|  Help  |  About  |  Contact Us

Publication : Red wine polyphenol compounds favor neovascularisation through estrogen receptor α-independent mechanism in mice.

First Author  Chalopin M Year  2014
Journal  PLoS One Volume  9
Issue  10 Pages  e110080
PubMed ID  25299185 Mgi Jnum  J:223459
Mgi Id  MGI:5649179 Doi  10.1371/journal.pone.0110080
Citation  Chalopin M, et al. (2014) Red wine polyphenol compounds favor neovascularisation through estrogen receptor alpha-independent mechanism in mice. PLoS One 9(10):e110080
abstractText  Red wine polyphenol compounds (RWPC) exert paradoxical effects depending on the dose on post-ischemic neovascularisation. Low dose RWPC (0.2 mg/kg/day) is pro-angiogenic, whereas high dose (20 mg/kg/day) is anti-angiogenic. We recently reported that the endothelial effect of RWPC is mediated through the activation of a redox-sensitive pathway, mitochondrial biogenesis and the activation of alpha isoform of the estrogen receptor (ERalpha). Here, we investigated the implication of ERalpha on angiogenic properties of RWPC. Using ovariectomized mice lacking ERalpha treated with high dose of RWPC after hindlimb ischemia, we examined blood flow reperfusion, vascular density, nitric oxide (NO) production, expression and activation of proteins involved in angiogenic process and muscle energy sensing network. As expected, high dose of RWPC treatment reduced both blood flow and vascular density in muscles of mice expressing ERalpha. These effects were associated with reduced NO production resulting from diminished activity of eNOS. In the absence of RWPC, ERalpha deficient mice showed a reduced neo-vascularisation associated with a decreased NO production. Surprisingly in mice lacking ERalpha, high dose of RWPC increased blood flow and capillary density in conjunction with increased NO pathway and production as well as VEGF expression. Of particular interest is the activation of Sirt-1, AMPKalpha and PGC-1alpha/beta axis in ischemic hindlimb from both strains. Altogether, the results highlight a pro-angiogenic property of RWPC via an ERalpha-independent mechanism that is associated with an up-regulation of energy sensing network. This study brings a corner stone of a novel pathway for RWPC to correct cardiovascular diseases associated with failed neovascularisation.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

1 Bio Entities

0 Expression