Systemic regulation of L-carnitine in nutritional metabolism in zebrafish, Danio rerio

Sci Rep. 2017 Jan 19:7:40815. doi: 10.1038/srep40815.

Abstract

Excess fat accumulation has been observed widely in farmed fish; therefore, efficient lipid-lowering factors have obtained high attention in the current fish nutrition studies. Dietary L-carnitine can increase fatty acid β-oxidation in mammals, but has produced contradictory results in different fish species. To date, the mechanisms of metabolic regulation of L-carnitine in fish have not been fully determined. The present study used zebrafish to investigate the systemic regulation of nutrient metabolism by dietary L-carnitine supplementation. L-carnitine significantly decreased the lipid content in liver and muscle, accompanied by increased concentrations of total and free carnitine in tissues. Meanwhile, L-carnitine enhanced mitochondrial β-oxidation activities and the expression of carnitine palmitoyltransferase 1 mRNA significantly, whereas it depressed the mRNA expression of adipogenesis-related genes. In addition, L-carnitine caused higher glycogen deposition in the fasting state, and increased and decreased the mRNA expressions of gluconeogenesis-related and glycolysis-related genes, respectively. L-carnitine also increased the hepatic expression of mTOR in the feeding state. Taken together, dietary L-carnitine supplementation decreased lipid deposition by increasing mitochondrial fatty acid β-oxidation, and is likely to promote protein synthesis. However, the L-carnitine-enhanced lipid catabolism would cause a decrease in glucose utilization. Therefore, L-carnitine has comprehensive effects on nutrient metabolism in fish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carnitine / metabolism
  • Carnitine / pharmacology*
  • Carnitine O-Palmitoyltransferase / genetics
  • Carnitine O-Palmitoyltransferase / metabolism
  • Dietary Supplements
  • Gluconeogenesis / genetics
  • Glycogen / metabolism
  • Glycolysis / genetics
  • Lipid Metabolism / drug effects*
  • Lipid Peroxidation / drug effects
  • Liver / metabolism
  • Mitochondria / metabolism
  • Muscles / metabolism
  • TOR Serine-Threonine Kinases / metabolism
  • Zebrafish / metabolism*

Substances

  • Glycogen
  • Carnitine O-Palmitoyltransferase
  • TOR Serine-Threonine Kinases
  • Carnitine