Effect of puerarin on matrix metalloproteinase-2 in human fetal scleral fibroblasts treated with low frequency electromagnetic fields.
← Research streamCultured HFSFs exposed to 0.2 mT ELF-EMF for 24 h showed increased MMP-2 mRNA (0.793-fold) and protein (1.130-fold) expression. Puerarin treatment (0.1–10 microM) reversed the ELF-EMF-associated increases, with greater reversal at higher concentrations (repor…
Study snapshot
Abstract
OBJECTIVE: To study the effect of puerarin on matrix metalloproteinase-2 (MMP-2) gene and protein expression in human fetal scleral fibroblasts (HFSFs) exposed to extremely low frequency electromagnetic fields (ELF-EMF). METHODS: Cultured HFSFs were exposed to 0.2 mT ELF-EMF for 24 h. The experimental groups were divided into subgroups treated with 0, 0.1, 1 and 10 microM puerarin respectively. The expression of MMP-2 mRNA and protein were detected with real-time polymerase chain reaction and western-blot analysis respectively. RESULTS: MMP-2 mRNA and protein expression increased by 0.793 and 1.130 folds respectively under the exposure of ELF-EMFs at 0.2 mT flux density for 24 h. Puerarin at the concentration of 0.1 microM reversed this effect by 8.53% in mRNA and by 17.97% in protein expression (P < 0.05). The effect was more prominent at higher concentrations (1 and 10 microM, P < 0.01). CONCLUSION: Exposure to ELF-EMFs increased the expression of MMP-2 mRNA and protein in HFSF cells. Puerarin reversed the action to some extent in a specific concentration range. Our results implied that the puerarin might protect scleral tissue from increased expression induced by exposure to ELF-EMFs.
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
Cultured HFSFs exposed to 0.2 mT ELF-EMF for 24 h showed increased MMP-2 mRNA (0.793-fold) and protein (1.130-fold) expression. Puerarin treatment (0.1–10 microM) reversed the ELF-EMF-associated increases, with greater reversal at higher concentrations (reported as statistically significant).
Outcomes measured
- MMP-2 mRNA expression
- MMP-2 protein expression
Limitations
- In vitro cell culture model; findings may not translate to humans or tissues in vivo
- Frequency of the ELF-EMF exposure not reported in the abstract
- Sample size and replication details not reported in the abstract
- Only one field intensity (0.2 mT) and one exposure duration (24 h) reported
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": null,
"sar_wkg": null,
"duration": "24 h"
},
"population": "Human fetal scleral fibroblasts (HFSFs) in culture",
"sample_size": null,
"outcomes": [
"MMP-2 mRNA expression",
"MMP-2 protein expression"
],
"main_findings": "Cultured HFSFs exposed to 0.2 mT ELF-EMF for 24 h showed increased MMP-2 mRNA (0.793-fold) and protein (1.130-fold) expression. Puerarin treatment (0.1–10 microM) reversed the ELF-EMF-associated increases, with greater reversal at higher concentrations (reported as statistically significant).",
"effect_direction": "harm",
"limitations": [
"In vitro cell culture model; findings may not translate to humans or tissues in vivo",
"Frequency of the ELF-EMF exposure not reported in the abstract",
"Sample size and replication details not reported in the abstract",
"Only one field intensity (0.2 mT) and one exposure duration (24 h) reported"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"extremely low frequency electromagnetic fields",
"ELF-EMF",
"0.2 mT",
"human fetal scleral fibroblasts",
"HFSFs",
"matrix metalloproteinase-2",
"MMP-2",
"puerarin",
"gene expression",
"protein expression",
"RT-PCR",
"western blot"
],
"suggested_hubs": []
}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: 10.1016/s0254-6272(14)60039-x
PubMed: 24660593
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