JRI 

Tahmineh Peirouvi
- Department of Histology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran
Maerefat Ghaffari Corresponding Author
- Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran
Jafar Soleimanirad
- Anatomy Department, Faculty of Medicine, Tabriz Medical Sciences University, Tabriz, Iran
Laeya Farzadi
- Department of Obstet . and Gynecol . of Tabriz University of Medical Science, Tabriz, Iran

Received: 7/1/2004 Accepted: 7/1/2004 - Publisher : Avicenna Research Institute

Related Articles

 

Other Format

 


Abstract

Introduction: Acrosome is a cap-like structure which contains several hydrolytic enzymes necessary for acrosome reaction. Generally, acrosome reaction would be important if it occured on the zona pellueida, other wise; the spermatozoa could not penetrate through this layer. On the other hand, freezing- thawing process can damage acrosome membrane and reduce the sperm fertilizing potential. There is little information about the effects of vapor phase cryopreservation on acrosome. The aim of the persent study is to evaluate the effect of vapor phase cryopreservation on acrosome of spermatozoa of subfertile and fertile men. Materials and Methods: In this study, semen samples were collected from subfertile (n=20) and fertile men (n=10) after 48 h abstinence of intercourse. After semen analysis by Semen Analyzer Quality according to WHO criteria, each semen sample was divided into two portions (100 µl each). The first portion was stained with triple staining to show the quality of acrosome and the second portion was stained after vapor phase cryopreservation and thawing. Results were analyzed by paired t-test. Results: Before vapor phase cryopreservation, mean percentage of live spermatozoa with intact acrosome in subfertile men and fertile men were 26±3.64 and 33.37±4.07, respectively, but it decreased following vapor phase cryopreservation-thawing to 11.6±1.82 in subfertile and 9.87±2.97 in fertile men. Conclusion: It is concluded that vapor phase cryopreservation, impairs acrosome structure and causes destruction of acrosome and extrudes acrosomal enzymes in absence of oocyte. Therefore cause reduction of fertility of spermatozoa in fertile and subfertile men.


Keywords: Acrosome, Vapor phase cryopreservation, Sperm, Fertility, Infertility, Assisted Reproductive Techniques


To cite this article:


