目的:利用荧光探针JC-1观察氧化应激对精子线粒体膜电位的变化。方法:用FeSO4/H2O2体系诱导精子氧化损伤模型,利用新型荧光探针JC-1标记精子线粒体,在FACS Calibur流式细胞仪上检测JC-1荧光强度的变化。结果:正常精子线粒体维持较高的膜电位,JC-1在线粒体内形成聚合物,红色荧光占主导地位。VeSO4/H2O2体系导致线粒体膜电位下降,JC-1聚合物分解成单体,红色荧光强度减弱。结论:氧化应激导致精子线粒体膜电位下降;JC-1结合流式细胞仪是一种理想的检测线粒体膜电位的手段。
Objective: To explore the changes of mitochondrial membrane potential(MMP) in sperms in oxidative stess model with fluorescent JC-1. Methods: FeSO4/H2O2 system was used to induce sperm model of oxidative injury, and JC-1 in combination with flow cyometry was used to detect the changes of sperm MMP in the exposure of reactive oxygen species(ROS). Results: Normal sperms had a high MMP, and JC-1 aggregates were formed in the inner membranes of mitochondria and emitted orange-red fluorescence. ROS caused the decrease of MMP, and JC-1 aggregates were dissociated to monomer which emitted green fluorenscence. Conclusions: Oxidative stress can cause the decrease of MMP; JC-1 in combination with flow eytometry is an ideal method to detect the change of mitochondrial membrane potential.