PMID- 22323476 OWN - NLM STAT- MEDLINE DCOM- 20140409 LR - 20130521 IS - 1477-0393 (Electronic) IS - 0748-2337 (Linking) VI - 29 IP - 5 DP - 2013 Jun TI - The effects of exposure to electromagnetic field on rat myocardium. PG - 418-25 LID - 10.1177/0748233711434957 [doi] AB - Exposure to electromagnetic fields (EMFs) causes increased adverse effects on biological systems. The aim of this study was to investigate the effects of EMF on heart tissue by biochemical and histomorphological evaluations in EMF-exposed adult rats. In this study, 28 male Wistar rats weighing 200-250 g were used. The rats were divided into two groups: sham group (n = 14) and EMF group (n = 14). Rats in sham group were exposed to same conditions as the EMF group except the exposure to EMF. Rats in EMF group were exposed to a 50-Hz EMF of 3 mT for 4 h/day and 7 days/week for 2 months. After 2 months of exposure, rats were killed; the hearts were excised and evaluated. Determination of oxidative stress parameters was performed spectrophotometrically. To detect apoptotic cells, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining and caspase-3 immunohistochemistry were performed. In EMF-exposed group, levels of lipid peroxidation significantly increased and activities of superoxide dismutase and glutathione peroxidase decreased compared with sham group. The number of TUNEL-positive cells and caspase-3 immunoreactivity increased in EMF-exposed rats compared with sham. Under electron microscopy, there were mitochondrial degeneration, reduction in myofibrils, dilated sarcoplasmic reticulum and perinuclear vacuolization in EMF-exposed rats. In conclusion, the results show that the exposure to EMF causes oxidative stress, apoptosis and morphologic damage in myocardium of adult rats. The results of our study indicate that EMF-related changes in rat myocardium could be the result of increased oxidative stress. Further studies are needed to demonstrate whether the exposure to EMF can induce adverse effects on myocardium. FAU - Kiray, Amac AU - Kiray A AD - Department of Anatomy, Dokuz Eylul University Medical School, Turkey. FAU - Tayefi, Hamid AU - Tayefi H FAU - Kiray, Muge AU - Kiray M FAU - Bagriyanik, Husnu Alper AU - Bagriyanik HA FAU - Pekcetin, Cetin AU - Pekcetin C FAU - Ergur, Bekir Ugur AU - Ergur BU FAU - Ozogul, Candan AU - Ozogul C LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120209 PL - England TA - Toxicol Ind Health JT - Toxicology and industrial health JID - 8602702 RN - 4Y8F71G49Q (Malondialdehyde) RN - EC 1.11.1.9 (Glutathione Peroxidase) RN - EC 1.15.1.1 (Superoxide Dismutase) SB - IM MH - Animals MH - Apoptosis/radiation effects MH - Electromagnetic Fields/*adverse effects MH - Glutathione Peroxidase/metabolism MH - Heart/*radiation effects MH - Immunohistochemistry MH - Male MH - Malondialdehyde/metabolism MH - Myocardium/enzymology/metabolism/pathology MH - Oxidative Stress/radiation effects MH - Rats MH - Rats, Wistar MH - Statistics, Nonparametric MH - Superoxide Dismutase/metabolism OTO - NOTNLM OT - Electromagnetic field OT - apoptosis OT - myocardium OT - oxidative stress OT - ultrastructure EDAT- 2012/02/11 06:00 MHDA- 2014/04/10 06:00 CRDT- 2012/02/11 06:00 PHST- 2012/02/11 06:00 [entrez] PHST- 2012/02/11 06:00 [pubmed] PHST- 2014/04/10 06:00 [medline] AID - 0748233711434957 [pii] AID - 10.1177/0748233711434957 [doi] PST - ppublish SO - Toxicol Ind Health. 2013 Jun;29(5):418-25. doi: 10.1177/0748233711434957. Epub 2012 Feb 9.