Impaired insulin-mediated amino acid plasma disappearance in non-alcoholic fatty liver disease: a feature of insulin resistance

Dig Liver Dis. 2003 Oct;35(10):722-7. doi: 10.1016/s1590-8658(03)00416-x.

Abstract

Background and aim: Insulin resistance is a main feature, and possibly a pathogenic factor, of non-alcoholic fatty liver disease. It is usually measured on glucose metabolism; the effects on amino acid regulation have never been assessed. In particular, no data are available on insulin-dependent branched-chain amino acid metabolism, which is under insulin control.

Materials and methods: We measured amino acid disappearance from plasma during an euglycemic glucose clamp in 39 biopsy-proven non-alcoholic fatty liver disease patients and in ten control subjects. A primed-constant infusion of insulin (constant rate, 40 mU/m2 per min for 2 h) was used to raise plasma insulin to approximately 100 mU/l. Euglycemia was maintained by a variable glucose infusion, a measure of tissue insulin sensitivity. Plasma amino acids were assayed during the clamp after ninhidrin derivatization.

Results: Fasting plasma amino acids were similar in the two groups. Steady-state insulin levels were significantly higher in non-alcoholic fatty liver disease patients, whereas tissue sensitivity to insulin was reduced by 50%. The plasma disappearance of branched-chain amino acids, as well as the disappearance of the sum of glutamine and glutamate and that of serine were significantly reduced in non-alcoholic fatty liver disease. Differences were maintained after adjustment for steady-state insulin, and correlated with reduced tissue sensitivity to glucose.

Conclusion: Insulin resistance in non-alcoholic fatty liver disease patients also affects amino acid metabolism, especially for amino acids involved in peripheral muscle nitrogen exchange. The metabolic effects of altered protein/amino acid metabolism must be considered.

MeSH terms

  • Adult
  • Amino Acids / blood*
  • Amino Acids, Branched-Chain / blood
  • Blood Glucose / metabolism
  • Case-Control Studies
  • Fatty Liver / blood*
  • Fatty Liver / metabolism
  • Female
  • Glucose Clamp Technique
  • Humans
  • Insulin
  • Insulin Resistance*
  • Male

Substances

  • Amino Acids
  • Amino Acids, Branched-Chain
  • Blood Glucose
  • Insulin