Evaluation of oxidative stress markers in pathogenesis of primary open-angle glaucoma

Primary open-angle glaucoma (POAG) is the leading cause of blindness in the industrial countries. It is reported that oxidative stress might be an important risk factor in the pathogenesis of POAG. Forty subjects including 20 patients with open-angle glaucoma (9 men and 12 women, mean age 61.8±12.1y...

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Veröffentlicht in:Experimental and molecular pathology 2011-04, Vol.90 (2), p.231-237
Hauptverfasser: Majsterek, Ireneusz, Malinowska, Katarzyna, Stanczyk, Malgorzata, Kowalski, Michal, Blaszczyk, Jan, Kurowska, Anna K., Kaminska, Anna, Szaflik, Jerzy, Szaflik, Jacek P.
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container_end_page 237
container_issue 2
container_start_page 231
container_title Experimental and molecular pathology
container_volume 90
creator Majsterek, Ireneusz
Malinowska, Katarzyna
Stanczyk, Malgorzata
Kowalski, Michal
Blaszczyk, Jan
Kurowska, Anna K.
Kaminska, Anna
Szaflik, Jerzy
Szaflik, Jacek P.
description Primary open-angle glaucoma (POAG) is the leading cause of blindness in the industrial countries. It is reported that oxidative stress might be an important risk factor in the pathogenesis of POAG. Forty subjects including 20 patients with open-angle glaucoma (9 men and 12 women, mean age 61.8±12.1yr) and 20 controls without glaucoma symptoms (9 men and 12 women, mean age 58.1±17.7yr) were enrolled in our study. The main aim of the work was to evaluate oxidative stress markers in the pathogenesis of open-angle glaucoma. In our work the activity of antioxidant enzymes: catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPX) as well as the total antioxidant status (TAS) was estimated. An alkaline comet assay was used to measure DNA damage of strand breaks (SB), oxidized purines as glicosylo-formamido-glicosylase (Fpg) sites, and oxidized pirmidines as endonuclease III (Nth) sites. We measured endogenous as well as exogenous DNA damage after 10μM hydrogen peroxide treatment (H2O2). We did not observe any statistical changes of DNA strand break lesion in examined POAG patients according to healthy subjects (P>0.05). However, either endogenous (P
doi_str_mv 10.1016/j.yexmp.2011.01.001
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It is reported that oxidative stress might be an important risk factor in the pathogenesis of POAG. Forty subjects including 20 patients with open-angle glaucoma (9 men and 12 women, mean age 61.8±12.1yr) and 20 controls without glaucoma symptoms (9 men and 12 women, mean age 58.1±17.7yr) were enrolled in our study. The main aim of the work was to evaluate oxidative stress markers in the pathogenesis of open-angle glaucoma. In our work the activity of antioxidant enzymes: catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPX) as well as the total antioxidant status (TAS) was estimated. An alkaline comet assay was used to measure DNA damage of strand breaks (SB), oxidized purines as glicosylo-formamido-glicosylase (Fpg) sites, and oxidized pirmidines as endonuclease III (Nth) sites. We measured endogenous as well as exogenous DNA damage after 10μM hydrogen peroxide treatment (H2O2). We did not observe any statistical changes of DNA strand break lesion in examined POAG patients according to healthy subjects (P&gt;0.05). However, either endogenous (P&lt;0.01) or exogenous (P&lt;0.001) levels of oxidative DNA damage in POAG patients were found to be statistically higher than controls. A significant decrease of antioxidant enzymes: CAT (P&lt;0.001), SOD (P&lt;0.05), and GPX (P&lt;0.001) and a non-statistical decrease of TAS status (P&gt;0.05) in glaucoma patients according to controls were also indicated. In conclusion our data revealed that oxidative stress had a pathogenic role in primary open-angle glaucoma. 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It is reported that oxidative stress might be an important risk factor in the pathogenesis of POAG. Forty subjects including 20 patients with open-angle glaucoma (9 men and 12 women, mean age 61.8±12.1yr) and 20 controls without glaucoma symptoms (9 men and 12 women, mean age 58.1±17.7yr) were enrolled in our study. The main aim of the work was to evaluate oxidative stress markers in the pathogenesis of open-angle glaucoma. In our work the activity of antioxidant enzymes: catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPX) as well as the total antioxidant status (TAS) was estimated. An alkaline comet assay was used to measure DNA damage of strand breaks (SB), oxidized purines as glicosylo-formamido-glicosylase (Fpg) sites, and oxidized pirmidines as endonuclease III (Nth) sites. We measured endogenous as well as exogenous DNA damage after 10μM hydrogen peroxide treatment (H2O2). We did not observe any statistical changes of DNA strand break lesion in examined POAG patients according to healthy subjects (P&gt;0.05). However, either endogenous (P&lt;0.01) or exogenous (P&lt;0.001) levels of oxidative DNA damage in POAG patients were found to be statistically higher than controls. A significant decrease of antioxidant enzymes: CAT (P&lt;0.001), SOD (P&lt;0.05), and GPX (P&lt;0.001) and a non-statistical decrease of TAS status (P&gt;0.05) in glaucoma patients according to controls were also indicated. In conclusion our data revealed that oxidative stress had a pathogenic role in primary open-angle glaucoma. 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We did not observe any statistical changes of DNA strand break lesion in examined POAG patients according to healthy subjects (P&gt;0.05). However, either endogenous (P&lt;0.01) or exogenous (P&lt;0.001) levels of oxidative DNA damage in POAG patients were found to be statistically higher than controls. A significant decrease of antioxidant enzymes: CAT (P&lt;0.001), SOD (P&lt;0.05), and GPX (P&lt;0.001) and a non-statistical decrease of TAS status (P&gt;0.05) in glaucoma patients according to controls were also indicated. In conclusion our data revealed that oxidative stress had a pathogenic role in primary open-angle glaucoma. Therefore, we suggested that the modulation of a pro-oxidant/antioxidant status might be a relevant target for glaucoma prevention and therapy.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>21241689</pmid><doi>10.1016/j.yexmp.2011.01.001</doi><tpages>7</tpages></addata></record>
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subjects Anti-oxidant enzyme
Antioxidants - metabolism
Biological and medical sciences
Biomarkers - metabolism
Case-Control Studies
Catalase - metabolism
Comet assay
DNA Damage
Female
Glaucoma
Glaucoma and intraocular pressure
Glaucoma, Open-Angle - enzymology
Glaucoma, Open-Angle - etiology
Glaucoma, Open-Angle - metabolism
Glutathione Peroxidase - metabolism
Humans
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Middle Aged
Ophthalmology
Oxidative DNA damage
Oxidative Stress
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Superoxide Dismutase - metabolism
title Evaluation of oxidative stress markers in pathogenesis of primary open-angle glaucoma
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