首页 | 本学科首页   官方微博 | 高级检索  
     

正常精子体外与活性氧作用后超微结构观察
引用本文:商学军,黄宇烽,熊承良,印洪林,王咏梅. 正常精子体外与活性氧作用后超微结构观察[J]. 中华男科学杂志, 2002, 8(2): 106-108
作者姓名:商学军  黄宇烽  熊承良  印洪林  王咏梅
作者单位:1. 南京军区南京总医院生殖遗传研究室,江苏,南京,210002
2. 华中科技大学同济医学院计划生育研究所
3. 南京军区南京总医院病理科,江苏,南京,210002
基金项目:江苏省生殖医学重点实验室开放课题资助 (K990 62 )
摘    要:
目的 :观察精子与活性氧 (ROS)作用后超微结构变化。 方法 :采用Percoll梯度离心法选择具有正常生理功能的精子作为正常精子模型 ,应用次黄嘌呤 黄嘌呤氧化酶体系产生ROS ;在有氧环境下ROS与精子模型孵育后 ,采用透射电镜观察精子超微结构。 结果 :正常精子模型与ROS作用后 ,精子膜及顶体存在不同程度的损伤 ,精子线粒体结构出现异常。 结论 :过多的ROS可致精子膜、顶体以及线粒体的超微结构改变 ,损害精子功能。

关 键 词:精子  活性氧  超微结构  体外
文章编号:1009-3591(2002)02-0106-03
修稿时间:2001-08-20

Ultrastructural Observation of Normal Spermatozoa Incubated with ROS in vitro
Xue Jun SHANG ,Yu Feng HUANG ,Cheng Liang XIONG ,Hong Lin YIN ,Yong Mei WANG. Ultrastructural Observation of Normal Spermatozoa Incubated with ROS in vitro[J]. National journal of andrology, 2002, 8(2): 106-108
Authors:Xue Jun SHANG   Yu Feng HUANG   Cheng Liang XIONG   Hong Lin YIN   Yong Mei WANG
Affiliation:Laboratory of Reproduction & Genetics, Nanjing General Hospital of Nanjing Command, PLA, Nanjing, Jiangsu 210002, China.
Abstract:
Objectives: To observe ultrastructural changes of spermatozoa after incubate with reactive oxygen species ( ROS ). Methods: Spermatozoa of normal physiological functions selected from semen samples by Percoll gradient centrifugation technique were regarded as normal sperm models in present study. Ultrastructural changes of spermatozoa observed by transmission electron microscope after model spermatozoa were incubated with ROS generated by hypoxanthine and xanthine oxidase under aerobic environment. Results: After model spermatozoa were incubated with ROS, impairment of various extent in membrane and acrosome of spermatozoa and abnormality in mitochondria of spermatozoa were found. Conclusions: Excessive ROS may cause ultrastructural change in membrane, acrosome and mitochondria of spermatozoa and impair function of spermatozoa.
Keywords:Spermatozoa  Reactive oxygen species  Ultrastructure  in vitro
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号