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Transgenic restoration of long-chain n-3 fatty acids in insulin target tissues improves resolution capacity and alleviates obesity-linked inflammation and insulin resistance in high-fat-fed mice.

Publication ,  Journal Article
White, PJ; Arita, M; Taguchi, R; Kang, JX; Marette, A
Published in: Diabetes
December 2010

OBJECTIVE: The catabasis of inflammation is an active process directed by n-3 derived pro-resolving lipid mediators. We aimed to determine whether high-fat (HF) diet-induced n-3 deficiency compromises the resolution capacity of obese mice and thereby contributes to obesity-linked inflammation and insulin resistance. RESEARCH DESIGN AND METHODS: We used transgenic expression of the fat-1 n-3 fatty acid desaturase from C. elegans to endogenously restore n-3 fatty acids in HF-fed mice. After 8 weeks on HF or chow diets, wild-type and fat-1 transgenic mice were subjected to insulin and glucose tolerance tests and a resolution assay was performed. Metabolic tissues were then harvested for biochemical analyses. RESULTS: We report that the n-3 docosanoid resolution mediator protectin D1 is lacking in muscle and adipose tissue of HF-fed wild-type mice. Accordingly, HF-fed wild-type mice have an impaired capacity to resolve an acute inflammatory response and display elevated adipose macrophage accrual and chemokine/cytokine expression. This is associated with insulin resistance and higher activation of iNOS and JNK in muscle and liver. These defects are reversed in HF-fed fat-1 mice, in which the biosynthesis of this important n-3 docosanoid resolution mediator is improved. Importantly, transgenic restoration of n-3 fatty acids prevented obesity-linked inflammation and insulin resistance in HF-fed mice without altering food intake, weight gain, or adiposity. CONCLUSIONS: We conclude that inefficient biosynthesis of n-3 resolution mediators in muscle and adipose tissue contributes to the maintenance of chronic inflammation in obesity and that these novel lipids offer exciting potential for the treatment of insulin resistance and diabetes.

Duke Scholars

Published In

Diabetes

DOI

EISSN

1939-327X

Publication Date

December 2010

Volume

59

Issue

12

Start / End Page

3066 / 3073

Location

United States

Related Subject Headings

  • Tumor Necrosis Factor-alpha
  • Obesity
  • Mice, Transgenic
  • Mice
  • Male
  • Lipids
  • Insulin Resistance
  • Inflammation
  • Fatty Acids, Omega-3
  • Fatty Acids
 

Citation

APA
Chicago
ICMJE
MLA
NLM
White, P. J., Arita, M., Taguchi, R., Kang, J. X., & Marette, A. (2010). Transgenic restoration of long-chain n-3 fatty acids in insulin target tissues improves resolution capacity and alleviates obesity-linked inflammation and insulin resistance in high-fat-fed mice. Diabetes, 59(12), 3066–3073. https://doi.org/10.2337/db10-0054
White, Phillip J., Makoto Arita, Ryo Taguchi, Jing X. Kang, and André Marette. “Transgenic restoration of long-chain n-3 fatty acids in insulin target tissues improves resolution capacity and alleviates obesity-linked inflammation and insulin resistance in high-fat-fed mice.Diabetes 59, no. 12 (December 2010): 3066–73. https://doi.org/10.2337/db10-0054.

Published In

Diabetes

DOI

EISSN

1939-327X

Publication Date

December 2010

Volume

59

Issue

12

Start / End Page

3066 / 3073

Location

United States

Related Subject Headings

  • Tumor Necrosis Factor-alpha
  • Obesity
  • Mice, Transgenic
  • Mice
  • Male
  • Lipids
  • Insulin Resistance
  • Inflammation
  • Fatty Acids, Omega-3
  • Fatty Acids