To study the effect of acute (1h) exposure of boar spermatozoa to a 50 Hz extremely low frequency electromagnetic field on early fertility outcome.
Firstly, in vitro experiments were carried out to define the dosimetric morpho-functional influence of an acute (1 h) exposure to extremely low frequency electromagnetic field on boar spermatozoa with intensities ranging from 0 to 2 mT (at 0.25 mT of interval). Then, using the intensities identified under these in vitro conditions (minimum vs. maximum vs. median toxic dose [TD50]), in vivo experiments were performed by exposing the oviduct with (protocol A) or without spermatozoa (protocol B: capacitated spermatozoa were inserted at the end of field exposure) to extremely low frequency electromagnetic field and by evaluating the outcome of fertilization (12 h later) and the success of the early stage of embryo development (6 days later).
No exact numbers of exposed animals/oviducts or of investigated embryos are stated in the article.
Exposure | Parameters |
---|---|
Exposure 1:
50 Hz
Exposure duration:
continuous 1 h
|
|
Exposure 2:
50 Hz
Exposure duration:
continuous 1 h
|
|
Frequency | 50 Hz |
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Type | |
Waveform | |
Exposure duration | continuous 1 h |
Additional info | in vitro |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
magnetic flux density | 0 mT | minimum | - | - | raised in steps of 0.25 mT |
magnetic flux density | 2 mT | maximum | - | - | - |
Exposure source |
|
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Setup | 11 cm long PVC plane, 4 cm wide and 1 cm thick was surrounded by 144 copper wire spires (0.5 mm diameter); one oviduct inserted into the coil |
Sham exposure | A sham exposure was conducted. |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
magnetic flux density | 0 mT | minimum | - | - | raised in steps of 0.25 mT |
magnetic flux density | 2 mT | maximum | - | - | - |
The data showed that in vitro extremely low frequency electromagnetic field (> 0.5 mT) induced a progressive acrosome damage, thus compromising the ability of spermatozoa to undergo acrosomal reaction after zona pellucida stimulation and reducing the in vitro fertilization outcome. These effects became evident at 0.75 mT (22% damaged) and reached a plateau at 1 mT (30% damaged).
On the contrary, the exposure of spermatozoa to extremely low frequency electromagnetic field (all intensities) did not affect the DNA integrity,
Under in vivo conditions, the extremely low frequency electromagnetic field of intensity of 1 mT significantly reduced the fertilization rate. A decreased fertilization rate was found in absence of spermatozoa at exposure application (protocol B; 80% versus 95% in controls) that resulted more evident when the oviducts were exposed in presence of spermatozoa (protocol A; 68% versus 80% in controls). On the contrary, the polyspermy rate was unaffected in both protocols.
In addition, the exposure of oviducts (≥ 0.75 mT) in the absence of spermatozoa was able to negatively affect early embryo development (a slowdown in the embryo cleavage was found).
In conclusion, it was demonstrated how and at which intensities the extremely low frequency electromagnetic field negatively affect early fertility outcome in a highly predictive animal model.
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