June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
Anti-angiogenic Effects of Doxazosin on Experimental Choroidal Neovascularization in Mice
Author Affiliations & Notes
  • Wei Liu
    Shanghai First People's Hospital, Shanghai, Shanghai, China
  • Jiaxian Guo
    Shanghai First People's Hospital, Shanghai, Shanghai, China
  • Xiaodong Sun
    Shanghai First People's Hospital, Shanghai, Shanghai, China
  • Footnotes
    Commercial Relationships   Wei Liu, None; Jiaxian Guo, None; Xiaodong Sun, None
  • Footnotes
    Support  National Natural Science Foundation of China(81425006)
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 4073. doi:
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    • Get Citation

      Wei Liu, Jiaxian Guo, Xiaodong Sun; Anti-angiogenic Effects of Doxazosin on Experimental Choroidal Neovascularization in Mice
      . Invest. Ophthalmol. Vis. Sci. 2017;58(8):4073.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : The present study was designed to evaluate the effects of doxazosin on experimental choroidal neovascularization (CNV) in mice.

Methods : Six-to eight-week-old male C57BL/6 mice were divided into a control group and a doxazosin-treated group (5 mg/kg, i.p., daily). Experimental CNV was induced by laser photocoagulation. 7 days and 14 days after laser induction, fluorescein angiography, choroidal flat mounts and histological studies were performed to evaluate the fluorescence leakage, area and thickness of CNV lesions, respectively. In addition, western blot analysis was carried out to assess the inhibitory effects of doxazosin on the PI3K/Akt/mTOR signaling pathway and the expression levels of HIF-1α and VEGF, which are involved in CNV model.

Results : Compared with the control group, the doxazosin-treated group demonstrated significantly less fluorescence leakage on day 7 and day 14 after laser induction. Both the area and the thickness of CNV lesions in the doxazosin-treated group were significantly decreased. Mechanistically, PI3K/Akt/mTOR signaling pathway activation was significantly suppressed in the doxazosin-treated group. The expression of HIF-1α and VEGF was also notably reduced by systemic doxazosin treatment.

Conclusions : Doxazosin exerts anti-angiogenic actions in an experimental mouse model of CNV and may be a potential adjunctive therapy for neovascular age-related macular degeneration in humans.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.

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