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过氧化氢对生育男性精子凋亡及核DNA完整性的影响
引用本文:韩艳君,郑贤红,王一男,侯元,戴汝琳,刘睿智.过氧化氢对生育男性精子凋亡及核DNA完整性的影响[J].中国优生与遗传杂志,2009,17(5):126-127.
作者姓名:韩艳君  郑贤红  王一男  侯元  戴汝琳  刘睿智
作者单位:韩艳君,HAN Yan-jun(吉林大学第二医院手术室,吉林,长春,130041);郑贤红,王一男,戴汝琳,刘睿智,ZHENG Xian-hong,HOU Yuan,DAI Ru-lin,LIU Rui-zhi(吉林大学白求恩医学院细胞生物学教研室,吉林省生殖医学研究所,吉林,长春,130021);侯元,EANG Yi-nan(吉林大学白求恩医学院中心实验室,吉林,长春,130021)  
基金项目:吉林省科技厅资助项目 
摘    要:目的研究体外过氧化氢对生育男性精子凋亡及精子DNA完整性的影响。方法58例正常生育男性均来自吉林大学第二临床医院泌尿男科,精子Percoll优选后制作精子悬液,用伊红Y染色分析精子活率,用瑞-姬染色分析精子凋亡率,用精子核吖啶橙荧光染色检测精子DNA完整性。结果外加过氧化氢浓度为0.02mmol/l时,精子活率显著低于对照组(P〈0.05)。当浓度为0.20mmol/l时,精子活率显著低于对照组(P〈0.05),精子凋亡率显著高于对照组(P〈0.05)。外加过氧化氢浓度为0.02mmol/l、0.2mmol/l时,精子DNA完整性均显著低于对照组(P〈0.05),且精子DNA完整性随实验浓度增加而下降。结论体外过氧化氢对精子活率、凋亡率与DNA完整性有影响,高浓度的过氧化氢可促使精子凋亡,损伤精子DNA完整性,导致男性不育。

关 键 词:过氧化氢  精子凋亡  精子DNA完整性

Influence of H2O2 in vitro on human sperm viability and DNA integrity of fertile male
HAN Yan-jun,ZHENG Xian-hong,HOU Yuan,EANG Yi-nan,DAI Ru-lin,LIU Rui-zhi.Influence of H2O2 in vitro on human sperm viability and DNA integrity of fertile male[J].Chinese Journal of Birth Health & Heredity,2009,17(5):126-127.
Authors:HAN Yan-jun  ZHENG Xian-hong  HOU Yuan  EANG Yi-nan  DAI Ru-lin  LIU Rui-zhi
Institution:HAN Yan -jnn, ZHENG Xian - hong, HOU Yuan, EANG Yi -nan, DAI Ru -lin, LIU Rui -zhi. (Department of Cell Biology, Norman Bathune Medicine College, Jilin University, Changchun, 130021, China)
Abstract:Objective: To study effect of H2O2 in vitro on human sperm viability and DNA integrity of fertile male. Methods: Semen samples were obtained from 58 fertile male in department of urology, the second hospital, Jilin University. Sperm viability was detected by eosin - Y staining. The semen smears were stained by Wright - Giemsa staining for analyzing spermapoptosis rate. Sperm DNA integrity was detected by sperm nucleus acridine orange fluorescence staining. Results: When H2O2 concentration in vitro was 0. 02mmol/l, sperm viability was markedly lower than that of control group ( P 〈 0. 05 ). When it was 0. 02mmol/l, sperm viability was markedly lower than that of control group ( P 〈 0. 05 ), sperm apoptosis rate were markedly higher than that of control group ( P 〈 0. 05 ). When it were 0. 02mmol/l, 0. 2mmol/l, sperm DNA integrity was both markedly lower than that of control group ( P 〈 0. 05 ). With H2O2 concentration increasing, sperm DNA integrity was descending. Conclusion: H2O2 in vitro influence on sperm viability, sperm apoptosis rate and DNA integrity. H2O2 of high concentration could make sperm apoptosis, and damage sperm DNA integrity.
Keywords:H2O2  Sperm apoptosis  Sperm DNA integrity
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