Phenotypic and genotypic characterization of antioxidant enzyme system in human population exposed to radiation from mobile towers

In the present era, cellular phones have changed the life style of human beings completely and have become an essential part of their lives. The number of cell phones and cell towers are increasing in spite of their disadvantages. These cell towers transmit radiation continuously without any interru...

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Published inMolecular and cellular biochemistry Vol. 440; no. 1-2; pp. 1 - 9
Main Authors Gulati, Sachin, Yadav, Anita, Kumar, Neeraj, Priya, Kanu, Aggarwal, Neeraj K., Gupta, Ranjan
Format Journal Article
LanguageEnglish
Published New York Springer US 01.03.2018
Springer
Springer Nature B.V
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Summary:In the present era, cellular phones have changed the life style of human beings completely and have become an essential part of their lives. The number of cell phones and cell towers are increasing in spite of their disadvantages. These cell towers transmit radiation continuously without any interruption, so people living within 100s of meters from the tower receive 10,000 to 10,000,000 times stronger signal than required for mobile communication. In the present study, we have examined superoxide dismutase (SOD) enzyme activity, catalase (CAT) enzyme activity, lipid peroxidation assay, and effect of functional polymorphism of SOD and CAT antioxidant genes against mobile tower-induced oxidative stress in human population. From our results, we have found a significantly lower mean value of manganese superoxide dismutase (MnSOD) enzyme activity, catalase (CAT) enzyme activity, and a high value of lipid peroxidation assay in exposed as compared to control subjects. Polymorphisms in antioxidant MnSOD and CAT genes significantly contributed to its phenotype. In the current study, a significant association of genetic polymorphism of antioxidant genes with genetic damage has been observed in human population exposed to radiations emitted from mobile towers.
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ISSN:0300-8177
1573-4919
DOI:10.1007/s11010-017-3150-6