ABSTRACT
Background: methamphetamine [MA] was shown to have harmful effects on male reproductive system
Objective: to investigate probable effects of daily administration of MA on sperm parameters and chromatin/DNA integrity in mouse
Material and Methods: thirty-five NMRI male mice were divided into five groups including low, medium, and high dosage groups which were injected intraperitoneally with 4, 8 and 15 mg/kg/day for 35 days, respectively. Normal saline was injected in sham group and no medications were used in control group. Then, the mice were killed and caudal epididymis of each animal was cut and placed in Ham's F10 medium for sperm retrieval. To evaluate sperm chromatin abnormalities, the aniline blue, toluidine blue and chromomycine A3 were used. For sperm DNA integrity and apoptosis, the acridine orange, sperm chromatin dispersion, and TUNEL assay were applied. For sperm morphology, Papanicolaou staining was done
Results: normal morphology and progressive motility of spermatozoa decreased in medium and high dosage groups in comparison with the control group [p=0.035]. There was a significant increase in rate of aniline blue, toluidine blue, and chromomycine A3 positive spermatozoa in high dosage group. In a similar manner, there was an increase in rates of acridine orange, TUNEL and sperm chromatin dispersion positive sperm cells in high dosage group with respect to others
Conclusion: MA abuse in a dose-dependent manner could have detrimental effects on male reproductive indices including sperm parameters and sperm chromatin/DNA integrity in mice
ABSTRACT
Background: The particles in the range of 1-100 run are called nanoparticles. Gold nanoparticle is one of the most important metal nanoparticles with wide usage
Objective: This study investigated the effects of gold nanoparticles on sperm parameters and chromatin structure in mice
Materials and Methods: In this experimental study, 72 male bulb-c mice were divided into 9 groups including: ;4 Sham groups [Sc 1-4], 4 experimental groups [Au 1-4], and 1 control group [C]. Experimental groups received 40 and 200 fig/kg/day soluble gold [Au] nano-particles for 7 and 35 days, by intra peritoneal injection, respectively. Sham groups were treated with 1.2 rnM sodium citrate solution with 40 and 200 jag/kg/day doses for same days and control group did not receive any materials. Motility and Morphology of spermatozoa were analyzed. Chromatin quality was also evaluated using AB [Aniline blue], TB [Toluidine blue] and CMA3 [Chromomycin A3] staining methods
Results: The sperm analysis results showed that motility and morphology of sperm in experimental groups [especially in groups that have been treated for 35 days with nano-particles] had significant decrease in comparison with control group. TB, AB and CM A3 results showed a significant increase in abnormal spermatozoa from all Au-treated groups
Conclusion: Gold nano-particles firstly can reduce the sperm parameters such as motility and normal morphology and secondly affect sperm chromatin remodeling and cause the increase instability of chromatin and also increase the rate of sperm DNA damage. These deleterious effects were more obvious in maximum dose and chronic phase