[Effects of extremely low frequency electromagnetic fields on apoptosis and cell cycle of mouse brain and liver cells].
← Research streamMice exposed to 50 Hz electromagnetic fields at 0.2 mT or 6.0 mT for 2 weeks had higher apoptosis rates in brain and liver cells than controls, with statistically significant differences (P<0.05). Exposed mice also showed increased G0/G1 cell percentages and …
Study snapshot
Abstract
OBJECTIVE: To study the effects of extremely low frequency electromagnetic fields (ELF EMFs) on apoptosis and cell cycle of mouse brain and liver cells. METHODS: Mice were exposed to 50 Hz, 0.2 mT or 6.0 mT electromagnetic fields for 2 weeks. TUNEL and flow cytometric methods were used to analyze apoptosis and cell cycle of brain and liver cells. RESULTS: After exposure to 0.2 mT and 6.0 mT ELF EMFs for 2 weeks, apoptosis rates of brain cells [(5.60 +/- 1.47)% and (4.73 +/- 0.48)% respectively] were higher than that of control [(2.90 +/- 0.75)%], and apoptosis rates of liver cells [(4.19 +/- 2.08)% and (3.38 +/- 0.65)% respectively] were higher than that of control [(1.84 +/- 0.76)%]. G0/G1 cell percentage of brain cells [(80.21 +/- 1.68)% and (79.54 +/- 0.56)% respectively] were higher than that of control [(76.85 +/- 0.83)%], and those of liver cells [(79.42 +/- 1.80)% and (80.47 +/- 1.79)% respectively] were higher than that of control [(73.36 +/- 3.10)%]. The above differences were all statistically significant as P < 0.05. At the same time S and G2 + M cell percentage of brain and liver cells were significantly decreased. CONCLUSION: Exposure to 50 Hz EMFs may alter cell cycle and induce apoptosis of mouse brain and liver cells.
AI evidence extraction
Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.
Main findings
Mice exposed to 50 Hz electromagnetic fields at 0.2 mT or 6.0 mT for 2 weeks had higher apoptosis rates in brain and liver cells than controls, with statistically significant differences (P<0.05). Exposed mice also showed increased G0/G1 cell percentages and decreased S and G2+M percentages in brain and liver cells versus controls (P<0.05).
Outcomes measured
- Apoptosis (TUNEL; flow cytometry)
- Cell cycle distribution (G0/G1, S, G2+M; flow cytometry)
Limitations
- Sample size not reported in abstract
- Limited exposure durations assessed (2 weeks only)
- Only two field intensities tested (0.2 mT and 6.0 mT)
- Outcomes limited to apoptosis and cell-cycle measures in brain and liver cells
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": 5e-05,
"sar_wkg": null,
"duration": "2 weeks"
},
"population": "Mice (mouse brain and liver cells)",
"sample_size": null,
"outcomes": [
"Apoptosis (TUNEL; flow cytometry)",
"Cell cycle distribution (G0/G1, S, G2+M; flow cytometry)"
],
"main_findings": "Mice exposed to 50 Hz electromagnetic fields at 0.2 mT or 6.0 mT for 2 weeks had higher apoptosis rates in brain and liver cells than controls, with statistically significant differences (P<0.05). Exposed mice also showed increased G0/G1 cell percentages and decreased S and G2+M percentages in brain and liver cells versus controls (P<0.05).",
"effect_direction": "harm",
"limitations": [
"Sample size not reported in abstract",
"Limited exposure durations assessed (2 weeks only)",
"Only two field intensities tested (0.2 mT and 6.0 mT)",
"Outcomes limited to apoptosis and cell-cycle measures in brain and liver cells"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"extremely low frequency",
"ELF EMF",
"50 Hz",
"0.2 mT",
"6.0 mT",
"mouse",
"brain cells",
"liver cells",
"apoptosis",
"TUNEL",
"flow cytometry",
"cell cycle",
"G0/G1",
"S phase",
"G2/M"
],
"suggested_hubs": [
{
"slug": "occupational-exposure",
"weight": 0.35,
"reason": "Published in an industrial hygiene/occupational diseases journal and involves ELF field exposure relevant to occupational settings."
}
]
}AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.
Identifiers and source
DOI: Not supplied
PubMed: 14761394
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