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Reproductive Health

Interactive developmental toxicity of radiofrequency radiation and 2-methoxyethanol in rats.

No Effects Found

Nelson BK, Conover DL, Shaw PB, Werren DM, Edwards RM, Hoberman AM · 1994

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Radiofrequency radiation can amplify chemical toxicity during pregnancy, causing enhanced birth defects at intermediate exposure levels.

Plain English Summary

Summary written for general audiences

Researchers exposed pregnant rats to radiofrequency radiation (10 MHz) combined with an industrial solvent called 2-methoxyethanol to see if the combination caused more birth defects than either exposure alone. They found that when combined, these exposures produced enhanced developmental damage to limbs and digits in rat fetuses, particularly when exposure occurred on day 13 of pregnancy. This suggests that EMF radiation can amplify the harmful effects of certain chemical exposures during pregnancy.

Exposure Information

A logarithmic frequency spectrum from 10 Hz to 100 GHz showing where this study's 10 MHz exposure sits relative to common EMF sources.Where This Frequency Sits on the EMF SpectrumELFVLFLF / MFHF / VHFUHFSHFmm10 Hz100 GHzThis study: 10 MHzPower lines50/60 HzCell phones~1 GHzWiFi2.4 GHz5G mm28 GHzLogarithmic scale

The study examined exposure from: 10 MHz

Study Details

We previously demonstrated that combined exposure to radiofrequency (RF; 10 MHz) radiation, which also induces hyperthermia and is teratogenic to exposed animals, and the industrial solvent, 2-methoxyethanol (2ME), produces enhanced teratogenicity in rats. The present study replicates and extends the previous research investigating the enhanced teratogenicity of combined RF radiation and 2ME exposures.

The interactive dose-related teratogenicity of RF radiation (sham exposure or maintaining colonic te...

The results are consistent with and extend our previous research findings. Synergism was observed be...

Statistical analyses did not show a global synergistic effect, but did show evidence for a synergistic effect at intermediate levels of the dose ranges. Future research will address potential interactions at lower doses.

Cite This Study
Nelson BK, Conover DL, Shaw PB, Werren DM, Edwards RM, Hoberman AM (1994). Interactive developmental toxicity of radiofrequency radiation and 2-methoxyethanol in rats. Teratology 50(4):275-293, 1994.
Show BibTeX
@article{bk_1994_interactive_developmental_toxicity_of_3270,
  author = {Nelson BK and Conover DL and Shaw PB and Werren DM and Edwards RM and Hoberman AM},
  title = {Interactive developmental toxicity of radiofrequency radiation and 2-methoxyethanol in rats.},
  year = {1994},
  
  url = {https://pubmed.ncbi.nlm.nih.gov/7716735/},
}
PubMed: 7716735

Cited By (19 papers)

View all 19 citing papers on Semantic Scholar

Quick Questions About This Study

Yes, a 1994 study found that 10 MHz radiofrequency radiation enhanced birth defects caused by the industrial solvent 2-methoxyethanol in pregnant rats. The combination produced more severe limb and digit damage than either exposure alone, particularly when exposure occurred on day 13 of pregnancy.
Research shows that 2-methoxyethanol (an industrial solvent) combined with 10 MHz radiofrequency radiation creates synergistic effects during pregnancy. The combination caused enhanced developmental damage to rat fetuses, suggesting RF radiation can amplify the harmful effects of certain chemical exposures during critical pregnancy periods.
Day 13 of pregnancy appears most vulnerable to combined RF radiation and chemical exposure. A rat study found that exposures on gestational day 13 resulted in highly significant developmental effects, while day 9 exposures showed little effect from either treatment alone or in combination.
Combined 10 MHz RF radiation and 2-methoxyethanol exposure primarily affects developing limbs and digits. The study found strong evidence of damage to forepaw digits, hindpaw digits, phalanges, metacarpals, metatarsals, and hind limbs when exposure occurred during critical pregnancy periods.
The 1994 study found synergistic effects at intermediate dose levels but didn't test the lowest possible doses. Researchers concluded that future studies should examine potential interactions at lower doses to determine the minimum levels that might cause enhanced developmental damage.