Effect of 900 MHz Electromagnetic Field Exposure During Different Trimesters of Pregnancy on TRPM2-Mediated Ferroptosis and Neurotoxicity in the Trigeminal Ganglion of Rats: Protective Role of Ferrostatin-1.
← Research streamPrenatal 900 MHz EMF exposure (2 h/day) during gestation was associated with reduced antioxidant capacity and increased lipid peroxidation, ROS, pro-inflammatory cytokines, apoptotic markers, and TRPM2 activation in offspring trigeminal ganglion at postnatal …
Study snapshot
Abstract
Electromagnetic field (EMF) exposure, unavoidable in modern life, is linked to oxidative stress and ferroptosis, processes linked to neurodevelopmental disorders. This study investigated the effects of EMF exposure during different pregnancy trimesters on rat offspring trigeminal ganglia (TGs), focusing on transient receptor potential melastatin 2 (TRPM2) ion channels, and assessed the neuroprotective potential of ferrostatin-1 (Fer), a ferroptosis inhibitor, against EMF-induced damage. Pregnant rats were exposed to 900 MHz EMF for 2 h/day during early (1-7 days, EMF 1), mid (8-14 days, EMF 2), or late (15-21 days, EMF 3) gestation. Fer (2.5 µmol/kg, i.p.) was administered immediately after daily EMF exposure in Fer treatment groups. Offspring TG tissues were analyzed on postnatal Day 28 using histopathological, immunohistochemical, and biochemical approaches. EMF exposure significantly reduced antioxidant capacity and elevated lipid peroxidation, reactive oxygen species (ROS), pro-inflammatory cytokines, apoptotic markers, and TRPM2 activation, with the most pronounced alterations in mid-gestation exposure. Fer administration largely normalized these parameters and reduced structural damage in TG. In conclusion, these findings suggest that prenatal EMF triggers ferroptotic/apoptotic neurodegeneration via TRPM2, and that Fer holds promise as a neuroprotective agent.
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
Prenatal 900 MHz EMF exposure (2 h/day) during gestation was associated with reduced antioxidant capacity and increased lipid peroxidation, ROS, pro-inflammatory cytokines, apoptotic markers, and TRPM2 activation in offspring trigeminal ganglion at postnatal day 28, with the most pronounced changes after mid-gestation exposure. Ferrostatin-1 administered after each daily exposure largely normalized measured parameters and reduced structural damage.
Outcomes measured
- Antioxidant capacity
- Lipid peroxidation
- Reactive oxygen species (ROS)
- Pro-inflammatory cytokines
- Apoptotic markers
- TRPM2 activation
- Histopathological/structural damage in trigeminal ganglion
- Ferroptosis-related changes (via ferrostatin-1 intervention)
Limitations
- Sample size not reported in abstract
- Specific exposure dosimetry (e.g., SAR, field strength) not reported in abstract
- Animal model; relevance to humans not established in abstract
- Outcomes assessed at a single postnatal time point (day 28)
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "RF",
"source": null,
"frequency_mhz": 900,
"sar_wkg": null,
"duration": "2 h/day during gestation (early 1–7 days, mid 8–14 days, or late 15–21 days)"
},
"population": "Pregnant rats and offspring (trigeminal ganglion assessed at postnatal day 28)",
"sample_size": null,
"outcomes": [
"Antioxidant capacity",
"Lipid peroxidation",
"Reactive oxygen species (ROS)",
"Pro-inflammatory cytokines",
"Apoptotic markers",
"TRPM2 activation",
"Histopathological/structural damage in trigeminal ganglion",
"Ferroptosis-related changes (via ferrostatin-1 intervention)"
],
"main_findings": "Prenatal 900 MHz EMF exposure (2 h/day) during gestation was associated with reduced antioxidant capacity and increased lipid peroxidation, ROS, pro-inflammatory cytokines, apoptotic markers, and TRPM2 activation in offspring trigeminal ganglion at postnatal day 28, with the most pronounced changes after mid-gestation exposure. Ferrostatin-1 administered after each daily exposure largely normalized measured parameters and reduced structural damage.",
"effect_direction": "harm",
"limitations": [
"Sample size not reported in abstract",
"Specific exposure dosimetry (e.g., SAR, field strength) not reported in abstract",
"Animal model; relevance to humans not established in abstract",
"Outcomes assessed at a single postnatal time point (day 28)"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"900 MHz",
"RF-EMF",
"pregnancy",
"trimester timing",
"rat",
"trigeminal ganglion",
"TRPM2",
"ferroptosis",
"ferrostatin-1",
"oxidative stress",
"neurotoxicity",
"apoptosis",
"inflammation"
],
"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/dneu.23013
PubMed: 41146578
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