Effects of wireless local area network exposure on testicular morphology and VEGF levels
← Research streamCompared with controls, rats exposed to 2.45 GHz EMF showed increased VEGFA gene expression (p < 0.05) and VEGFA protein levels (p < 0.001), with no significant change in HIF1A gene expression. Histology showed reduced seminiferous tubule diameter, epithelial…
Study snapshot
Abstract
Category: Toxicology Tags: EMF, wireless LAN, testicular damage, VEGF, HIF1A-VEGF pathway, male fertility, 2.45 GHz DOI: 10.1038/s41598-026-37323-2 URL: nature.com Overview This study investigated the impact of exposure to a 2.45 GHz electromagnetic field (EMF), typical of wireless local area networks (WLAN), on testicular health in rats. The focus was on both histological changes and alterations in the HIF1A-VEGF pathway, crucial for vascular function and tissue health. - 🌡️ Twenty-four adult male albino Wistar rats were divided into a control group (no EMF exposure) and an experimental group (exposed to 2.45 GHz microwave radiation at 3 V/m, SAR 0.00208 W/kg) for one hour daily over 60 days. - 🔬 Testicular tissue was analyzed post-exposure for: - Histopathological changes - Gene expression levels (VEGFA and HIF1A) - VEGFA protein concentration Findings - ⬆️ VEGFA gene expression (p < 0.05) and protein levels (p < 0.001) were elevated in the EMF-exposed group, while HIF1A expression remained unchanged. - 🔻 Significant histological damage was observed in the EMF group: - Reduced seminiferous tubule diameter (p < 0.001) - Decreased epithelial thickness (p < 0.001) - Lower tubule density (p < 0.001) - Reduced Sertoli cell count (p = 0.0098) Conclusion Exposure to EMF at 2.45 GHz increases VEGF levels independently of HIF1A, suggesting the risk of testicular damage associated with wireless LAN frequency EMF. This provides clear evidence of a link between EMF exposure and male reproductive health risks.
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
Compared with controls, rats exposed to 2.45 GHz EMF showed increased VEGFA gene expression (p < 0.05) and VEGFA protein levels (p < 0.001), with no significant change in HIF1A gene expression. Histology showed reduced seminiferous tubule diameter, epithelial thickness, tubule density (all p < 0.001), and Sertoli cell count (p = 0.0098) in the exposed group.
Outcomes measured
- Testicular histopathology (seminiferous tubule diameter, epithelial thickness, tubule density, Sertoli cell count)
- VEGFA gene expression
- HIF1A gene expression
- VEGFA protein concentration
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "microwave",
"source": "wireless local area network (WLAN) / 2.45 GHz EMF",
"frequency_mhz": 2450,
"sar_wkg": 0.00208,
"duration": "1 hour daily for 60 days"
},
"population": "Adult male albino Wistar rats",
"sample_size": 24,
"outcomes": [
"Testicular histopathology (seminiferous tubule diameter, epithelial thickness, tubule density, Sertoli cell count)",
"VEGFA gene expression",
"HIF1A gene expression",
"VEGFA protein concentration"
],
"main_findings": "Compared with controls, rats exposed to 2.45 GHz EMF showed increased VEGFA gene expression (p < 0.05) and VEGFA protein levels (p < 0.001), with no significant change in HIF1A gene expression. Histology showed reduced seminiferous tubule diameter, epithelial thickness, tubule density (all p < 0.001), and Sertoli cell count (p = 0.0098) in the exposed group.",
"effect_direction": "harm",
"limitations": [],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"2.45 GHz",
"microwave radiation",
"WLAN",
"Wi-Fi",
"rat",
"testis",
"testicular morphology",
"VEGFA",
"HIF1A",
"Sertoli cells",
"seminiferous tubules",
"SAR"
],
"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: 10.1038/s41598-026-37323-2
PubMed: Not supplied
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