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Medical/biological Study (experimental study)Chromosomal damage in human diploid fibroblasts by intermittent exposure to extremely low-frequency electromagnetic fields. med./biol. By: Winker R, Ivancsits S, Pilger A, Adlkofer F, Rudiger HW Published in: Mutat Res 2005; 585 (1-2): 43 - 49 ( PubMed Entry , Journal web site )Aim of study (according to author) To study the effect of intermittent extremely low frequency electromagnetic fields on the induction of micronuclei and chromosome aberrations in cultured human fibroblasts.
Endpoint Exposure General category: 50/60 Hz (AC) FIELD View further expo parametersExposed system: intact cell/cell culture (in vitro) ES-1 (human diploid fibroblasts) Methods Endpoint/Measurement parameters/Methodology investigated material: DNA/RNA (in vitro), intact cell/cell culture (in vitro), chromosomes
time of investigation: after exposure
Main outcome of study (according to author) Exposure to extremely low frequency electromagnetic fields resulted in a time-dependent increase of micronuclei, which became significant after 10 h at a magnetic flux density of 1 mT. After approximately 15 h a constant level of micronuclei of about three times the basal level was reached. Additionally, chromosome aberrations were increased up to 10-fold above basal levels.
The findings strongly indicate a clastogenic potential of intermittent low frequency electromagnetic fields, which may lead to considerable chromosomal damage in dividing cells. (Study character: medical/biological study, experimental study, full/main study)
Study funded by - European Union (EU)/European Commission
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Glossary: 50/60 Hz, AC, acentric fragments, assay, biological, cell culture, cells, chromosomal, chromosome aberrations, chromosome breaks, chromosomes, clastogenic, dicentric chromosomes, diploid, DNA, electromagnetic fields, endpoint, exposure, extremely low frequency, fibroblasts, full/main study, genotoxicity, Giemsa staining, human, induction, intermittent, in vitro, lead, low frequency, magnetic flux density, micronuclei, mutation, potential, ring chromosomes, RNA, significant |
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