Effects of meal ingestion on intramyocellular ceramide concentrations and fractional de novo synthesis in humans

Am J Physiol Endocrinol Metab. 2018 Feb 1;314(2):E105-E114. doi: 10.1152/ajpendo.00153.2017. Epub 2017 Sep 26.

Abstract

We investigated the effects of meal ingestion on intramyofibrillar (IMF) and subsarcolemmal (SS) ceramide metabolism in volunteers ranging from lean to obese. Thirty-eight women and men underwent a steady-state meal ingestion protocol that included a 6.5-h infusion of [U-13C]palmitate and muscle biopsies 1.5 and 6.5 h after starting the tracer infusion. We measured IMF and SS sphingolipid concentrations and the contribution of plasma palmitate to intramyocellular C16:0 ceramide by use of LC-MS-MS. In response to meal ingestion SS C24 ceramide concentrations, but not C14-C20 concentrations, increased significantly. IMF ceramide concentrations did not change. The increases in SS C24 ceramides were negatively related to parameters of insulin resistance. The fractional contribution of plasma palmitate to intramyocellular C16:0 ceramides in both IMF and SS fractions was inversely related to overweight status (β = -0.432, P = 0.0095 and β = -0.443, P = 0.0058, respectively). These data indicate that meal ingestion has differing effects on SS ceramide subspecies and suggest that the fractional de novo synthesis of intramyocellular ceramide from plasma palmitate in the postprandial condition is reduced in those who are overweight.

Keywords: insulin resistance; isotopic tracers; meals; obesity; skeletal muscle.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Biopsy
  • Body Composition
  • Ceramides / metabolism*
  • Chemical Fractionation
  • Eating / physiology*
  • Female
  • Humans
  • Lipid Metabolism
  • Male
  • Meals / physiology*
  • Muscle Fibers, Skeletal / chemistry
  • Muscle Fibers, Skeletal / metabolism*
  • Muscle Fibers, Skeletal / pathology
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • Obesity / metabolism
  • Obesity / pathology
  • Young Adult

Substances

  • Ceramides