References

  1. Baldi E., Luconi M., Bonaccorsi L., et al. Human sperm activation during capacitation and Acrosome Reaction. Bioscience.1996;1:189-205.
  2. Purohit B.S., Laloraya M., Kumar P.G. Role of ions and ion channels in capacition and acrosome reaction of spermatozoa. Asian J Androl.1999;3:95-107.
  3. Fenichel P., Donzeau M., Farahifar D. Dynam- ics of human sperm acrosome reaction, relation with in vitro fertilization. Fertil Steril.1991;55: 994-9.
  4. Michaut M., Tomes C.N., De Blas G., Yunes R., Mayorga L.S. Calciumtriggered acrosomal exocytosis in human spermatozoa requires the coordinated activation of Rab3A and N ethylmal- eimidesensitive factor. Natl Acad Sci.2000;97: 9996-10001.
  5. Rossato M., Virgilio F., Rizzuto R., Galeazzi C., Foresta C. Intracellular calcium store depletion and acrosome reaction inhuman spermatozoa: role of calcium and plasma membrane potential. Mol Hum Reprod.2001;7:119-28.
  6. Michaut M., De Blas G., Tomes C.N., Yunes R., Fukuda M., Mayorgal S: Synaptotagmin VI participates in the acrosome reaction of human spermatozoa. Dev Biol.2001;235:521-9.
  7. De Jonge C.J., Rawlins R.G., Zaneveld L.J. Induction of the human sperm acrosome reac- tion by human oocytes. Fertil Steril.1988;50: 949-951.
  8. Milligan S.R. Mammalian sperm interacttion with extracellular matrices of the egg. In Oxford Review of Reproduction Biology. Oxford Univer- sity Press, Oxford.1989;pp:339-88.
  9. Foresta C., Rossato M., Virgilio F. Extracellul-ar ATP is a trigger for the acrosome reaction in human spermatozoa. J Biol Chem.1992;267: 19443-7.
  10. Tomiyama T., Ohashi K., Tsutsui T., Saji F., Tanizawa O. Acrosome reaction induced in a limited population of human spermatozoa by progesterone (Ca2+-dependent) and ATP (CA2+-independent). Hum Reprod.1995;10:2052-5.
  11. World Health Organization (WHO) laboratory manual for the examination of human semen and semenservical mucus interaction, 4th Edition, Cambridge University Press, Cambridge.1999; pp:6-23.
  12. Talbot P., Chacon R.S. A triple stain techni- que for evaluating normal acrosome reactions of human sperm. J Exp Zoll.1981;215:20-8.
  13. Hammadeh M., George T., Baum R. Schmidt W. Association between freezing agent and acro-some damage of human spermatozoa from sub-normal and normal semen. Andrology.2001;33: 331-6.
  14. Vayena E., Rowe P., Griffin P. Current practices and controversies in Assisted Rep- roduction. WHO, Geneva.2002;152-65.
  15. Donnelly E.T., Steele E.K., McClure N., Lewis S.E. Assessment of DNA integrity and morphology of ejaculated spermatozoa from fertile and infertile men before and after cryo-preservation. Hum Reprod.2001;16:1191-9.
  16. Esteves S.C., Spaine D.M., Cedenho A.P., Srougi M. Effects of the technique of cryopre-servation and dilution/centrifugation after that-hawing on the motility and vitality of spermato-zoa of oligoasthenozoospermic men. Int Braz J Urol.2003;29:133-40.
  17. Cross N.L., Hanks S.E. Effects of cryopr-eservation on human sperm acrosomes. Hum Reprod.1991;6:1279-83.
  18. Check M.L., Check J.H., Long R. Detrimental effects of cryopreservation on structural and func-tional integrity of the sperm membrane. Arch Androl.1991;27:155-60.
  19. Hammerstedt R.H., Graham J.K., Nolan J.P. Cryopreservation of mammalian sperm: what we ask them to survive. J Androl.1990;11(1):73-88.
  20. Alvarez J.G., Storey B.T. Evidence of increa-sed lipid peroxidase damage and loss of super- oxide dismutase activity as a mode of sublethal cryodamage to human sperm during cryopreser-vation. J Androl.1992;13(3):232-41.
  21. Drobnis E.Z., Clisham P.R., Brazil C.K., Wisner L.W., Zhong C.Q., Overstreet J.W. Detection of altered acrosomal physiology of cryopreserved human spermatozoa after sperm residence in the female reproductive tract. J Reprod Fertil.1993;99(1):159-65.
  22. Hammadeh M., Askari A., Georg T., Rosen-baum P., Schmidt W. Effect of freezethawing procedure on chromatin stability, morphological alteration and membrane integrity of human sper-matozoa in fertile and subfertile men. J Androl. 1999;22(3):155-62.
  23. Kotwicka M., Jendraszak M., Warchol J. Changes in actin localization after acrosome reaction in human spermatozoa. Cell Mol Biol. 2002;7:290.
  24. Stanic P., Tandare M., Sonicki Z., Simunic V., Radakovic B., Suchanek E., Comparison of protective media and freezing techniques for cryopreservation of human semen. Eur J Obstet Gynecol Reprod Biol.2000;91(1):65-70.
  25. Hammadeh M., Greiner S., Rosenbaum P., Schmidt W. Comparison between human sperm preservation medium and TESEYolk buffer on protecting chromatin and morphology integrity of human spermatozoa in fertile and subfertile men after freezethawing procedure. J Androl. 2001; 22(6):1012-8.
  26. Donnelly E.T., McClure N., Lewis S.E. Cryo-preservation of human semen and prepared sperm: effects on motility parameters and DNA integrity. Fertil Steril.2001;76(5):892-900.
  27. Buhr M.M., Curtis E.F., Somnpan Kakuda N. Composition and behavior of head membrane lipids of fresh and cryopreserved boar sperm. Cryobiol.1994;31(3):224-38.
  28. Nolan J.P., Hammerstedt R.H. Regulation of membrane stability and the acrosome reaction in mammalian sperm. FASEB J.1997;11(8):670-83.
  29. Okada A., Igarashi H., Kuroda M., Terao K., Yoshikawa Y., Sankai T. Cryopreservation indu-ced acrosomal vesiculation in live spermatozoa from cynomolgus monkeys(Macaca Fascicularis), Hum Reprod.2001;16(10):2139-47.

COPE
SID
NLM
AJMB
IJBMLE
IJBMLE

Home | About Us | Current Issue | Past Issues | Submit a Manuscript | Instructions for Authors | Subscribe | Search | Contact Us

"Journal of Reproduction & Infertility" is owned, published, and managed by Avicenna Research Institute .
Creative Commons License

This work is licensed under a Creative Commons Attribution –NonCommercial 4.0 International License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.

Journal of Reproductoin and Infertility (JRI) is a member of COMMITTEE ON PUBLICATION ETHICS . Verify here .

©2024 - eISSN : 2251-676X, ISSN : 2228-5482, For any comments and questions please contact us.