To study whether exposure to 50 Hz extremely low frequency sinusoidal electromagnetic field affects the expression and production of inducible nitric oxide synthase (iNOS) and monocyte chemotactic protein-1 (MCP-1, a chemokine) in human monocytes.
Chemokines and iNOS play a central role in various immunological and inflammatory processes. NO and MCP-1 reciprocally modulate their expression and play an important, but not fully defined role, in the development and progression of many diseases.
Cells from each subject (n=10) were divided into four groups: 1) control cells, 2) cells stimulated with LPS, 3) control cells exposed to electromagnetic fields, 4) cells stimulated with LPS and exposed to electromagnetic fields.
Exposure | Parameters |
---|---|
Exposure 1:
50 Hz
Exposure duration:
overnight
|
cells were treated in four groups: i) control ii) cells stimulated with lipopolysaccharide (LPS, 10 µg/ml) iii) cells exposed to EMF iv) cells stimulated with LPS and exposed to EMF
Frequency | 50 Hz |
---|---|
Type | |
Waveform | |
Exposure duration | overnight |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
magnetic flux density | 1 mT | effective value | measured | - | - |
The data showed that the electromagnetic field exposure affects the expression of iNOS and MCP-1 in human monocytes in vitro at the mRNA level and protein synthesis. The effects of exposure clearly differed with respect to the potentiation and inhibition of iNOS and MCP-1 expression: Whereas iNOS was down-regulated both at the mRNA level and at the protein level, MCP-1 was up-regulated.
In conclusion, electromagnetic fields may represent a non-pharmacological inhibitor of NO and an inducer of MCP-1, which activate one of theses molecules and lead to inhibition of the other or vice versa, establishing a mechanism that protects cells from excess stimulation and contributes to the regulation of cell homeostasis. These findings provide helpful information regarding the electromagnetic field-mediated modulation of the inflammatory response in vivo.
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