The effects of a 1.8 GHz continuous electromagnetic fields on mucociliary transport of human nasal mucosa.
← Research streamHuman nasal mucosa cells exposed to a 1.8 GHz continuous EMF (SAR=1.0 W/kg) showed decreased ciliary beat frequency compared with controls, without a detected difference in survival rates. PKC activity increased in the EMF-exposed group, and PKC inhibitors (C…
Study snapshot
Abstract
OBJECTIVES/HYPOTHESIS: The aim of this study was to investigate the effects of a 1.8 GHz continuous electromagnetic fields (EMF) on human nasal mucociliary transport, and to determine the pathophysiology of ciliary beat frequency (CBF) during an EMF-induced change. METHODS: Human nasal mucosa cells were exposed to a 1.8 GHz EMF (SAR=1.0 W/kg), and CBF was analyzed using an optical flow technique with the peak detection method. RESULTS: The 1.8 GHz-exposed group showed a decreased CBF when compared to the control group. In the cytotoxicity assay, difference in survival rates was not found between the two groups. In the EMF-exposed group, protein kinase C (PKC) activity was increased during a PKC activity assay. The broad PKC inhibitor, Calphostin C abolished the EMF-induced decrease of CBF. The EMF-induced decrease of CBF was abolished by GF 109203X, a novel PKC (nPKC) isoform inhibitor, whereas the decrease was not attenuated by Gö-6976, a specific inhibitor of conventional PKC (cPKC) isoform. CONCLUSIONS: EMF may inhibit CBF via an nPKC-dependent mechanism. Therefore, we have confirmed that EMF could decrease CBF by increasing PKC activity.
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
Human nasal mucosa cells exposed to a 1.8 GHz continuous EMF (SAR=1.0 W/kg) showed decreased ciliary beat frequency compared with controls, without a detected difference in survival rates. PKC activity increased in the EMF-exposed group, and PKC inhibitors (Calphostin C and an nPKC inhibitor GF 109203X) abolished the EMF-induced CBF decrease, while a cPKC inhibitor (Gö-6976) did not attenuate it.
Outcomes measured
- ciliary beat frequency (CBF)
- cell survival/cytotoxicity
- protein kinase C (PKC) activity
- effect of PKC inhibitors on EMF-induced CBF change
Limitations
- Exposure duration not reported in abstract
- Sample size not reported in abstract
- In vitro model; generalizability to in vivo human nasal mucosa function not established in abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "RF",
"source": null,
"frequency_mhz": 1800,
"sar_wkg": 1,
"duration": null
},
"population": null,
"sample_size": null,
"outcomes": [
"ciliary beat frequency (CBF)",
"cell survival/cytotoxicity",
"protein kinase C (PKC) activity",
"effect of PKC inhibitors on EMF-induced CBF change"
],
"main_findings": "Human nasal mucosa cells exposed to a 1.8 GHz continuous EMF (SAR=1.0 W/kg) showed decreased ciliary beat frequency compared with controls, without a detected difference in survival rates. PKC activity increased in the EMF-exposed group, and PKC inhibitors (Calphostin C and an nPKC inhibitor GF 109203X) abolished the EMF-induced CBF decrease, while a cPKC inhibitor (Gö-6976) did not attenuate it.",
"effect_direction": "harm",
"limitations": [
"Exposure duration not reported in abstract",
"Sample size not reported in abstract",
"In vitro model; generalizability to in vivo human nasal mucosa function not established in abstract"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"1.8 GHz",
"RF-EMF",
"SAR 1.0 W/kg",
"human nasal mucosa cells",
"mucociliary transport",
"ciliary beat frequency",
"PKC",
"nPKC",
"Calphostin C",
"GF 109203X",
"Gö-6976"
],
"suggested_hubs": []
}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: 10.1002/lary.23620
PubMed: 23060235
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