Hanafi, N., Eid, F., El- Dahshan, A. (2012). Radiation Emitted From Mobile Phone Induces Amyloidosis Features in Some Tissues of Infant Mice. The Egyptian Journal of Hospital Medicine, 47(1), 132-144. doi: 10.21608/ejhm.2012.16287
N Hanafi; F. Eid; A. El- Dahshan. "Radiation Emitted From Mobile Phone Induces Amyloidosis Features in Some Tissues of Infant Mice". The Egyptian Journal of Hospital Medicine, 47, 1, 2012, 132-144. doi: 10.21608/ejhm.2012.16287
Hanafi, N., Eid, F., El- Dahshan, A. (2012). 'Radiation Emitted From Mobile Phone Induces Amyloidosis Features in Some Tissues of Infant Mice', The Egyptian Journal of Hospital Medicine, 47(1), pp. 132-144. doi: 10.21608/ejhm.2012.16287
Hanafi, N., Eid, F., El- Dahshan, A. Radiation Emitted From Mobile Phone Induces Amyloidosis Features in Some Tissues of Infant Mice. The Egyptian Journal of Hospital Medicine, 2012; 47(1): 132-144. doi: 10.21608/ejhm.2012.16287
Radiation Emitted From Mobile Phone Induces Amyloidosis Features in Some Tissues of Infant Mice
1Radiation Biology Department, National Centre for Radiation Research and Technology (NCRRT), Atomic Energy Authority (AEA), Cairo, Egypt.
2Zoology Department, Faculty of Science for Girls, Al-Azhar University, Cairo, Egypt.
Abstract
Aim: Investigating the effects of mobile phone–emitted radiation (MPR) on inducing histopathological changes associated with amyloidosis feature in liver, kidney and brain of infant mice. Methods: Twenty one infant mice (aged 1 day) were assigned to 3 groups, the 1st group served as control, the 2nd group exposed to mobile phone radiation ( MPR) daily for one month (¾ h /day) and the 3rd group remained for one month after stopping radiation exposure. Results: There were different degrees of damage related to amyloidosis feature in these organs subsequent to MPR exposure. One month post exposure there was an increase in the degree of damage related to amyloidosis feature. Conclusion: the results of this study showed that MPR leads to histopathological changes associated with amyloidosis feature in the liver, kidney and brain of infant mice.