Author(s):
Bodin R*, Godin L, Mougin C, Lecomte A, Larrigaldie V, Feat-Vetel J et al.
* PERITOX Laboratory (UMR_I 01), UPJV/INERIS INERIS, MIV/TEAM, Verneuil-en-Halatte France University of Picardie Jules Verne, CURS, Amiens.
France
Published in:
Neurotoxicology 2025; 111: 103312
Published: 02.09.2025
on EMF:data since 09.10.2025
Further publications: Study funded by:

French Ministry of Ecology Program 190.

Medical/biological studies
Go to EMF:data assessment

Altered development in rodent brain cells after 900 MHz radiofrequency exposure.

Original Abstract

Health risks related to 900 MHz 2 G frequency exposure remain inconclusive under current regulatory standards. Research into potential long-term effects is ongoing, particularly as the use of mobile networks and wireless devices increases. This study investigates the effects of non-thermal exposure levels of mobile phone 900 MHz radiofrequency electromagnetic field (RF-EMF) on rodent neurodevelopment. In vivo, the effects of pre- and post-natal 0.08 and 0.4 W/kg specific absorption rate (SAR) exposure were assessed for their impact on the proteomic profile at postnatal day 0 (PND 0). Brain-derived neurotrophic factor (BDNF), BrdU+ proliferative cells, synaptogenesis, and oxidative stress in the hippocampus and cortex of rat pups were studied at PND 8 and PND 17. Effects of the lowest SAR (0.08 W/kg) were assessed in vitro to afford mechanistic data regarding neural stem cells (NSCs) differentiation. In vivo results showed a decrease in BDNF level and BrdU+ proliferative cells with a decrease in synapse balance (excitatory synapses/inhibitory synapses). In vitro, at 0.08 W/kg there was an increase in Ki-67 + proliferative cells, apoptosis, and double-strand DNA breaks in NSCs. A lower ratio of B1 cells (primary progenitors of NSCs) among total cerebral cells and a higher ratio of oligodendrocyte progenitor cells and astrocytes were observed in the exposed NSCs. Our findings suggest that key cellular events for brain ontogenesis are likely to undergo changes with RF-EMF 900 MHz exposure during early development. These support the hypothesis that the developing central nervous system is vulnerable to RF-EMF exposures in rodents at regulatory thresholds.

Keywords

Radiofrequency fields | Proliferation | Synaptogenesis | Neuroproteomics | Neurodevelopment |Neurotoxicology | Stem cells

Exposure:

900 MHz
SAR: 0.08; 0.4 W/kg

EMF:data assessment

Summary

The ICNIRP has established exposure guidelines for radiofrequency (RF) radiation: 0.08 W/kg for the general population and 0.4 W/kg for occupationally exposed persons. However, it is unclear whether these guidelines provide adequate protection. Previous studies have shown that exposure to comparable levels can cause oxidative stress and altered growth in rodents. These biological effects may occur at these thresholds, especially during sensitive developmental stages. Thus, this study examined the impact of 2G radiofrequency (RF) exposure on the developing brain by using in vivo and in vitro rat models. The ICNIRP limits were adhered to. Most synapses in rats form between postnatal days (PND) 0 and 21, with synaptogenesis (the formation of synapses) peaking during PND 14. In human children, this peak occurs between the ages of 1 and 2. This study focused on proteomic changes and cellular parameters, including proliferation, synaptogenesis, and differentiation of neural cells.

Source: ElektrosmogReport | Issue 4/2025

Study design and methods

The male Sprague Dawley rats were examined after being exposed in utero from the eighth day of gestation until the seventh postnatal day at most. The rats were exposed to 900 MHz radiation at either the public exposure limit (30.2 V/m; whole-body SAR 0.08 W/kg) or the occupational exposure limit (67.5 V/m; whole-body SAR 0.4 W/kg). The controls were sham-exposed. A total of 9 control animals (n = 9) and 8 exposed animals (n = 8) were exposed. Examined endpoints included proteomic analyses of the hippocampus and cortex immediately after birth; quantification of brain-derived neurotrophic factor (BDNF), which is essential for maintaining and developing neurons and synapses, as well as memory processes; cell proliferation; the number of synapses and the balance between excitatory and inhibitory synapses; and oxidative stress markers in the hippocampus and cortex on the postnatal days (PND) 8 and 17. (Due to the different time points, the number of animals available for respective endpoint analyses varied from n = 3 to n = 9; editor's note.) These in vivo studies were supplemented by in vitro analyses of neural stem cells. The cells were exposed to 900 MHz radiation and 0.08 W/kg for 3 or 7 days. The scientists evaluated cell differentiation, cell proliferation, and DNA damage.

Results

Proteomic analysis on postnatal day (PND) 0 revealed different expression levels of 10 proteins in the exposed groups compared to the sham-exposed control group. These changes primarily affected proteins associated with synapse formation and cell growth. A significant decrease in the number of synapses was observed in the hippocampus of young animals exposed on PND 8. The balance between excitatory and inhibitory synapses shifted significantly toward inhibitory synapses in both exposed groups. Both effects leveled off by PND 17. There were no significant differences in the number of synapses in the cortex. However, the balance shifted significantly in the more heavily exposed group on PND 17. In the cortex, but not the hippocampus, there were significantly fewer proliferating cells on PND 8. A significant decrease in BDNF levels was also observed on PND 17. Examination of oxidative stress markers showed no significant changes. In vitro, there were significantly more apoptotic and proliferating cells, as well as DNA double-strand breaks. In addition, there was a statistically significant change in the differentiation pattern of neural stem cells.

Conclusions

The study data suggest that exposure within regulatory limits for the general population may adversely impact brain development. These changes include reduced cell proliferation, BDNF levels, and synapse formation in vivo, as well as changes in neural stem cell differentiation in vitro. The authors hypothesize that the increase in inhibitory synapses may result from increased neuronal excitability of the organism. Changes in this balance have been linked to developmental disorders of the nervous system, such as autism spectrum disorder. In summary, the scientists' hypothesis that developing organisms are susceptible to RF radiation is confirmed. They recommend exercising caution when using mobile devices, especially around pregnant women and young children.

Editor's note:

The study design is impressive thanks to its combination of in vivo and in vitro experiments and a multimodal approach that includes proteomics, immunohistochemistry, and functional analyses. The study's significance is also enhanced by its use of low field strengths that fall within regulatory limits for the general population. However, there are areas for improvement. For example, the total number of experimental animals is small, and the number varies depending on the endpoints investigated. While the chosen study times are well-selected in terms of neural development, an additional study including adult animals would have been desirable to analyze functional consequences that may persist into adulthood. As with any animal model, the question of transferability to humans arises. Nevertheless, the data suggest that regulatory limits may not be safe at all stages of development. (RH)