College of Biotechnology, Mathura, India.
UP Pandit Deen Dayal Upadhyaya Pashu Chikitsa Vigyan Vishwavidyalaya (Veterinary University), Mathura, 281001, Uttar Pradesh, India.
Sci Rep. 2021 Jan 12;11(1):646. doi: 10.1038/s41598-020-80235-y.
Earlier we have reported mercury-induced alterations in functional dynamics of buck spermatozoa through free radicals-mediated oxidative stress and spontaneous acrosome reaction. Based on our earlier findings, we aimed to investigate the effect of mercury exposure on motility, kinematic patterns, DNA damage, apoptosis and ultra-structural alterations in goat spermatozoa following in vitro exposure to different concentrations (0.031-1.25 µg/ml) of mercuric chloride for 15 min and 3 h. Following exposure of sperm cells to 0.031 µg/ml of mercuric chloride for 3 h, livability and motility of sperms was significantly reduced along with altered kinematic patterns, significant increase in per cent necrotic sperm cells and number of cells showing DNA damage; and this effect was dose- and time-dependent. Contrary to up-regulation of Bax gene after 3 h in control group, there was significant increase in expression of Bcl-2 in mercury-treated groups. Transmission electron microscopy studies revealed rifts and nicks in plasma and acrosomal membrane, mitochondrial sheath, and collapsed mitochondria with loss of helical organization of mitochondria in the middle piece of spermatozoa. Our findings evidently suggest that mercury induces necrosis instead of apoptosis and targets the membrane, acrosome, mid piece of sperms; and the damage to mitochondria seems to be responsible for alterations in functional and kinematic attributes of spermatozoa.
早些时候,我们通过自由基介导的氧化应激和自发顶体反应报告了汞对buck 精子功能动力学的改变。基于我们早期的研究结果,我们旨在研究在体外暴露于不同浓度(0.031-1.25µg/ml)氯化汞 15 分钟和 3 小时后,汞暴露对山羊精子活力、运动学模式、DNA 损伤、凋亡和超微结构改变的影响。在将精子细胞暴露于 0.031µg/ml 的氯化汞 3 小时后,精子的存活率和活力明显降低,运动学模式发生改变,坏死精子的百分比显著增加,显示 DNA 损伤的细胞数量也增加;这种影响是剂量和时间依赖性的。与对照组 3 小时后 Bax 基因的上调相反,在汞处理组中 Bcl-2 的表达显著增加。透射电子显微镜研究显示,在精子的质膜、顶体膜、线粒体鞘和中段中,出现了裂痕和缺口,线粒体崩溃,其中线粒体的螺旋结构丢失。我们的研究结果清楚地表明,汞诱导的是坏死而不是凋亡,并且靶向精子的膜、顶体、中段;而线粒体的损伤似乎是导致精子功能和运动学特性改变的原因。