12-lipoxygenase promotes obesity-induced oxidative stress in pancreatic islets

Mol Cell Biol. 2014 Oct 1;34(19):3735-45. doi: 10.1128/MCB.00157-14. Epub 2014 Jul 28.

Abstract

High-fat diets lead to obesity, inflammation, and dysglycemia. 12-Lipoxygenase (12-LO) is activated by high-fat diets and catalyzes the oxygenation of cellular arachidonic acid to form proinflammatory intermediates. We hypothesized that 12-LO in the pancreatic islet is sufficient to cause dysglycemia in the setting of high-fat feeding. To test this, we generated pancreas-specific 12-LO knockout mice and studied their metabolic and molecular adaptations to high-fat diets. Whereas knockout mice and control littermates displayed identical weight gain, body fat distribution, and macrophage infiltration into fat, knockout mice exhibited greater adaptive islet hyperplasia, improved insulin secretion, and complete protection from dysglycemia. At the molecular level, 12-LO deletion resulted in increases in islet antioxidant enzymes Sod1 and Gpx1 in response to high-fat feeding. The absence or inhibition of 12-LO led to increases in nuclear Nrf2, a transcription factor responsible for activation of genes encoding antioxidant enzymes. Our data reveal a novel pathway in which islet 12-LO suppresses antioxidant enzymes and prevents the adaptive islet responses in the setting of high-fat diets.

Publication types

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

MeSH terms

  • Animals
  • Arachidonate 12-Lipoxygenase / genetics
  • Arachidonate 12-Lipoxygenase / metabolism*
  • Arachidonate 15-Lipoxygenase / genetics
  • Arachidonate 15-Lipoxygenase / metabolism*
  • Cytokines / metabolism
  • Diabetes Mellitus, Experimental / metabolism*
  • Diet, High-Fat / adverse effects*
  • Female
  • Gene Expression Regulation
  • Glucose Intolerance / metabolism
  • Glutathione Peroxidase / metabolism
  • Glutathione Peroxidase GPX1
  • Hyperplasia / pathology
  • Insulin-Secreting Cells / metabolism
  • Islets of Langerhans / metabolism*
  • Male
  • Mice
  • Mice, Knockout
  • NF-E2-Related Factor 2 / metabolism
  • Obesity / metabolism
  • Obesity / pathology*
  • Oxidative Stress*
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1

Substances

  • Cytokines
  • NF-E2-Related Factor 2
  • Glutathione Peroxidase
  • Alox15 protein, mouse
  • Arachidonate 12-Lipoxygenase
  • Arachidonate 15-Lipoxygenase
  • Sod1 protein, mouse
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • Glutathione Peroxidase GPX1
  • Gpx1 protein, mouse