12/15-lipoxygenase is required for the early onset of high fat diet-induced adipose tissue inflammation and insulin resistance in mice

PLoS One. 2009 Sep 29;4(9):e7250. doi: 10.1371/journal.pone.0007250.

Abstract

Background: Recent understanding that insulin resistance is an inflammatory condition necessitates searching for genes that regulate inflammation in insulin sensitive tissues. 12/15-lipoxygenase (12/15LO) regulates the expression of proinflammatory cytokines and chemokines and is implicated in the early development of diet-induced atherosclerosis. Thus, we tested the hypothesis that 12/15LO is involved in the onset of high fat diet (HFD)-induced insulin resistance.

Methodology/principal findings: Cells over-expressing 12/15LO secreted two potent chemokines, MCP-1 and osteopontin, implicated in the development of insulin resistance. We assessed adipose tissue inflammation and whole body insulin resistance in wild type (WT) and 12/15LO knockout (KO) mice after 2-4 weeks on HFD. In adipose tissue from WT mice, HFD resulted in recruitment of CD11b(+), F4/80(+) macrophages and elevated protein levels of the inflammatory markers IL-1beta, IL-6, IL-10, IL-12, IFNgamma, Cxcl1 and TNFalpha. Remarkably, adipose tissue from HFD-fed 12/15LO KO mice was not infiltrated by macrophages and did not display any increase in the inflammatory markers compared to adipose tissue from normal chow-fed mice. WT mice developed severe whole body (hepatic and skeletal muscle) insulin resistance after HFD, as measured by hyperinsulinemic euglycemic clamp. In contrast, 12/15LO KO mice exhibited no HFD-induced change in insulin-stimulated glucose disposal rate or hepatic glucose output during clamp studies. Insulin-stimulated Akt phosphorylation in muscle tissue from HFD-fed mice was significantly greater in 12/15LO KO mice than in WT mice.

Conclusions: These results demonstrate that 12/15LO mediates early stages of adipose tissue inflammation and whole body insulin resistance induced by high fat feeding.

Publication types

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

MeSH terms

  • Adipose Tissue / metabolism*
  • Animal Feed
  • Animals
  • Arachidonate 12-Lipoxygenase / metabolism
  • Arachidonate 12-Lipoxygenase / physiology*
  • Arachidonate 15-Lipoxygenase / metabolism
  • Arachidonate 15-Lipoxygenase / physiology*
  • CD11b Antigen / biosynthesis
  • Crosses, Genetic
  • Dietary Fats / metabolism*
  • Humans
  • Inflammation
  • Insulin / metabolism
  • Insulin Resistance*
  • Male
  • Mice
  • Mice, Knockout
  • beta-Galactosidase / metabolism

Substances

  • 12-15-lipoxygenase
  • CD11b Antigen
  • Dietary Fats
  • Insulin
  • Arachidonate 12-Lipoxygenase
  • Arachidonate 15-Lipoxygenase
  • beta-Galactosidase