Influence of an extremely low frequency magnetic field (ELF-EMF) on antioxidative vitamin E properties in AT478 murine squamous cell carcinoma culture in vitro.

International journal of toxicology · 2010 · Benefit · Low evidence

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BenefitLow evidencePaper 4388

Vitamin E treatment increased antioxidant enzyme activity in an exposure-dependent manner. ELF-EMF alone or combined with vitamin E increased superoxide dismutase and glutathione peroxidase activities compared to control. ELF-EMF alters antioxidative activiti…

Study snapshot

PublicationInternational journal of toxicology · 2010
Study typein_vitro
Reported directionBenefit
Evidence ratingLow

Abstract

This study examines the effects of vitamin E and an extremely low frequency electromagnetic field (ELF-EMF) and their combination in different time intervals of exposure of vitamin E (tocopherol) on the AT478 murine squamous cell carcinoma line. This study provides insight into the influence of correlations between ELF-EMF and vitamin E supplementation on antioxidant enzyme activity in malignant cells in vitro. Following vitamin E treatment, activity of the antioxidant enzymes is increased in an exposure-dependent manner compared with the untreated group. Application of ELF-EMF alone or with vitamin E increases both superoxide dismutase isoenzymes and glutathione peroxidase activities in comparison to the control group. The results suggest that ELF-EMF alters antioxidative activities of vitamin E in AT478 tumor cells. This study confirms the role of vitamin E in decreasing susceptibility to lipid peroxidation in AT478 tumor cells.

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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 typein_vitro
Effect directionbenefit
PopulationAT478 murine squamous cell carcinoma cell line
Sample sizeNot supplied
ExposureELF
Evidence strengthLowConfidence: 30% · Peer reviewed: yes

Main findings

Vitamin E treatment increased antioxidant enzyme activity in an exposure-dependent manner. ELF-EMF alone or combined with vitamin E increased superoxide dismutase and glutathione peroxidase activities compared to control. ELF-EMF alters antioxidative activities of vitamin E in AT478 tumor cells and vitamin E decreases susceptibility to lipid peroxidation.

Outcomes measured

  • antioxidant enzyme activity
  • superoxide dismutase isoenzymes activity
  • glutathione peroxidase activity
  • lipid peroxidation susceptibility

Limitations

  • in vitro study, limiting direct applicability to humans
  • no information on exposure frequency or intensity
  • no sample size reported
View raw extracted JSON
{
  "study_type": "in_vitro",
  "exposure": {
    "band": "ELF",
    "source": null,
    "frequency_mhz": null,
    "sar_wkg": null,
    "duration": null
  },
  "population": "AT478 murine squamous cell carcinoma cell line",
  "sample_size": null,
  "outcomes": [
    "antioxidant enzyme activity",
    "superoxide dismutase isoenzymes activity",
    "glutathione peroxidase activity",
    "lipid peroxidation susceptibility"
  ],
  "main_findings": "Vitamin E treatment increased antioxidant enzyme activity in an exposure-dependent manner. ELF-EMF alone or combined with vitamin E increased superoxide dismutase and glutathione peroxidase activities compared to control. ELF-EMF alters antioxidative activities of vitamin E in AT478 tumor cells and vitamin E decreases susceptibility to lipid peroxidation.",
  "effect_direction": "benefit",
  "limitations": [
    "in vitro study, limiting direct applicability to humans",
    "no information on exposure frequency or intensity",
    "no sample size reported"
  ],
  "evidence_strength": "low",
  "confidence": 0.3,
  "peer_reviewed_likely": "yes",
  "keywords": [
    "ELF-EMF",
    "vitamin E",
    "antioxidant enzymes",
    "murine squamous cell carcinoma",
    "in vitro",
    "oxidative stress"
  ],
  "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: 10.1177/1091581809352011
PubMed: 20335516

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