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Nephrol Dial Transplant ; 23(3): 991-7, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18045815

RESUMEN

BACKGROUND: Impaired protein anabolism and insulin resistance are characteristic features of maintenance haemodialysis patients. We have used a randomised, matched-paired, double-blind, placebo-controlled experimental design to determine the capability of intravenous L-carnitine supplementation to modify insulin resistance and protein catabolism in non-diabetic patients with end-stage renal disease (ESRD) undergoing chronic haemodialysis treatment. METHODS: L-carnitine (20 mg x kg(-1)) (n = 9) or placebo (n = 10) were given intravenously at the end of seven consecutive dialysis sessions. Whole-body protein and glucose metabolism were assessed on interdialytic days by the L[1-(13)C]leucine and the [2,2-(2)H(2)]glucose kinetic models in the postabsorptive state and during euglicemic hyperinsulinemic clamp studies at baseline and at the end of the treatment period. RESULTS: L-carnitine supplementation was associated with lower (P < 0.05) rates of leucine oxidation (-11 +/- 12%) and appearance from proteolysis (-6 +/- 2%) during the clamp studies than after placebo supplementation. The rates of glucose appearance in the postabsorptive state did not change significantly in the patients receiving L-carnitine treatment. Insulin-mediated glucose disappearance was improved by L-carnitine only in those patients (n = 5) (+18 +/- 3%, P < 0.05 vs placebo group, n = 5) with greater baseline insulin resistance, selected according to the median value of insulin sensitivity before treatment. CONCLUSIONS: L-carnitine supplementation was associated with protein-sparing effects in maintenance haemodialysis patients during hyperinsulinemia.


Asunto(s)
Carnitina/farmacología , Glucosa/metabolismo , Insulina/metabolismo , Fallo Renal Crónico/metabolismo , Fallo Renal Crónico/terapia , Proteínas/metabolismo , Diálisis Renal , Anciano , Carnitina/administración & dosificación , Método Doble Ciego , Femenino , Humanos , Inyecciones Intravenosas , Resistencia a la Insulina/fisiología , Leucina/metabolismo , Masculino , Persona de Mediana Edad
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