The effect of non thermal 900 MHZ mobile phone radiation on human spermatozoa

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dc.contributor.advisor Huyser, Carin en
dc.contributor.advisor Franken, Daniel R. en
dc.contributor.advisor Leszczynski, Dariusz en
dc.contributor.postgraduate Falzone, Nadia en
dc.date.accessioned 2013-09-06T18:09:29Z
dc.date.available 2008-06-02 en
dc.date.available 2013-09-06T18:09:29Z
dc.date.created 2007-11-23 en
dc.date.issued 2008-06-02 en
dc.date.submitted 2008-05-15 en
dc.description Thesis (PhD (Reproductive Biology))--University of Pretoria, 2008. en
dc.description.abstract Several studies have highlighted the possibility that radio-frequency electromagnetic fields (RF-EMF) used in mobile phone technology could influence DNA integrity of male germ cells as well as sperm motility. Current knowledge concerning the influence of RF-EMF on male germ cells is extremely limited. In the present study the hypothesis that 900 MHz GSM radiation could induce the activation of stress response in human spermatozoa was investigated. Ejaculated, density purified, human spermatozoa from donors were exposed to 900 MHz GSM mobile phone radiation at specific absorption rate (SAR) levels of 2.0 and 5.7 W/kg and examined at various time points post exposure. Sperm motility and morphology were evaluated by computer-aided sperm analysis (CASA). The ability of RF-EMF exposed sperm to undergo the acrosome reaction was evaluated by flow cytometry. Sperm binding to the zona pellucida of human oocytes was determined by the hemi-zona (HZA) assay. Apoptotic markers, phosphatidylserine (PS) externalization, change in mitochondrial membrane potential (Δψm), reactive oxygen species (ROS) generation, caspase activation and DNA fragmentation were analysed using flow cytometry. Heat shock protein (Hsp) 27 and 70 expression and activity were analyzed using specific antibodies with flow cytometry and Western blot methods. Stress fibre stabilization (F-actin polymerization) was visualized using fluorescent dye labelled phalloidin. No effect was seen on kinematic parameters assessed at SAR 2.0 W/kg, however straight line velocity (VSL) and beat cross frequency (BCF) were significantly altered after exposure at SAR 5.7 W/kg. Sperm shrinkage (decrease in surface area) was observed at both exposure levels. RF-EMF did not influence exposed spermatozoa’s ability to undergo the acrosome reaction. A significant decrease in sperm-zona binding was observed at both exposure levels. RF radiation did not have an effect on any apoptotic markers. ROS generation increased significantly with an increase in SAR (5.7 W/kg). RF-EMF did not induce a stress response in exposed sperm (no activation of Hsp70 and 27 activity). These results cannot be ascribed to heating, as the temperature did not increase by more than 0.2 - 0.3ºC during exposure. The decrease in sperm-zona binding is the result of an alternative non-stress inducible pathway. This study should be replicated at lower SAR levels that would simulate the radiation absorption from carrying the cell phone in a pocket close to the testes. en
dc.description.availability unrestricted en
dc.description.department Obstetrics and Gynaecology en
dc.identifier.citation a, en
dc.identifier.other 2007 en
dc.identifier.upetdurl http://upetd.up.ac.za/thesis/available/etd-05152008-112158/ en
dc.identifier.uri http://hdl.handle.net/2263/24680
dc.language.iso en
dc.publisher University of Pretoria en_ZA
dc.rights © University of Pretoria, 20 en
dc.subject Apoptosis en
dc.subject Human spermatozoa en
dc.subject Mobile phone radiation en
dc.subject Sperm functionality en
dc.subject Stress response en
dc.subject UCTD en_US
dc.title The effect of non thermal 900 MHZ mobile phone radiation on human spermatozoa en
dc.type Thesis en


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