Submitted on February 3, 2009
Revised on May 26, 2009
Accepted on May 27, 2009
Periadventitial adipose tissue impairs coronary endothelial function via PKC-
dependent phosphorylation of nitric oxide synthase
Gregory A. Payne, H. Glenn Bohlen1, U. Deniz Dincer2, Lena Borbouse, and Johnathan D. Tune2*
1 Indiana University Medical School
2 Indiana University School of Medicine
* To whom correspondence should be addressed. E-mail: jtune{at}iupui.edu.
Endogenous periadventitial adipose-derived factors have been shown to contribute to coronary vascular regulation by impairing endothelial function through 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)-
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. Selective inhibition of endothelial PKC- with ruboxistaurin (1 µM) abolished adipose-induced impairment of bradykinin-mediated coronary vasodilation and 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 inhibition of PKC-. These data demonstrate that periadventitial adipose-derived factors impair coronary endothelial nitric oxide production via a PKC- dependent, site-specific phosphorylation of eNOS at Thr495.
