4.4 Article

Anti-angiogenic actions of the mangosteen polyphenolic xanthone derivative α-mangostin

Journal

MICROVASCULAR RESEARCH
Volume 93, Issue -, Pages 72-79

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mvr.2014.03.005

Keywords

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Funding

  1. Ministry of Science and Technology, Thailand
  2. Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Biomedical Laboratory Research and Development (VA) [BX001233]
  3. National Institutes of Health (NIH) [R01-EY11766]
  4. Culver Vision Discovery Institute at Georgia Regents University [BX001233]

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Retinal neovascularization is a major cause of vision loss in diseases characterized by retinal ischemia and is characterized by the pathological growth of abnormal vessels. Vascular endothelial growth factor (VEGF) is known to play an important role in this process. Oxidative stress has been strongly implicated in up-regulation of VEGF associated with neovascularization in various tissues. Hence, compounds with anti-oxidant actions can prevent neovascularization. alpha-Mangostin, a component of mangosteen (Garcinia mangostana Linn), has been shown to have an anti-oxidant property in pathological conditions involving angiogenesis such as cancer. However, the effect of alpha-mangostin on ROS formation and angiogenic function in microvascular endothelial cells has not been studied. Hence, this study demonstrated the anti-angiogenic effects of alpha-mangostin in relation to ROS formation in bovine retinal endothelial cells (REC). alpha-Mangostin significantly and dose-dependently reduced formation of ROS in hypoxia-treated REC. alpha-Mangostin also significantly and dose-dependently suppressed VEGF-induced increases in permeability, proliferation, migration and tube formation in REC and blocked angiogenic sprouting in the ex vivo aortic ring assay. In addition, alpha-mangostin inhibited VEGF-induced phosphorylation of VEGFR2 and ERK1/2-MAPK. According to our results, alpha-mangostin reduces oxidative stress and limits VEGF-induced angiogenesis through a process involving abrogation of VEGFR2 and ERK1/2-MAPK activation. (C) 2014 Elsevier Inc All rights reserved.

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