Insulin resistance is associated with higher intramyocellular triglycerides in type I but not type II myocytes concomitant with higher ceramide content

Diabetes. 2010 Jan;59(1):80-8. doi: 10.2337/db09-0988. Epub 2009 Oct 15.

Abstract

Objective: We tested the primary hypotheses that sphingolipid and diacylglycerol (DAG) content is higher within insulin-resistant muscle and that the association between intramyocellular triglycerides (IMTG) and insulin resistance is muscle fiber type specific.

Research design and methods: A nested case-control analysis was conducted in 22 obese (BMI >30 kg/m(2)) women who were classified as insulin-resistant (IR; n = 12) or insulin-sensitive (IS; n = 10), determined by hyperinsulinemic-euglycemic clamp (>30% greater in IS compared with IR, P < 0.01). Sphingolipid and DAG content was determined by high-performance liquid chromatography-tandem mass spectrometry. Fiber type-specific IMTG content was histologically determined. Gene expression was determined by quantitative PCR.

Results: Total (555 +/- 53 vs. 293 +/- 54 pmol/mg protein, P = 0.004), saturated (361 +/- 29 vs. 179 +/- 34 pmol/mg protein, P = 0.001), and unsaturated (198 +/- 29 vs. 114 +/- 21 pmol/mg protein, P = 0.034) ceramides were higher in IR compared with IS. DAG concentrations, however, were similar. IMTG content within type I myocytes, but not type II myocytes, was higher in IR compared with IS subjects (P = 0.005). Insulin sensitivity was negatively correlated with IMTG within type I myocytes (R = -0.51, P = 0.026), but not with IMTG within type II myocytes. The proportion of type I myocytes was lower (41 vs. 59%, P < 0.01) in IR subjects. Several genes involved in lipid droplet and fatty acid metabolism were differentially expressed in IR compared with IS subjects.

Conclusions: Human skeletal muscle insulin resistance is related to greater IMTG content in type I but not type II myocytes, to greater ceramide content, and to alterations in gene expression associated with lipid metabolism.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • Biopsy
  • Body Composition
  • Ceramides / metabolism*
  • Diglycerides / metabolism
  • Fatty Acids, Nonesterified / blood
  • Female
  • Gene Expression
  • Glyceraldehyde-3-Phosphate Dehydrogenases / genetics
  • Humans
  • Hypoxanthine Phosphoribosyltransferase / genetics
  • Insulin Resistance / physiology*
  • Muscle Cells / metabolism*
  • Muscle Cells / physiology
  • Muscle, Skeletal / physiology
  • Muscle, Skeletal / physiopathology
  • Polymerase Chain Reaction
  • RNA / genetics
  • Sphingolipids / metabolism
  • Triglycerides / metabolism*
  • beta 2-Microglobulin / genetics

Substances

  • Actins
  • Ceramides
  • Diglycerides
  • Fatty Acids, Nonesterified
  • Sphingolipids
  • Triglycerides
  • beta 2-Microglobulin
  • RNA
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Hypoxanthine Phosphoribosyltransferase