Exposure to extremely low-frequency electromagnetic fields inhibits T-type calcium channels via AA/LTE4 signaling pathway.
← Research streamIn HEK293 cells transfected with human T-type calcium channels, 50 Hz ELF-EMF exposure inhibited Cav3.1, Cav3.2, and Cav3.3 channel activity. ELF-EMF (50 Hz, 0.2 mT) did not alter Cav3.2 protein expression or steady-state activation/inactivation kinetics, but…
Study snapshot
Abstract
Extremely low-frequency electromagnetic fields (ELF-EMF) causes various biological effects through altering intracellular calcium homeostasis. The role of high voltage-gated (HVA) calcium channels in ELF-EMF induced effects has been extensively studied. However, the effect of ELF-EMF on low-voltage-gated (LVA) T-type calcium channels has not been reported. In this study, we test the effect of ELF-EMF (50Hz) on human T-type calcium channels transfected in HEK293 cells. Conversely to its stimulant effects on HVA channels, ELF-EMF exposure inhibited all T-type (Cav3.1, Cav3.2 and Cav3.3) channels. Neither the protein expression nor the steady-state activation and inactivation kinetics of Cav3.2 channels were altered by ELF-EMF (50Hz, 0.2mT) exposure. Exposure to ELF-EMF increased both arachidonic acid (AA) and leukotriene E4 (LTE4) levels in HEK293 cells. CAY10502 and bestatin, which block the increase of AA and LTE4 respectively, abrogated the ELF-EMF inhibitory effect on Cav3.2 channels. Exogenous LTE4 mimicked the ELF-EMF inhibition of T-type calcium channels. ELF-EMF (50Hz) inhibits native T-type calcium channels in primary cultured mouse cortical neurons via LTE4. We conclude that 50Hz ELF-EMF inhibits T-type calcium channels through AA/LTE4 signaling pathway.
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
In HEK293 cells transfected with human T-type calcium channels, 50 Hz ELF-EMF exposure inhibited Cav3.1, Cav3.2, and Cav3.3 channel activity. ELF-EMF (50 Hz, 0.2 mT) did not alter Cav3.2 protein expression or steady-state activation/inactivation kinetics, but increased AA and LTE4 levels; blocking AA or LTE4 increases abrogated the inhibitory effect, and exogenous LTE4 mimicked it. ELF-EMF (50 Hz) also inhibited native T-type calcium channels in primary cultured mouse cortical neurons via LTE4.
Outcomes measured
- T-type (LVA) calcium channel activity (Cav3.1, Cav3.2, Cav3.3)
- Cav3.2 protein expression
- Steady-state activation/inactivation kinetics of Cav3.2
- Arachidonic acid (AA) levels
- Leukotriene E4 (LTE4) levels
- Native T-type calcium channel activity in primary cultured mouse cortical neurons
Limitations
- In vitro/cell culture and primary neuron culture models; findings may not generalize to in vivo conditions
- Exposure duration not reported in the abstract
- Sample sizes not reported in the abstract
- Mechanistic pathway inference based on pharmacologic blockers; potential off-target effects not described in the abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": 0.05,
"sar_wkg": null,
"duration": null
},
"population": null,
"sample_size": null,
"outcomes": [
"T-type (LVA) calcium channel activity (Cav3.1, Cav3.2, Cav3.3)",
"Cav3.2 protein expression",
"Steady-state activation/inactivation kinetics of Cav3.2",
"Arachidonic acid (AA) levels",
"Leukotriene E4 (LTE4) levels",
"Native T-type calcium channel activity in primary cultured mouse cortical neurons"
],
"main_findings": "In HEK293 cells transfected with human T-type calcium channels, 50 Hz ELF-EMF exposure inhibited Cav3.1, Cav3.2, and Cav3.3 channel activity. ELF-EMF (50 Hz, 0.2 mT) did not alter Cav3.2 protein expression or steady-state activation/inactivation kinetics, but increased AA and LTE4 levels; blocking AA or LTE4 increases abrogated the inhibitory effect, and exogenous LTE4 mimicked it. ELF-EMF (50 Hz) also inhibited native T-type calcium channels in primary cultured mouse cortical neurons via LTE4.",
"effect_direction": "mixed",
"limitations": [
"In vitro/cell culture and primary neuron culture models; findings may not generalize to in vivo conditions",
"Exposure duration not reported in the abstract",
"Sample sizes not reported in the abstract",
"Mechanistic pathway inference based on pharmacologic blockers; potential off-target effects not described in the abstract"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"ELF-EMF",
"50 Hz",
"0.2 mT",
"T-type calcium channels",
"Cav3.1",
"Cav3.2",
"Cav3.3",
"HEK293",
"mouse cortical neurons",
"arachidonic acid",
"leukotriene E4",
"LTE4",
"AA/LTE4 signaling pathway"
],
"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: 10.1016/j.ceca.2013.11.002
PubMed: 24360572
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