Reactive oxygen species (ROS)-generating oxidases in the normal rabbit cornea and their involvement in the corneal damage evoked by UVB rays
Jazyk angličtina Země Španělsko Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
11332708
DOI
10.14670/hh-16.523
Knihovny.cz E-zdroje
- MeSH
- alkoholoxidoreduktasy metabolismus účinky záření MeSH
- časové faktory MeSH
- histocytochemie MeSH
- inhibitory enzymů farmakologie MeSH
- králíci MeSH
- oxidasa D-aminokyselin metabolismus účinky záření MeSH
- reaktivní formy kyslíku metabolismus MeSH
- rohovka enzymologie účinky záření MeSH
- rohovkový endotel cytologie enzymologie patologie MeSH
- rohovkový epitel cytologie enzymologie patologie MeSH
- scavengery volných radikálů farmakologie MeSH
- senzitivita a specificita MeSH
- ultrafialové záření škodlivé účinky MeSH
- xanthinoxidasa metabolismus účinky záření MeSH
- zvířata MeSH
- Check Tag
- králíci MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- alkoholoxidoreduktasy MeSH
- inhibitory enzymů MeSH
- L-2-hydroxyacid oxidase MeSH Prohlížeč
- oxidasa D-aminokyselin MeSH
- reaktivní formy kyslíku MeSH
- scavengery volných radikálů MeSH
- xanthinoxidasa MeSH
The corneas of albino rabbits were irradiated (5 min exposure once a day) with UVB rays (312 nm) for 4 days (shorter procedure) or 8 days (longer procedure). The eyes were examined microbiologically and only the corneas of sterile eyes or eyes with non-pathogenic microbes were employed. Histochemically, the activities of reactive oxygen species (ROS)-generating oxidases (xanthine oxidase, D-amino acid oxidase and alpha-hydroxy acid oxidase) were examined in cryostat sections of the whole corneas. Biochemically, the activity of xanthine oxidoreductase/xanthine oxidase was investigated in the scraped corneal epithelium. UVB rays significantly changed enzyme activities in the corneas. In comparison to the normal cornea, where of ROS-generating oxidases only xanthine oxidase showed significant activity in the corneal epithelium and endothelium, D-amino acid oxidase was very low and alpha-hydroxy acid oxidase could not be detected at all, in the cornea repeatedly irradiated with UVB rays, increased activities of xanthine oxidase and D-amino acid oxidase were observed in all corneal layers. Only after the longer procedure the xanthine oxidase and D-amino acid oxidase activities were decreased in the thinned epithelium in parallel with its morphological disturbances. Further results show that the xanthine oxidase/xanthine oxidoreductase ratio increased in the epithelium together with the repeated irradiation with UVB rays. This might suggest that xanthine dehydrogenase is converted to xanthine oxidase. However, in comparison to the normal corneal epithelium, the total amount of xanthine oxidoredutase was decreased in the irradiated epithelium. It is presumed that xanthine oxidoreductase might be released extracellularly (into tears) or the enzyme molecules were denatured due to UVB rays (particulary after the longer procedure). Comparative histochemical and biochemical findings suggest that reactive oxygen species-generating oxidases (xanthine oxidase, D-amino acid oxidase) contribute to the corneal damage evoked by UVB rays.
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