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LTB4 promotes insulin resistance in obese mice by acting on macrophages, hepatocytes and myocytes.

Nature medicine | 2015

Insulin resistance results from several pathophysiologic mechanisms, including chronic tissue inflammation and defective insulin signaling. We found that liver, muscle and adipose tissue exhibit higher levels of the chemotactic eicosanoid LTB4 in obese high-fat diet (HFD)-fed mice. Inhibition of the LTB4 receptor Ltb4r1, through either genetic or pharmacologic loss of function, led to an anti-inflammatory phenotype with protection from insulin resistance and hepatic steatosis. In vitro treatment with LTB4 directly enhanced macrophage chemotaxis, stimulated inflammatory pathways, reduced insulin-stimulated glucose uptake in L6 myocytes, and impaired insulin-mediated suppression of hepatic glucose output in primary mouse hepatocytes. This was accompanied by lower insulin-stimulated Akt phosphorylation and higher Irs-1/2 serine phosphorylation, and all of these events were dependent on Gαi and Jnk1, two downstream mediators of Ltb4r1 signaling. These observations elucidate a novel role of the LTB4-Ltb4r1 signaling pathway in hepatocyte and myocyte insulin resistance, and they show that in vivo inhibition of Ltb4r1 leads to robust insulin-sensitizing effects.

Pubmed ID: 25706874 RIS Download

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Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: DK033651
  • Agency: NIDDK NIH HHS, United States
    Id: R24 DK090962
  • Agency: NIDDK NIH HHS, United States
    Id: P01 DK074868
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK033651
  • Agency: NIDDK NIH HHS, United States
    Id: DK09062
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK063491
  • Agency: NIDDK NIH HHS, United States
    Id: DK063491
  • Agency: NIDDK NIH HHS, United States
    Id: DK074868
  • Agency: NICHD NIH HHS, United States
    Id: P50 HD012303

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