December 1997
Volume 38, Issue 13
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Articles  |   December 1997
Fluorophotometric quantitation of oxidative stress in the retina in vivo.
Author Affiliations
  • T Takanashi
    Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Kyoto University, Japan.
  • Y Ogura
    Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Kyoto University, Japan.
  • H Taguchi
    Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Kyoto University, Japan.
  • M Hashizoe
    Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Kyoto University, Japan.
  • Y Honda
    Department of Ophthalmology and Visual Sciences, Graduate School of Medicine, Kyoto University, Japan.
Investigative Ophthalmology & Visual Science December 1997, Vol.38, 2721-2728. doi:
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    • Get Citation

      T Takanashi, Y Ogura, H Taguchi, M Hashizoe, Y Honda; Fluorophotometric quantitation of oxidative stress in the retina in vivo.. Invest. Ophthalmol. Vis. Sci. 1997;38(13):2721-2728.

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

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Abstract

PURPOSE: To establish a new fluorophotometric method to quantitate oxidative stress in the retina in vivo with a hydrogen peroxide (H2O2)-sensitive fluorescent dye. METHODS: For in vitro fluorophotometric study, nonfluorescent 2',7'-dichlorofluorescein (DCFH) was incubated with H2O2 (10 pM to 100 nM), and the production of fluorescent 2',7'-dichlorofluorescein (DCF) was measured with fluorophotometric analysis. The inhibitory effect of catalase was also examined. For in vivo fluorophotometric study, rabbit eyes received vitrectomy and were perfused with 5 microM 2',7'-dichlorofluorescein diacetate (DCF-DA) or 2',7'-dichlorofluorescein diacetate (DCFH-DA). For oxidative stress, 300 microM H2O2 was infused after perfusion of DCFH-DA. Fluorophotometric measurements of the chorioretinal peak were performed. The eyes were enucleated for fluorescent microscopic examination to determine the localization of DCF fluorescence. RESULTS: H2O2 converted DCFH to DCF in a dose-dependent manner, which was inhibited by catalase dose dependently. In vivo fluorophotometric study showed DCF-DA and DCFH-DA caused production of 2006 +/- 274 picomole/ml (mean +/- SD, n = 5) and 8.35 +/- 1.11 picomole/ml (n = 5), respectively, in the chorioretinal peak. DCFH-DA with stimulation by H2O2 induced 30.7 +/- 13.1 (n = 4) picomole/ml DCF. Fluorescent microscopy showed DCF production in the retina was significant in the eye treated with DCF-DA and minimal in the eye treated with DCFH-DA. Moderate DCF production in the nerve fiber layer was observed in the eye treated with DCFH-DA and H2O2. CONCLUSIONS: This new fluorophotometric method with DCFH-DA may be useful in quantitatively evaluating oxidative stress in the retina in vivo.

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