12-Lipoxygenase-knockout mice are resistant to inflammatory effects of obesity induced by Western diet

Am J Physiol Endocrinol Metab. 2008 Nov;295(5):E1065-75. doi: 10.1152/ajpendo.90371.2008. Epub 2008 Sep 9.

Abstract

Inflammation is a key pathological process in the progression of atherosclerosis and type 2 diabetes. 12/15-lipoxygenase (12-LO), an enzyme involved in fatty acid metabolism, may contribute to inflammatory damage triggered by stressors such as obesity and insulin resistance. We hypothesized that mice lacking 12-LO are protected against inflammatory-mediated damage associated with a "western" diet. To test this hypothesis, age-matched male 12-LO knockout (12-LOKO) and wild-type C57BL/6 (B6) mice were fed either a standard chow or western diet and assessed for several inflammatory markers. Western-fed B6 mice showed expected reductions in glucose and insulin tolerance compared with chow-fed mice. In contrast, western-fed 12-LOKO mice maintained glucose and insulin tolerance similar to chow-fed mice. Circulating proinflammatory cytokines, tumor necrosis factor-alpha and interleukin-6, were increased in western B6 mice but not 12-LOKO mice, whereas the reported protective adipokine, adiponectin, was decreased only in western B6 mice. 12-LO activity was significantly elevated by western diet in islets from B6 mice. Islets from 12-LOKO mice did not show western-diet-induced islet hyperplasia or increases in caspase-3 apoptotic staining observed in western-fed B6 mice. Islets from 12-LOKO mice were also protected from reduced glucose-stimulated insulin secretion observed in islets from western-fed B6 mice. In visceral fat, macrophage numbers and monocyte chemoattractant protein-1 expression were elevated in western B6 mice but not 12-LOKO mice. These data suggest that 12-LO activation plays a role in western-diet-induced damage in visceral fat and islets. Inhibiting 12-LO may provide a new therapeutic approach to prevent inflammation-mediated metabolic consequences of excess fat intake.

Publication types

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

MeSH terms

  • Adipocytes, White / drug effects
  • Adipocytes, White / metabolism
  • Adipocytes, White / pathology
  • Adiponectin / blood
  • Adipose Tissue, White / drug effects
  • Adipose Tissue, White / metabolism
  • Adipose Tissue, White / pathology
  • Animals
  • Apoptosis / drug effects
  • Arachidonate 12-Lipoxygenase / genetics*
  • Arachidonate 12-Lipoxygenase / metabolism
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Chemokine CCL2 / metabolism
  • Cytokines / blood
  • Dietary Fats / administration & dosage
  • Dietary Fats / pharmacology
  • Glucose / pharmacology
  • Glucose Intolerance / blood
  • Inflammation / blood
  • Inflammation / etiology
  • Inflammation / pathology*
  • Insulin / blood
  • Insulin / metabolism
  • Insulin Resistance
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / pathology
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / pathology
  • Lipids / blood
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Obesity / blood
  • Obesity / etiology
  • Obesity / pathology*

Substances

  • Adiponectin
  • Adipoq protein, mouse
  • Blood Glucose
  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Cytokines
  • Dietary Fats
  • Insulin
  • Lipids
  • Arachidonate 12-Lipoxygenase
  • Glucose