L-Carnitine is an osmotic agent suitable for peritoneal dialysis

被引:32
作者
Bonomini, Mario [1 ]
Pandolfi, Assunta [2 ]
Di Liberato, Lorenzo [1 ]
Di Silvestre, Sara [2 ]
Cnops, Yvette [3 ,4 ]
Di Tomo, Pamela [2 ]
D'Arezzo, Mario [1 ]
Monaco, Maria P. [1 ]
Giardinelli, Annalisa [2 ]
Di Pietro, Natalia [2 ]
Devuyst, Olivier [3 ,4 ]
Arduini, Arduino
机构
[1] Univ G DAnnunzio, Dept Med, Inst Nephrol, Chieti, Italy
[2] Univ G DAnnunzio, Dept Biomed Sci, Aging Res Ctr, CeSI,G dAnnunzio Univ Fdn, Chieti, Italy
[3] Catholic Univ Louvain, Sch Med, Div Nephrol, B-1200 Brussels, Belgium
[4] CoreQuest Sagl, Dept Res & Dev, Tecnopolo, Bioggio, Switzerland
关键词
endothelium; fibroblast; peritoneal dialysis; ultrafiltration; water channels; NITRIC-OXIDE SYNTHASE; MEMBRANE; GLUCOSE; AQUAPORIN-1; APOPTOSIS; ULTRAFILTRATION; FLUID; METABOLISM; EXPRESSION; ICODEXTRIN;
D O I
10.1038/ki.2011.117
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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 dosedependent 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. Kidney International (2011) 80, 645-654; doi: 10.1038/ki.2011.117; published online 27 April 2011
引用
收藏
页码:645 / 654
页数:10
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