Insulin action on glucose and protein metabolism during L-carnitine supplementation in maintenance haemodialysis patients

Nephrol Dial Transplant. 2008 Mar;23(3):991-7. doi: 10.1093/ndt/gfm664. Epub 2007 Nov 28.

Abstract

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.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Carnitine / administration & dosage
  • Carnitine / pharmacology*
  • Double-Blind Method
  • Female
  • Glucose / metabolism*
  • Humans
  • Injections, Intravenous
  • Insulin / metabolism*
  • Insulin Resistance / physiology
  • Kidney Failure, Chronic / metabolism*
  • Kidney Failure, Chronic / therapy*
  • Leucine / metabolism
  • Male
  • Middle Aged
  • Proteins / metabolism*
  • Renal Dialysis*

Substances

  • Insulin
  • Proteins
  • Leucine
  • Glucose
  • Carnitine