Fish Oil Regulates Adiponectin Secretion by a Peroxisome Proliferator–Activated Receptor-γ–Dependent Mechanism in Mice

  1. Susanne Neschen12,
  2. Katsutaro Morino12,
  3. Jörg C. Rossbacher3,
  4. Rebecca L. Pongratz2,
  5. Gary W. Cline2,
  6. Saki Sono2,
  7. Matthew Gillum2 and
  8. Gerald I. Shulman12
  1. 1Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut
  2. 2Departments of Internal Medicine and Cellular & Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut
  3. 3Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut
  1. Address correspondence and reprint requests to Gerald I. Shulman, MD, PhD, Howard Hughes Medical Institute, Yale Medical School, P.O. Box 9812, New Haven, CT 06536-8012. E-mail: gerald.shulman{at}yale.edu

Abstract

Adiponectin has insulin-sensitizing, antiatherogenic, and anti-inflammatory properties, but little is known about factors that regulate its secretion. To examine the effect of fish oil on adiponectin secretion, mice were fed either a control diet or isocaloric diets containing 27% safflower oil or 27, 13.5, and 8% menhaden fish oil. Within 15 days, fish oil feeding raised plasma adiponectin concentrations two- to threefold in a dose-dependent manner, and the concentrations remained approximately twofold higher for 7 days when the fish oil diet was replaced by the safflower oil diet. Within 24 h, fish oil markedly induced transcription of the adiponectin gene in epididymal adipose tissue but not in subcutaneous fat. The increase of plasma adiponectin by fish oil was completely blocked by administration of the peroxisome proliferator–activated receptor (PPAR)γ inhibitor bisphenol-A-diglycidyl ether. In contrast, there was no effect of fish oil feeding on adiponectin secretion in PPARα-null mice. These data suggest that fish oil is a naturally occurring potent regulator of adiponectin secretion in vivo and that it does so through a PPARγ-dependent and PPARα-independent manner in epididymal fat.

Footnotes

  • S.N. and K.M. contributed equally to this study.

    S.N. is currently affiliated with the German Institute of Human Nutrition Potsdam, Nuthetal, Germany.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted January 3, 2006.
    • Received August 1, 2005.
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