4.6 Article

Adiponectin translation is increased by the PPARγ agonists pioglitazone and ω-3 fatty acids

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.90892.2008

Keywords

peroxisome proliferator-activated receptor-gamma; translational regulation; adipocyte biology; ribonucleic acid-binding proteins; fish oils; thiazolidinediones

Funding

  1. Veterans Administration
  2. American Diabetes Association
  3. National Institute of Diabetes and Digestive and Kidney Diseases [DK-39176, DK-080327]

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Banga A, Unal R, Tripathi P, Pokrovskaya I, Owens RJ, Kern PA, Ranganathan G. Adiponectin translation is increased by the PPAR gamma agonists pioglitazone and omega-3 fatty acids. Am J Physiol Endocrinol Metab 296: E480-E489, 2009. First published December 16, 2008; doi:10.1152/ajpendo.90892.2008.-Adiponectin, made exclusively by adipocytes, is a 30-kDa secretory protein assembled posttranslationally into low-molecular weight, middle-molecular weight, and high-molecular weight homo-oligomers. PPAR gamma ligand thiozolidinediones, which are widely used in the treatment of type II diabetes, increase adiponectin levels. PPAR gamma also has several putative ligands that include fatty acid derivatives. Overnight treatment of rat adipocytes with pioglitazone, docosahexaenoic acid (DHA), or eicosapentaenoic acid (EPA) triggered a twofold increase in the synthesis and secretion of HMW adiponectin, and this increase was blocked by the addition of PPAR gamma inhibitor GW-9662. Inhibition of glycosylation using 2,2'-dipyridyl decreased the synthesis of high-molecular weight adiponectin by pioglitazone, EPA, and DHA, but there was increased secretion of trimeric adiponectin resulting from increased translation. Although pioglitazone, DHA, and EPA increased adiponectin synthesis by more than 60%, there was no increase in total protein synthesis and no corresponding change in adiponectin mRNA expression, indicating the upregulation of translation. We examined the possibility of transacting factors in the cytoplasmic extracts from adipocytes treated with pioglitazone or DHA. In vitro translation of adiponectin mRNA was inhibited by S-100 fraction of control adipocytes and increased by S-100 extracts from adipocytes treated with pioglitazone or DHA. Consistent with this observation, both pioglitazone and DHA treatments increased the association of adiponectin mRNA with the heavier polysome fractions. Together, these data suggest that pioglitazone and the fish oils DHA or EPA are PPAR gamma agonists in adipocytes with regard to adiponectin expression, and the predominant mode of adiponectin stimulation is via an increase in translation.

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