Peroxide-Induced Damage in Lenses of Transgenic Mice with Deficient and Elevated Levels of Glutathione Peroxidase
作者:
V.N. Reddy,
L.R. Lin,
Y.-S. Ho,
J.-L. Magnenat,
N. Ibaraki,
F.J. Giblin,
L. Dang,
期刊:
Ophthalmologica
(Karger Available online 1997)
卷期:
Volume 211,
issue 3
页码: 192-200
ISSN:0030-3755
年代: 1997
DOI:10.1159/000310788
出版商: S. Karger AG
关键词: Hydrogen peroxide;Glutathione peroxidase;Glutathione reductase;Transgenic mice;Lens epithelium;DNA strand breaks
数据来源: Karger
摘要:
Transgenic mice with elevated glutathione peroxidase (GSHPx) activity and gene knockout animals with a deficiency of the enzyme were used to investigate the role of GSHPx in defending the lens against H2O2-induced damage. The effects of peroxide on cultured lenses were determined by using light and transmission electron microscopy to evaluate morphological changes occurring in the epithelium and superficial cortex of the central and equatorial regions of the lens. DNA single-strand breaks in the epithelium were also examined. Following a 30-min exposure to 25 μM H2O2, lenses from normal animals showed distinct changes in the morphology of both the epithelium and superficial cortex. The damage to these cells was extensive in lenses of gene knockout mice in which activity of GSHPx was undetectable. In marked contrast, lenses of transgenic mice, which had 5-fold higher activities of GSHPx, were able to resist the cyto-toxic effects. Similar to damage to cell morphology, the extent of DNA strand breaks was significantly lower (40% of control) in H2O2-exposed lenses as compared to normal lenses while DNA damage in gene knockout lenses was 5 times greater than that of GSHPx-rich transgenic lenses. The present studies extend our previous findings on the role of the glutathione redox cycle in the detoxification of peroxide and demonstrate that an increase in GSHPx activity protects the lens against peroxide-induced changes in cell morphology and DNA strand breaks.
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