[Modulation of Ca(2+)-dependent proteinase activity in invertebrates and fish under the action of weak low-frequency magnetic fields].
← Research streamIn in vivo experiments, exposure to a weak low-frequency magnetic field tuned to the parametric resonance for Ca2+ ions was associated with a significant decrease in calpain activity in the examined animals. In in vitro experiments, preparations of Ca(2+)-dep…
Study snapshot
Abstract
The effect of weak low-frequency magnetic field on intracellular Ca(2+)-dependent proteinases (calpains) of fish and invertebrates was studied in in vivo and in vitro experiments. It has been found that intravital effect of weak low-frequency magnetic field tuned to the parametric resonance for Ca2+ ions led to a significant decrease in calpain activity in examined animals. It was shown that preparations of Ca(2+)-dependent proteinases from invertebrates and fish have been also substantially inactivated at the effect of indicated factor. Observed phenomenon is in the correspondence with an interference model of the impact of weak low-frequency magnetic field on the biological objects.
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.
Main findings
In in vivo experiments, exposure to a weak low-frequency magnetic field tuned to the parametric resonance for Ca2+ ions was associated with a significant decrease in calpain activity in the examined animals. In in vitro experiments, preparations of Ca(2+)-dependent proteinases from invertebrates and fish were also substantially inactivated under the same factor.
Outcomes measured
- Intracellular Ca(2+)-dependent proteinase (calpain) activity
Limitations
- No quantitative exposure parameters (e.g., frequency, field strength, duration) reported in the abstract.
- No sample size or species details provided.
- Outcome reporting is qualitative; effect sizes and statistical details are not described.
- Unclear experimental design details (controls, blinding, replication) from abstract alone.
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": null,
"sar_wkg": null,
"duration": null
},
"population": "Fish and invertebrates",
"sample_size": null,
"outcomes": [
"Intracellular Ca(2+)-dependent proteinase (calpain) activity"
],
"main_findings": "In in vivo experiments, exposure to a weak low-frequency magnetic field tuned to the parametric resonance for Ca2+ ions was associated with a significant decrease in calpain activity in the examined animals. In in vitro experiments, preparations of Ca(2+)-dependent proteinases from invertebrates and fish were also substantially inactivated under the same factor.",
"effect_direction": "mixed",
"limitations": [
"No quantitative exposure parameters (e.g., frequency, field strength, duration) reported in the abstract.",
"No sample size or species details provided.",
"Outcome reporting is qualitative; effect sizes and statistical details are not described.",
"Unclear experimental design details (controls, blinding, replication) from abstract alone."
],
"evidence_strength": "low",
"confidence": 0.74,
"peer_reviewed_likely": "yes",
"keywords": [
"low-frequency magnetic field",
"weak magnetic field",
"ELF",
"parametric resonance",
"Ca2+ ions",
"calpain",
"Ca(2+)-dependent proteinases",
"invertebrates",
"fish",
"in vivo",
"in vitro"
],
"suggested_hubs": [
{
"slug": "elf-magnetic-fields",
"weight": 0.9,
"reason": "Study examines biological effects of weak low-frequency (ELF) magnetic fields."
},
{
"slug": "mechanisms-calcium-signaling",
"weight": 0.75,
"reason": "Exposure is tuned to Ca2+ parametric resonance and outcome is Ca2+-dependent protease activity."
}
]
}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: 10.1134/s1068162013040080
PubMed: 24707722
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