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This Article Full Text Full Text (PDF) All Versions of this Article: 291/5/E885    most recent 00109.2006v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (3) Citing Articles via Google Scholar Google Scholar Articles by Haider, D. G. Articles by Wolzt, M. Search for Related Content PubMed PubMed Citation Articles by Haider, D. G. Articles by Wolzt, M.

Free fatty acids normalize a rosiglitazone-induced visfatin release

¹Department of Clinical Pharmacology, ²Division of Endocrinology and Metabolism, Department of Internal Medicine III, and ³Department of Surgery, Medical University of Vienna; and ⁴Medical Department of Internal Medicine, Hanusch Hospital, Vienna, Austria

Submitted 8 March 2006 ; accepted in final form 26 May 2006

The detrimental effect of elevated free fatty acids (FFAs) on insulin sensitivity can be improved by thiazolidinediones (TZDs) in patients with type 2 diabetes mellitus. It is unknown whether this salutary action of TZD is associated with altered release of the insulin-mimetic adipocytokine visfatin. In this study, we investigated whether visfatin concentrations are altered by FFA and TZD treatment. In a randomized, double-blind, placebo-controlled, parallel-group study 16 healthy volunteers received an infusion of triglycerides/heparin to increase plasma FFA after 3 wk of treatment with rosiglitazone (8 mg/day, n = 8) or placebo (n = 8), and circulating plasma visfatin was measured. As a corollary, human adipocytes were incubated with synthetic fatty acids and rosiglitazone to assess visfatin release in vitro. The results were that rosiglitazone treatment increased systemic plasma visfatin concentrations from 0.6 ± 0.1 to 1.7 ± 0.2 ng/ml (P < 0.01). Lipid infusion caused a marked elevation of plasma FFA but had no effect on circulating visfatin in controls. In contrast, elevated visfatin concentrations in subjects receiving rosiglitazone were normalized by lipid infusion. In isolated adipocytes, visfatin was released into supernatant medium by acute addition and long-term treatment of rosiglitazone. This secretion was blocked by synthetic fatty acids and by inhibition of phosphatidylinositol 3-kinase or Akt. In conclusion, release of the insulin-mimetic visfatin may represent a major mechanism of metabolic TZD action. The presence of FFA antagonizes this action, which may have implications for visfatin bioactivity.

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				D. G. Haider, A. Handisurya, A. Storka, E. Vojtassakova, A. Luger, G. Pacini, A. Tura, M. Wolzt, and A. Kautzky-Willer Visfatin Response to Glucose Is Reduced in Women With Gestational Diabetes Mellitus Diabetes Care, July 1, 2007; 30(7): 1889 - 1891. [Full Text] [PDF]