Behavioral changes and gene profile alterations after chronic 1,950-MHz radiofrequency exposure: An observation in C57BL/6 mice

2020 · Mixed · Low evidence

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MixedLow evidencePaper 1371

In 20-month-old mice (RF-20M), open-field testing showed decreased time spent in the center and memory performance was decreased on the Y-maze and novel object recognition tests versus sham; no significant behavioral changes were reported in the 10-month-old …

Study snapshot

Publicationmanual · 2020
Study typeanimal
Reported directionMixed
Evidence ratingLow

Abstract

Behavioral changes and gene profile alterations after chronic 1,950-MHz radiofrequency exposure: An observation in C57BL/6 mice Ye Ji Jeong, Yeonghoon Son, Hyung-Do Choi, Nam Kim, Yun-Sil Lee, Young-Gyu Ko, Hae-June Lee. Behavioral changes and gene profile alterations after chronic 1,950-MHz radiofrequency exposure: An observation in C57BL/6 mice. Brain Behav. 2020 Aug 28;e01815. doi: 10.1002/brb3.1815. Abstract Introduction: Due to public concerns about deleterious biological consequences of radiofrequency electromagnetic fields (RF-EMF), the potential effects of RF-EMF on the central nervous system have received wide consideration. Methods: Here, two groups of C57BL/6 mice, aged 2 and 12 months, were exposed to 1,950-MHz RF-EMF at a specific absorption rate of 5.0 W/kg for chronic periods (2 hr/day and 5 days/week for 8 months). Behavioral changes were then assessed in the mice at 10 months (sham- or RF-10M) and 20 months (sham- or RF-20M), on the open-field test, the Y-maze test, and an object recognition memory task, while biological effects were analyzed via microarray gene profiling of the hippocampus. Results: Open-field test results showed a decrease in the time duration spent at the center while there was a decrease in enhanced memory shown by the Y-maze test and the novel object recognition test in the RF-20M mice, compared to sham-exposed mice, but no significant changes in the RF-10M group. Based on a 2-fold change cutoff, the microarray data revealed that 15 genes, which are listed as being involved in neurogenesis on Gene Ontology, were altered in both groups. Quantitative real-time PCR for validation showed increased expression of Epha8 and Wnt6 in the hippocampi of RF-20M group mice, although 13 additional genes showed no significant changes following RF-EMF exposure. Conclusion: Therefore, cognitive enhancement following chronic exposure for 8 months to RF-EMF from middle age may be associated with increases in neurogenesis-related signals in the hippocampus of C57BL/6 mice. Open access paper: onlinelibrary.wiley.com

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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.

Study typeanimal
Effect directionmixed
PopulationC57BL/6 mice (aged 2 and 12 months at start; assessed at 10 and 20 months)
Sample sizeNot supplied
ExposureRF · 1950 MHz · 5 W/kg · 2 hr/day, 5 days/week for 8 months
Evidence strengthLowConfidence: 74% · Peer reviewed: yes

Main findings

In 20-month-old mice (RF-20M), open-field testing showed decreased time spent in the center and memory performance was decreased on the Y-maze and novel object recognition tests versus sham; no significant behavioral changes were reported in the 10-month-old group (RF-10M). Microarray analysis (2-fold cutoff) identified 15 neurogenesis-related genes altered in both groups; qRT-PCR validation showed increased Epha8 and Wnt6 expression in RF-20M hippocampi, while 13 other genes were not significantly changed.

Outcomes measured

  • Behavior (open-field test)
  • Memory/cognition (Y-maze test)
  • Object recognition memory
  • Hippocampal gene expression (microarray)
  • Hippocampal gene expression validation (qRT-PCR; Epha8, Wnt6 and others)

Limitations

  • Sample size not reported in the abstract
  • Exposure source/setup not specified in the abstract
  • Behavioral results differed by age group (effects present in RF-20M but not RF-10M)
  • Most microarray-identified genes were not confirmed as significantly changed by qRT-PCR (13/15 not significant)
View raw extracted JSON
{
  "study_type": "animal",
  "exposure": {
    "band": "RF",
    "source": null,
    "frequency_mhz": 1950,
    "sar_wkg": 5,
    "duration": "2 hr/day, 5 days/week for 8 months"
  },
  "population": "C57BL/6 mice (aged 2 and 12 months at start; assessed at 10 and 20 months)",
  "sample_size": null,
  "outcomes": [
    "Behavior (open-field test)",
    "Memory/cognition (Y-maze test)",
    "Object recognition memory",
    "Hippocampal gene expression (microarray)",
    "Hippocampal gene expression validation (qRT-PCR; Epha8, Wnt6 and others)"
  ],
  "main_findings": "In 20-month-old mice (RF-20M), open-field testing showed decreased time spent in the center and memory performance was decreased on the Y-maze and novel object recognition tests versus sham; no significant behavioral changes were reported in the 10-month-old group (RF-10M). Microarray analysis (2-fold cutoff) identified 15 neurogenesis-related genes altered in both groups; qRT-PCR validation showed increased Epha8 and Wnt6 expression in RF-20M hippocampi, while 13 other genes were not significantly changed.",
  "effect_direction": "mixed",
  "limitations": [
    "Sample size not reported in the abstract",
    "Exposure source/setup not specified in the abstract",
    "Behavioral results differed by age group (effects present in RF-20M but not RF-10M)",
    "Most microarray-identified genes were not confirmed as significantly changed by qRT-PCR (13/15 not significant)"
  ],
  "evidence_strength": "low",
  "confidence": 0.74,
  "peer_reviewed_likely": "yes",
  "keywords": [
    "radiofrequency",
    "RF-EMF",
    "1950 MHz",
    "specific absorption rate",
    "SAR 5.0 W/kg",
    "chronic exposure",
    "C57BL/6 mice",
    "open-field test",
    "Y-maze",
    "novel object recognition",
    "hippocampus",
    "microarray",
    "gene profiling",
    "neurogenesis",
    "Epha8",
    "Wnt6"
  ],
  "suggested_hubs": []
}
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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/brb3.1815
PubMed: Not supplied

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