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This Article Full Text Full Text (PDF) All Versions of this Article: 297/1/H460    most recent 00116.2009v1 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 PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Payne, G. A. Articles by Tune, J. D. PubMed PubMed Citation Articles by Payne, G. A. Articles by Tune, J. D.

Periadventitial adipose tissue impairs coronary endothelial function via PKC-β-dependent phosphorylation of nitric oxide synthase

¹Department of Cellular and Integrative Physiology and ²Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana

Submitted 3 February 2009 ; accepted in final form 27 May 2009

Endogenous periadventitial adipose-derived factors have been shown to contribute to coronary vascular regulation by impairing endothelial function through a direct inhibition of endothelial nitric oxide synthase (eNOS). However, our understanding of the underlying mechanisms remains uncertain. Accordingly, this study was designed to test the hypothesis that periadventitial adipose tissue releases agents that attenuate coronary endothelial nitric oxide production via a protein kinase C (PKC)-β-dependent mechanism. Isometric tension studies were conducted on isolated canine circumflex coronary arteries with and without natural amounts of periadventitial adipose tissue. Adipose tissue significantly diminished coronary endothelial-dependent vasodilation and nitric oxide production in response to bradykinin and acetylcholine. The selective inhibition of endothelial PKC-β with ruboxistaurin (1 µM) abolished the adipose-induced impairment of bradykinin-mediated coronary vasodilation and the endothelial production of nitric oxide. Western blot analysis revealed a significant increase in eNOS phosphorylation at the inhibitory residue Thr⁴⁹⁵ in arteries exposed to periadventitial adipose tissue. This site-specific phosphorylation of eNOS was prevented by the inhibition of PKC-β. These data demonstrate that periadventitial adipose-derived factors impair coronary endothelial nitric oxide production via a PKC-β-dependent, site-specific phosphorylation of eNOS at Thr⁴⁹⁵.

coronary circulation; adipokine; endothelial nitric oxide synthase; protein kinase C-β