Alterations in antioxidant defense system of workers chronically exposed to arsenic, cadmium and mercury from coal flying ash

Humans are exposed to different stress factors that are responsible for over-production of reactive oxygen species. Exposure to heavy metals is one of these factors. The aim of the study was to analyze the effect of chronic exposure to heavy metals through coal flying ash on the efficiency of antiox...

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Published inEnvironmental geochemistry and health Vol. 38; no. 1; pp. 65 - 72
Main Authors Zeneli, Lulzim, Sekovanić, Ankica, Ajvazi, Majlinda, Kurti, Leonard, Daci, Nexhat
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.02.2016
Springer Nature B.V
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ISSN0269-4042
1573-2983
1573-2983
DOI10.1007/s10653-015-9683-2

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Summary:Humans are exposed to different stress factors that are responsible for over-production of reactive oxygen species. Exposure to heavy metals is one of these factors. The aim of the study was to analyze the effect of chronic exposure to heavy metals through coal flying ash on the efficiency of antioxidative defensive mechanisms, represented by the activity of superoxide dismutase, glutathione peroxidase and ascorbic acid. Nonessential elements such as arsenic and mercury levels showed a significant increase ( p  > 0.001) in the power plant workers rather than in the control subjects. There were no significant differences of blood cadmium between power plant workers and control subjects. We found a significant positive correlation ( p  < 0.05) between BAs/SZn ( r  = 0.211), BAs/BSe ( r  = 0.287), BCd/SCu ( r  = 0.32) and BHg/BSe ( r  = 0.263) in the plant workers. Red blood cell antioxidant enzymes and plasma ascorbic acid were significantly lower in power plants workers than in the control group ( p  < 0.002). We can conclude that levels of mercury, arsenic and cadmium in blood, despite their concentration within the reference values, significantly affect plasma ascorbic acid concentration, superoxide dismutase and glutathione peroxidase activity, which are able to increase the risk of oxidative stress.
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ISSN:0269-4042
1573-2983
1573-2983
DOI:10.1007/s10653-015-9683-2