Effect of 60 Hz electromagnetic fields on the activity of hsp70 promoter: an in vivo study.
← Research streamMice exposed to 60 Hz sinusoidal EMFs at 80 μT for 2 h daily for 7 days showed increased luciferase expression compared with controls (P<0.05), using a plasmid construct containing EMF-responsive hsp70 induction sequences and a luciferase reporter.
Study snapshot
Abstract
Exposure to EMFs (electromagnetic fields) results in a number of important biological changes, including modification of genetic expression. We have investigated the effect of 60 Hz sinusoidal EMFs at a magnetic flux density of 80 μT on the expression of the luciferase gene contained in a plasmid labelled as pEMF (EMF plasmid). This gene construct contains the specific sequences for the induction of hsp70 (heat-shock protein 70) expression by EMFs, as well as the reporter for the luciferase gene. The pEMF vector was electrotransferred into quadriceps muscles of BALB/c mice that were later exposed to EMFs. Increased luciferase expression was observed in mice exposed to EMFs 2 h daily for 7 days compared with controls (P<0.05). These data along with other reports in the literature suggest that EMFs can have far-reaching effects on the genome.
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 60 Hz sinusoidal EMFs at 80 μT for 2 h daily for 7 days showed increased luciferase expression compared with controls (P<0.05), using a plasmid construct containing EMF-responsive hsp70 induction sequences and a luciferase reporter.
Outcomes measured
- Luciferase gene expression (reporter for hsp70 promoter activity)
Limitations
- Sample size not reported in the abstract
- Outcome is a reporter gene (luciferase) in an electrotransferred plasmid construct rather than endogenous gene expression
- Exposure details beyond frequency and magnetic flux density (e.g., electric field, exposure setup) not provided in the abstract
- Findings limited to a specific in vivo muscle model in mice; generalizability to other tissues/species not addressed in the abstract
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": 0.06,
"sar_wkg": null,
"duration": "2 h daily for 7 days"
},
"population": "BALB/c mice (quadriceps muscle; in vivo plasmid electrotransfer model)",
"sample_size": null,
"outcomes": [
"Luciferase gene expression (reporter for hsp70 promoter activity)"
],
"main_findings": "Mice exposed to 60 Hz sinusoidal EMFs at 80 μT for 2 h daily for 7 days showed increased luciferase expression compared with controls (P<0.05), using a plasmid construct containing EMF-responsive hsp70 induction sequences and a luciferase reporter.",
"effect_direction": "mixed",
"limitations": [
"Sample size not reported in the abstract",
"Outcome is a reporter gene (luciferase) in an electrotransferred plasmid construct rather than endogenous gene expression",
"Exposure details beyond frequency and magnetic flux density (e.g., electric field, exposure setup) not provided in the abstract",
"Findings limited to a specific in vivo muscle model in mice; generalizability to other tissues/species not addressed in the abstract"
],
"evidence_strength": "low",
"confidence": 0.74,
"peer_reviewed_likely": "yes",
"keywords": [
"ELF-EMF",
"60 Hz",
"80 μT",
"hsp70 promoter",
"heat-shock protein 70",
"luciferase reporter",
"gene expression",
"BALB/c mice",
"in vivo",
"quadriceps muscle",
"electrotransfer",
"plasmid pEMF"
],
"suggested_hubs": [
{
"slug": "occupational-exposure",
"weight": 0.2,
"reason": "Study involves 60 Hz ELF magnetic field exposure, which can be relevant to occupational ELF contexts, though the source is not specified."
}
]
}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: 10.1042/cbr20110010
PubMed: 23124775
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