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Vasodilator-stimulated phosphoprotein protects against vascular inflammation and insulin resistance.

Vasodilator-stimulated phosphoprotein protects against vascular inflammation and insulin resistance.

Authors :
Cheng, Andrew M.
Rizzo-DeLeon, Norma
Wilson, Carole L.
Woo Je Lee
Tateya, Sanshiro
Clowes, Alexander W.
Schwartz, Michael W.
Kim, Francis
Source :
American Journal of Physiology: Endocrinology & Metabolism; Oct2014, Vol. 307 Issue 7, pE571-E579, 9p
Publication Year :
2014

Abstract

Among the pleotropic effects of endothelial nitric oxide (NO) is protection against vascular inflammation during high-fat diet (HFD) feeding. The current work investigated the role of the enzyme vasodilatory- stimulated phosphoprotein (VASP) as a downstream mediator of the anti-inflammatory effect of NO signaling in vascular tissue. Relative to mice fed a low-fat diet (LFD), levels of VASP Ser<superscript>239</superscript> phosphorylation, a marker of VASP activation, were dramatically reduced in aortic tissue of mice with obesity induced by consuming a HFD. As reported previously, the effect of the HFD was associated with increased aortic inflammation, as measured by increased N F - K B - dependent gene expression, and reduced vascular insulin sensitivity (including insulin-stimulated phosphorylation of eNOS and Akt). These effects of the HFD were recapitulated by VASP knockout, implying a physiological role for VASP to constrain inflammatory signaling and thereby maintain vascular insulin sensitivity. Conversely, overexpression of VASP in endothelial cells blocked inflammation and insulin resistance induced by palmitate. The finding that transplantation of bone marrow from VASP-deficient donors into normal recipients does not recapitulate the vascular effects of whole body VASP deficiency suggests that the protective effects of this enzyme are not mediated in immune or other bone marrow-derived cells. These studies implicate VASP as a downstream mediator of the NO/cGMP pathway that is both necessary and sufficient to protect against vascular inflammation and insulin resistance. As such, this work identifies VASP as a potential therapeutic target in the treatment of obesity-related vascular dysfunction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01931849
Volume :
307
Issue :
7
Database :
Complementary Index
Journal :
American Journal of Physiology: Endocrinology & Metabolism
Publication Type :
Academic Journal
Accession number :
98744695
Full Text :
https://doi.org/10.1152/ajpendo.00303.2014