterilized solution (Gambrosol) than with the neutral, sterile-filtered lactate-buffered solution (p < 0.01), especially early during the dwell. Such an increase may be due to initial vasodilatation, and hence, recruitment of capillaries by the combination of acidity and GDP. However, there were no significant differences with respect to small solute PS values among sterile-filtered solutions, regardless of the presence of acidity or of buffer choice. CONCLUSION: There were no major differences in fluid and solute transport among sterile-filtered PD solutions having differing buffer systems and pH. Neither were there any effects of GDP alone. However, the combination of a low pH and the presence of GDP in the PD solutions seemed to cause significant increases in peritoneal small solute transport.




This article has been cited by other articles:


Home page
NDT PlusHome page
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]


Home page
Nephrol Dial TransplantHome page
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]


Home page
Nephrol Dial TransplantHome page
M. Zareie, L. H. P. Hekking, A. G. A. Welten, B. A. J. Driesprong, I. L. Schadee-Eestermans, D. Faict, A. Leyssens, C. G. Schalkwijk, R. H. J. Beelen, P. M. ter Wee, et al.
Contribution of lactate buffer, glucose and glucose degradation products to peritoneal injury in vivo
Nephrol. Dial. Transplant., December 1, 2003; 18(12): 2629 - 2637.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
S. Mortier, A. S. De Vriese, J. Van de Voorde, T. P. Schaub, J. Passlick-Deetjen, and N. H. Lameire
Hemodynamic Effects of Peritoneal Dialysis Solutions on the Rat Peritoneal Membrane: Role of Acidity, Buffer Choice, Glucose Concentration, and Glucose Degradation Products
J. Am. Soc. Nephrol., February 1, 2002; 13(2): 480 - 489.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
J. WITOWSKI, K. KORYBALSKA, J. WISNIEWSKA, A. BREBOROWICZ, G. M. GAHL, U. FREI, J. PASSLICK-DEETJEN, and A. JORRES
Effect of Glucose Degradation Products on Human Peritoneal Mesothelial Cell Function
J. Am. Soc. Nephrol., April 1, 2000; 11(4): 729 - 739.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Multimed Inc. logo
Copyright © 1998 by Multimed Inc.