Cover
Vol. 2 No. 1 (2012)

Published: June 30, 2012

Pages: 26-30

Research Article

In vitro sperm activation using culture medium supplied with oxytocin in asthenozoospermic patients

Abstract

Background: Pretreatment of the semen samples of the asthenozoospermia patients with certain sperm stimulant agents prior to use for assisted reproductive techniques (ART) has been reported to have beneficial effects on fertilization rates. Objectives: Investigating the influence of addition of different concentrations of oxytocin (OT) to semen samples of asthenozoospermic patients for in vitro sperm activation as a new method for stimulation of sperm motility in these patients and exploring the concentration of OT that harvests amaximal numberofmotile sperms. Methods: Simple layer technique for in vitro sperm activation using culture medium enriched with OT was studied in asthenozoospermic patients (No. 90). Semen samples were examined before sperm activation, and then they were divided into three equal groups. In the first group, three concentrations of OT (2, 4, and 6 IU/ml) were applied. Based on the results of the mentioned work, OTat the concentration of 2 IU/mlwas applied with sperm preparation medium (SPM) and without in the second and third groups, respectively. Results: Results showed that there was a significantimprovementin the percentageof sperm motilityand spermgrade activity of the OT-treated samples atthe concentration of 2IU/mlas comparedto the control samples. Moreover, there was a tendency for a decrease in sperm grade activity with increase OT concentration. The outcome of sperm activation in presence of SPM revealed a significant increase in the sperm motility characteristics (the percentage of sperm motility and sperm grade activity) in the control and OT-treated samples and the best improvement in these sperm motility characteristics was observed in the OT-treated samples. When SPM was absent, a significant improvement in the sperm motility characteristics was observed only in the OTtreated samples. Conclusion: The results of this study indicate that OT at the concentration of 2 IU/ml has got a stimulatory effecton sperm motility characteristics; also, the use of SPM succeeds to supportthis effect.

References

  1. Thonneau P, Marchand S, Tallec A et al. Incidence and main causes of infertility in a resident population (1.850.000) of three French regions. Hum. Reprod. 1991;6:811-816.
  2. Acacio BD, Gottfried T, Israel R and Sokol RZ. Evaluation of a large cohort of men presenting for a screening semen analysis. Fertil. Steril.2000:73:595-597.
  3. Forti G and Krausz C. Evaluation and treatment of the infertile couple. J. Clin. Endocrinol. Metab. 1998; 83:4177-4188.
  4. Baker G, Liu DY and Boume H. Assessment of the male and preparation of sperm for ARTs. In: Trounson AO and Grander DKEditors. Handbook ofin vitro fertilization 2nded. Boca Raton. CRC Press; 1999. P.126.
  5. Rees JM, Ford WC and Hull MG. Effect of caffeine and of pentoxifylline on the motility and metabolism of human spermatozoa. J. Reprod. Fertil. 1990;90: 147-156.
  6. Krausz C, Bonaccorsi L, Maggio P et al. Andrology: Two functional assays of sperm responsiveness to progesterone and their predictive values in in vitro fertilization. Hum. Reprod. 1996; 11:1661-1667.
  7. Swaab DF.Neurobiology and Neuropathology of the Human Hypothalamus. In: BjorklundA and Hokfelt T Editors.Handbook of Chemical Neuroanatomy. The Primate nervous system. Part 1, Vol. 13. Elsevier.Amsterdam. 1997.p. 39-137.
  8. Walch K, Eder R, Schindler A and Feichtinger W. The effect of single-dose oxytocin application on time to ejaculation and seminal parameters in men. J. Assist. Repro. Genet. 2001; 18: 655-658.
  9. Byrne MM, Rolf C, Depenbusch M, Cooper TG and Nieschlag E. Lack of a single i.v. dose of oxytocin on sperm output in severely oligozoospermicmen. Hum. Reprod. 2003; 18:2098-2102.
  10. Rolf C, Behre HM, Cooper TG, Koppers B and Nieschlag E. Creatine kinase activity in human spermatozoa and seminal plasma lacks predictive value for male fertility in in vitro fertilization. Fertil. Steril. 1998; 69:727-734.
  11. World Health Organization. Reference values of semen variables. In: WHO laboratory manual for the examination of human semen and semen-cervical mucus interaction. 4th ed. Cambridge University Press,Cambridge, UK. 1999,4-33.
  12. Hinting AA. Method of semen analysis. In: Assessment of human sperm fertilizing ability. Ph.D. Thesis. University of Michigan, USA. 1989
  13. Daniel WW. Biostatistics: A Foundation for Analysis in the Health Sciences. JohnWiley and Sons, New York. 1983
  14. Alexander NJ. Male evaluation and semen analysis. Clin. Obstet. Gynecol. 1982;25:463-493.
  15. Turek PJ. Male Infertility. In: Tanagho EA and Mc Aninch JW Editors. Smith's General Urology. 15th ed. The Mc Graw- Hill Companies. USA. 2000; p.750-787.
  16. Lahdetie J. Occupation- and exposure- related studies on human sperm. J. Occup. Environ. Med. 1995;37:922-930.
  17. De Celis R, Feria-Velasco A, Gonzalez-Unzaga M, TorresCalleja J and Pedron-Nuevo N. Semen quality of workers occupationally exposed to hydrocarbons. Fertil. Steril. 2000; 73: 221-228.
  18. Shibahara H, Tsunoda T, Taneichi A, Hirona YOhno A and Takamizawa S. Diversity of antisperm antibodies bound to sperm surface in male immunologic infertility. Am. J. Reprod. Immunol.2002:47:146-150.
  19. WolffH.The biologicsignificance ofwhite blood cells in semen. Fertil. Steril. 1995; 63:1143-1157.
  20. Fuchs U, Leipnitz C and LippertT. The action of oxytocin on sperm motility. In vitro experiments with bull spermatozoa. Clin. Exp. Obstet. Gynecol. 1989; 16:95-97.
  21. Cohen J, Edward M, Fehilly C et al. In vitro fertilization a treatmentformale infertility. Fertil. Steril. 1985;43:422-432.
  22. Al-Rawi N Kh. Effects of calcium chloride and zinc chloride on sperm function in asthenospermic men in vitro. High Diploma Thesis. Baghdad University. Baghdad, Iraq. 2005
  23. Al-wakeelHA. Human sperm activation of first split ejaculate in asthenospermic and oligoasthenospermic infertile patients in Najaf. M.Sc. Thesis. Kufa University. Kufa, Iraq. 2000
  24. Tash JS, Hidaka H and Means AR. Axokinin phosphorylation by CAMP dependent protein kinase insufficient for activation of spermflagellarmotility. J. Cell. Biol. 1986; 103:649-655.
  25. Bracho GE, Fritch JJ and Tash JS. Identification of flagellar proteins that initiate the activation of sperm motility in vivo. Biochem. Biophys. Res. Commun. 1998;242:231-237.
  26. Guraya SS. Cellular and molecular biology of capacitation and acrosome reaction in spermatozoa. Int. Rev. Cytol. 2000; 199: 1- 64.
  27. Lin Y and Kan F. Regionalization and redistribution of membrane phospholipids and cholesterol in mouse spermatozoa during in vitro capacitation. Biol, Reprod. 1996;55: 1133-1146.
  28. Laverge H, DeSutter P, Desmet R, Elst J and Dhont M. Prospective randomized study comparing human serum albumin with fetal cord serum as protein supplement in culture medium for in vitro fertilization. Hum. Reprod. 1997; 12: 2263-2266.