Objective Identification of Human Sperm Hyperactivation by Computerized Sperm Motion Analysis

Computerized Sperm Motility Analyzer를 이용한 Human Sperm의 Hyperactivated Motility의 객관적 관찰에 관한 연구

  • Lee, Hee-Kyung (Department of Obstetrics and Gynecology, Medical College, Korea University) ;
  • Lee, Chan (Department of Obstetrics and Gynecology, Medical College, Korea University) ;
  • Kim, Hyun-Sook (Department of Obstetrics and Gynecology, Medical College, Korea University) ;
  • Kim, Young-Tae (Department of Obstetrics and Gynecology, Medical College, Korea University) ;
  • Kim, Sun-Haeng (Department of Obstetrics and Gynecology, Medical College, Korea University) ;
  • Ku, Pyoung-Sahm (Department of Obstetrics and Gynecology, Medical College, Korea University)
  • 이희경 (고려대학교 의과대학 산부인과학교실) ;
  • 이찬 (고려대학교 의과대학 산부인과학교실) ;
  • 김현숙 (고려대학교 의과대학 산부인과학교실) ;
  • 김영태 (고려대학교 의과대학 산부인과학교실) ;
  • 김선행 (고려대학교 의과대학 산부인과학교실) ;
  • 구병삼 (고려대학교 의과대학 산부인과학교실)
  • Published : 1994.04.30

Abstract

The occurrence and time course of capacitation, acrosomal loss, and hyperactivated motility require quantitative definition in order to characterize fertile human sperm. Recently the method has been developed to estimate the quality of spermatozoa by using kinematic parameters such as curvilinear velocity(VCL), average path velocity(VAP), linearity(LIN), straightness(STR), amplitude of lateral head displacement(ALH), and beat cross frequence(BCF) from Computer Assisted Sperm Analysis (CASA). In this study, using the Hamilton Thorn motility analyzer HTM 2030(Hamilton Thorn Research, Beverly, MA), we attempted to identify the spermatozoa with hyperactivated motility (HA) objectively and to monitor hyperactivation of human spermatozoa during incubation in capacitating media and after treatment of calcium ionophore as compared with acrosome status. And we examined whether HA are related to the result of SPA. Semen samples obtained from 16 healthy men were prepared by swim up technique and preincubated in a capacitating media(modified BWW medium) for 5 hours and treated with calcium ionophore solution. The acrosome reaction was detected with PSA-FITC labelling of the acrosome and in vitro sperm ferilizing capacity was assessed by the zona free hamster ovum penetration assay (SPA). The incidence of hyperactivated sperm was 2.6% in fresh semen, 14.3% of the swim up population, 13.7% after 5h of incubation. Significant increase of percentage of hyperactivated sperm was observed after the incubation (p<0.05) but after treatment, no significant changes of percentage of hyperactivated sperm(l1.8%) in contrast to significant rise in the percentage of acrosome reacted cells. Correlation analysis failed to show any significant relationship between the percentage of sperm with HA and SPA score. In conclusion, although no direct correlations were found between the results of SPA and HA, hyperactivation of sperm is associated with capacitation and monitoring hyperactivated sperm will be expected as a method of evaluating the functional quality of sperm such as SPA.

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