4.6 Article

Resveratrol Inhibits Pathologic Retinal Neovascularization in Vldlr-/- Mice

Journal

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
Volume 52, Issue 5, Pages 2809-2816

Publisher

ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/iovs.10-6496

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Funding

  1. Lowy Medical Foundation (MacTel)
  2. National Institutes of Health [EY017017, EY017017-S1, AG028730, AG027916]
  3. V. Kann Rasmussen Foundation
  4. Roche Foundation for Anemia Research
  5. CHB Mental Retardation and Developmental Disabilities Research Center
  6. RPB Senior Investigator Award
  7. Juvenile Diabetes Research Foundation International (JDRF)
  8. Knights Templar Eye Foundation
  9. Children's Hospital Boston Manton Center for Orphan Disease
  10. Deutsche Forschungsgemeinschaft
  11. Canadian Institutes of Health Research
  12. Canadian National Institute for the Blind
  13. Charles A. King Trust Award
  14. Juvenile Diabetes Research Foundation
  15. Glenn Foundation for Medical Research
  16. Ellison Medical Foundation

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PURPOSE. Macular telangiectasia (MacTel) is a vision-threatening retinal disease with unknown pathogenesis and no approved treatment. Very low-density lipoprotein receptor mutant mice (Vldlr(-/-)) exhibit critical features of MacTel such as retinal neovascularization and photoreceptor degeneration. In this study, the authors evaluate the therapeutic potential of resveratrol, a plant polyphenol, in Vldlr(-/-) mice as a model for MacTel. METHODS. Vldlr(-/-) and wild-type mice at postnatal day (P) 21 to P60 or P10 to P30 were treated orally with resveratrol. The number of neovascular lesions was evaluated on retinal flatmounts, and resveratrol effects on endothelial cells were assessed by Western blot for phosphorylated ERK1/2, aortic ring, and migration assays. Vegf and Gfap expression was evaluated in laser-capture microdissected retinal layers of angiogenic lesions and nonlesion areas from Vldlr(-/-) and wild-type retinas. RESULTS. From P15 onward, Vldlr(-/-) retinas develop vascular lesions associated with the local upregulation of Vegf in photoreceptors and Gfap in the inner retina. Oral resveratrol re-duces lesion formation when administered either before or after disease onset. The reduction of vascular lesions in resveratrol-treated Vldlr(-/-) mice is associated with the suppression of retinal Vegf transcription. Resveratrol also reduces endothelial ERK1/2 signaling as well as the migration and proliferation of endothelial cells. Furthermore, a trend toward increased rhodopsin mRNA in Vldlr(-/-) retinas is observed. CONCLUSIONS. Oral administration of resveratrol is protective against retinal neovascular lesions in Vldlr(-/-) mice by inhibiting Vegf expression and angiogenic activation of retinal endothelial cells. These results suggest that resveratrol might be a safe and effective intervention for treating patients with MacTel. (Invest Ophthalmol Vis Sci. 2011;52:2809-2816) DOI: 10.1167/iovs.10-6496

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