The present study tested the effects of Wi-Fi (2.45 GHz for 1h) exposure on Ca(2+) influx, oxidative stress and apoptosis through TRPV1 channel in the murine dorsal root ganglion (DRG) and hippocampus of pentylentetrazol (PTZ)-induced epileptic rats. The cytosolic free Ca(2+), reactive oxygen species production, apoptosis, mitochondrial membrane depolarization, caspase-3 and -9 values in hippocampus were higher in the PTZ group than in the control although cell viability values decreased. The Wi-Fi exposure induced additional effects on the cytosolic Ca(2+) increase. However, pretreatment of the neurons with CPZ, results in a protection against epilepsy-induced Ca(2+) influx, apoptosis and oxidative damages. In conclusion, epilepsy and Wi-Fi in our experimental model is involved in Ca(2+) influx and oxidative stress-induced hippocampal and DRG death through activation of TRPV1 channels, and negative modulation of this channel activity by CPZ pretreatment may account for the neuroprotective activity against oxidative stress.
Studies have shown an association between cell phone use and a decreased risk of certain brain tumors. According to a peer-reviewed Dec. 2006 study of 420,095 cell phone users in Denmark, the results showed a "reduced brain tumor risk" among long-term subscribers.  Two other peer-reviewed studies also found that cell phone users had a slightly decreased risk of developing brain tumors. A July 20, 2005 Danish study  found a "decreased risk for high-grade glioma," a malignant brain tumor, and a 2005 Swedish study  also found a "decreased odds ratio" for developing glioma as well as meningioma, another type of brain tumor.
Ionizing radiation, including x-rays and ultraviolet light, produces molecules called ions that have either too many or too few electrons. Ions are known to damage DNA and cause cancer. Cell phone radiation, like radio, TV, and visible light radiation, is non-ionizing and lacks sufficient energy to add or remove electrons from molecules, and therefore it cannot ionize and cause cancer.  According to the authors of a 2005 peer-reviewed study of 3.7 million Swedish residents, a "biologic mechanism that could explain any possible carcinogenic effect from radiofrequency radiation has not been identified." 
The aim of this study was to investigate electromagnetic radiation (EMR) transmitted by wireless devices (2.45 GHz, 3h/day for 30 days), which may cause physiopathological or ultrastructural changes, in the testes of rats and address if the supplemental gallic acid (GA) may reduce these adverse effects. EMR only group was shown to have higher oxidative stress, decreased testosterone and VEGF levels, increased prostaglandin E2 and CGRP, as well as decreased numbers of spermatozoa. Long term EMR exposure resulted in testicular physiopathology via oxidative damage and inflammation. GA may have ameliorative effects on the prepubertal rat testes physiopathology.
There was a negative correlation between the cell phone usage duration and the total sperm count (r = −0.064, p = 0.04). Similarly, there was also a negative correlation between the wireless internet usage duration and the total sperm count (r = −0.089, p = 0.019). Otherwise there were no significant correlations among the other four main question branches (cell phone usage time, cell phone carriage habits, wireless internet usage time. and internet connection type) and sperm parameters.
In a separate study by the same Swedish team, they found more than seven times the risk among people using a cell phone more than 20 years and 6.5 times the risk for long-term users of cordless phones. As expected, most of the gliomas and acoustic neuromas were on the same side of the head, which was usually exposed to the phone. In the 2013 official report on the medical evidence for brain tumors, the International Agency for Research on Cancer concluded that radiation from cell phones is “possibly carcinogenic to humans”.