Back to Search Start Over

l-Carnitine is an osmotic agent suitable for peritoneal dialysis

Authors :
Olivier Devuyst
Mario D’Arezzo
Yvette Cnops
Natalia Di Pietro
Lorenzo Di Liberato
Mario Bonomini
Sara Di Silvestre
Maria Pia Monaco
Annalisa Giardinelli
Pamela Di Tomo
Assunta Pandolfi
Arduino Arduini
Source :
Kidney International. 80:645-654
Publication Year :
2011
Publisher :
Elsevier BV, 2011.

Abstract

Excessive intraperitoneal absorption of glucose during peritoneal dialysis has both local cytotoxic and systemic metabolic effects. Here we evaluate peritoneal dialysis solutions containing L-carnitine, an osmotically active compound that induces fluid flow across the peritoneum. In rats, L-carnitine in the peritoneal cavity had a dose-dependent osmotic effect similar to glucose. Analogous ultrafiltration and small solute transport characteristics were found for dialysates containing 3.86% glucose, equimolar L-carnitine, or combinations of both osmotic agents in mice. About half of the ultrafiltration generated by L-carnitine reflected facilitated water transport by aquaporin-1 (AQP1) water channels of endothelial cells. Nocturnal exchanges with 1.5% glucose and 0.25% L-carnitine in four patients receiving continuous ambulatory peritoneal dialysis were well tolerated and associated with higher net ultrafiltration than that achieved with 2.5% glucose solutions, despite the lower osmolarity of the carnitine-containing solution. Addition of L-carnitine to endothelial cells in culture increased the expression of AQP1, significantly improved viability, and prevented glucose-induced apoptosis. In a standard toxicity test, the addition of L-carnitine to peritoneal dialysis solution improved the viability of L929 fibroblasts. Thus, our studies support the use of L-carnitine as an alternative osmotic agent in peritoneal dialysis.

Details

ISSN :
00852538
Volume :
80
Database :
OpenAIRE
Journal :
Kidney International
Accession number :
edsair.doi.dedup.....aeca2a256e1bff8cd7cefc50e76ab640
Full Text :
https://doi.org/10.1038/ki.2011.117