Differential metabolic responses of mouse Leydig and spermatogonia cells to radiofrequency electromagnetic field exposure

Authors: Miao Xia, Lin Yanyun, Guo Juan, Lin Jiajin, Gao Peng, Zhang Wei, Zeng Lihua, Guo Guozhen, Li Jing

Year: 2025

Category: Reproductive Biology, Metabolomics

Journal: Frontiers in Public Health

DOI: 10.3389/fpubh.2025.1623701

URL: https://www.frontiersin.org/journals/public-health/articles/10.3389/fpubh.2025.1623701/full

Abstract

Introduction

Existing studies have shown that radiofrequency electromagnetic fields (RF-EMFs) have a variety of effects on living organisms. However, the specific impact of RF-EMFs on the metabolism of reproductive cells and the underlying mechanisms remain unclear.

This study aims to explore the effects of RF-EMFs on the metabolism of mouse Leydig cells (TM3) and spermatogonia cells (GC-1) using metabolomics analysis. The goal is to reveal potential mechanisms by which RF-EMFs affect reproductive health.

Methods

  • Used liquid chromatography-mass spectrometry (LC-MS) to analyze metabolomic profiles.
  • Examined TM3 and GC-1 cells under two irradiation modalities: continuous and intermittent RF-EMF exposure.
  • Employed KEGG pathway analysis for significantly enriched metabolic pathways.
  • Used ELISA to detect glutathione levels.

Results

  • Continuous irradiation had a more pronounced impact on TM3 cell metabolism, particularly affecting:
    • Amino acid metabolism
    • The citric acid cycle
    • ABC transporters
    • Bile secretion
    • Glutathione metabolism
  • Intermittent irradiation altered levels of fatty acyls and purine nucleosides, showing
    • Significant enrichment in purine metabolism
    • Biosynthesis of unsaturated fatty acids
    • Fatty acid metabolism
  • GC-1 cells exhibited lower sensitivity to RF-EMF irradiation compared to TM3 cells.
  • Both irradiation modalities affected purine metabolism and lysine degradation pathways in TM3 cells.
  • ADP level changes may serve as a key metabolic signature in cellular response to RF-EMF exposure.

Conclusion

Continuous RF-EMF irradiation significantly impacts TM3 cell metabolism especially in amino acid and glutathione pathways, while intermittent irradiation mainly disturbs fatty acyl and purine metabolism. GC-1 cells are less sensitive to RF-EMF. Changes in ADP levels may represent a key metabolic signature of RF-EMF exposure. These metabolic disturbances are evidence of a mechanistic link between RF-EMF exposure and altered reproductive cell function, indicating potential health risks associated with EMF exposure.

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