February 1995
Volume 36, Issue 2
Free
Articles  |   February 1995
Hydrogen peroxide affects specific epithelial subpopulations in cultured rabbit lenses.
Author Affiliations
  • J R Reddan
    Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4401.
  • F J Giblin
    Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4401.
  • D C Dziedzic
    Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4401.
  • B M Wirebaugh
    Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4401.
  • J L Peters
    Department of Biological Sciences, Oakland University, Rochester, Michigan 48309-4401.
Investigative Ophthalmology & Visual Science February 1995, Vol.36, 289-299. doi:
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    • Get Citation

      J R Reddan, F J Giblin, D C Dziedzic, B M Wirebaugh, J L Peters; Hydrogen peroxide affects specific epithelial subpopulations in cultured rabbit lenses.. Invest. Ophthalmol. Vis. Sci. 1995;36(2):289-299.

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

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Abstract

PURPOSE: To investigate the effect of hydrogen peroxide on the epithelial cells of cultured rabbit lenses. METHODS: Lenses were cultured in minimum essential medium containing a single dose of 0.03, 0.1, or 0.2 mM H2O2. Three hours later the medium was replaced with peroxide-free minimum essential medium. Lenses were also treated with 0.5 mM 1,3-bis(2-chloroethyl)-1 nitrosourea (BCNU) to lower the activity of glutathione reductase and then exposed to 0.03 mM H2O2 maintained nearly constant by glucose oxidase. After H2O2 treatment, lenses were fixed and whole mounts of the epithelium were prepared or lenses were processed for electron microscopy. RESULTS: Cells exposed to a single dose of 0.03 mM H2O2 appeared normal; 0.1 mM H2O2 was not cytotoxic. Exposure to 0.2 mM H2O2 elicited swelling in cells in the pre-equatorial region (30 minutes) followed by the formation of islands of cells in the pre-equatorial region at 1 hour. Central epithelial cells appeared normal at 1 hour, were swollen at 3 hours and dead at 24 hours. By 48 hours, dead cells were found in the pre-equatorial and central regions. Cells in the peripheral region of the epithelium did not exhibit cytotoxicity. If lenses were pretreated with BCNU and then challenged with a maintained level of 0.03 mM H2O2, cytotoxicity was induced in the central and pre-equatorial regions. Cells in the peripheral region survived BCNU-H2O2 treatment. CONCLUSIONS: Cells in the peripheral region of cultured lenses were more resistant to H2O2 cytotoxicity than cells in the central and pre-equatorial regions. The antioxidant defense or repair systems for H2O2-induced damage do not appear to be uniformly distributed in subpopulations of the lens epithelium.

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