Polyunsaturated fatty acids of marine origin induce adiponectin in mice fed a high-fat diet
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Adiponectin biosynthesis blood genetics MeSH
- Enzyme Activation MeSH
- Dietary Fats administration & dosage pharmacology MeSH
- Glucose metabolism MeSH
- Insulin blood physiology MeSH
- Insulin Resistance MeSH
- Caloric Restriction MeSH
- AMP-Activated Protein Kinase Kinases MeSH
- Eicosapentaenoic Acid administration & dosage pharmacology MeSH
- Docosahexaenoic Acids administration & dosage pharmacology MeSH
- Leptin analysis blood genetics physiology MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Obesity physiopathology prevention & control MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Eating MeSH
- Protein Kinases metabolism MeSH
- Gene Expression Regulation MeSH
- Body Composition MeSH
- Triglycerides blood MeSH
- Adipose Tissue chemistry metabolism MeSH
- Adipocytes chemistry metabolism MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adiponectin MeSH
- Dietary Fats MeSH
- Glucose MeSH
- Insulin MeSH
- AMP-Activated Protein Kinase Kinases MeSH
- Eicosapentaenoic Acid MeSH
- Docosahexaenoic Acids MeSH
- Leptin MeSH
- Protein Kinases MeSH
- Triglycerides MeSH
AIMS/HYPOTHESIS: Diets rich in n-3 polyunsaturated fatty acids, namely eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), protect against insulin resistance and obesity in rodents and increase insulin sensitivity in healthy humans. We tested whether the anti-diabetic effects of EPA and DHA involve enhanced production of the endogenous insulin sensitiser, adiponectin. METHODS: We studied the effects, in an obesity-promoting high-fat diet, of partial replacement of vegetable oils by EPA/DHA concentrate (6% EPA, 51% DHA) over a 5-week period in adult male C57BL/6J mice that either had free access to food or had their food intake restricted by 30%. At the end of the treatment, systemic markers of lipid and glucose metabolism and full-length adiponectin and leptin were measured. Adiponectin (Adipoq) and leptin (Lep) gene expression in dorsolumbar and epididymal white adipose tissue (WAT) and isolated adipocytes was quantified and adipokine production from WAT explants evaluated. RESULTS: In mice with free access to food, plasma triacylglycerols, NEFA, and insulin levels were lower in the presence of EPA/DHA, while glucose and leptin levels were not significantly altered. Food restriction decreased plasma triacylglycerols, glucose, insulin and leptin, but not adiponectin. EPA/DHA increased plasma adiponectin levels, independent of food intake, reflecting the stimulation of Adipoq expression in adipocytes and the release of adiponectin from WAT, particularly from epididymal fat. Expression of Lep and the release of leptin from WAT, while being extremely sensitive to caloric restriction, was unaltered by EPA/DHA. CONCLUSIONS/INTERPRETATION: Intake of diets rich in EPA and DHA leads to elevated systemic concentrations of adiponectin, largely independent of food intake or adiposity and explain, to some extent, their anti-diabetic effects.
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