Author/Authors :
Syamsunarno, Mas Rizky A.A Working Group of Genetic Medicine - Faculty of Medicine - Universitas Padjadjaran, Jatinangor, Indonesia , Widyastuti, Rini Central Laboratory - Universitas Padjadjaran, Jatinangor, Indonesia , Herlambang, Herlambang Faculty of Medicine and Health Sciences - Universitas Jambi, Jambi, Indonesia , Lubis, Alkaustariyah Working Group of Genetic Medicine - Faculty of Medicine - Universitas Padjadjaran, Jatinangor, Indonesia , Ghozali, Mohammad Working Group of Genetic Medicine - Faculty of Medicine - Universitas Padjadjaran, Jatinangor, Indonesia , Panigoro, Ramdan Working Group of Genetic Medicine - Faculty of Medicine - Universitas Padjadjaran, Jatinangor, Indonesia
Abstract :
Background: Iron is an essential substrate in the body and needed in a small amount. In iron overload
condition, such as patients who undergo routine blood transfusion for a long period, there is a risk of iron toxicity and
affect fertility, signed by hypogonadism and reduction of sperm quality. However, the effect of short-term iron overload in the reproductive organ is not clearly understood. This study is conducted to determine the effect of short term
iron administration to the male reproductive organ, testosterone, and epididymis sperm quality. Methods: Mice were
injected with iron dextran intraperitoneally by the doses of 0, 0.05, 0.1, and 0.3 mg/day for 18 days. The reproductive
organ, blood, and epididymis sperm were collected at the end of the treatment.
Results: Epididymis-body weight ratio was decreased and the seminal vesicle-body weight ratio was increased in
iron dextran treatment group compare to control (p<0.05). The interstitial seminiferous tubules in testis showed the
accumulation of debris cells and thickening of epithelial. and the seminiferous intratubular filled with fibrin deposit
and disintegrated of spermatogenic cell. There was a significant increase in sperm concentration (p<0.05) and sperm
motility rate in the iron dextran treated-group. Furthermore, the testosterone serum level was increased in treatment
groups in a dose-dependent manner, although the difference was not statistically significant (p>0.05).
Conclusion: Short term iron overload alters the male mice reproduction showed by disruption in testis and increase
of epididymis sperm concentration and motility (p<.0.05)
Keywords :
Iron overload , Sperm quality , Testis , Testosterone , Histopathology