DOI QR코드

DOI QR Code

Comparison of Motility, Acrosome, Viability and ATP of Boar Sperm with or without Cold Shock Resistance in Liquid Semen at 17℃ and 4℃, and Frozen-thawed Semen

  • Yi, Y.J. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Li, Z.H. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Kim, E.S. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Song, E.S. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Kim, H.B. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Cong, P.Q. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Lee, J.M. (Research Center for Transgenic Cloned Pigs, Chungnam National University) ;
  • Park, Chang-Sik (Research Center for Transgenic Cloned Pigs, Chungnam National University)
  • Received : 2007.06.22
  • Accepted : 2007.09.03
  • Published : 2008.02.01

Abstract

This study was designed to analyze boar sperm to compare motility, acrosome morphology, viability and ATP by various preservation methods between Duroc boar A with cold shock resistance sperm and Duroc boar B with cold shock sensitivity sperm. Semen volume, sperm concentration, motility and normal acrosome between Duroc boar A and B did not show any differences within 2 h after collection. There were no differences in sperm motility and normal acrosome between boar A and B at 1 day of preservation at $17^{\circ}C$ and $4^{\circ}C$, respectively. However, sperm motility and normal acrosome from 2 day of preservation at $17^{\circ}C$ and $4^{\circ}C$, respectively, were higher for boar A than boar B. The frozen-thawed sperm motility and normal acrosome were higher for boar A than boar B. The sperm viability and ATP concentration according to storage period of liquid semen at $17^{\circ}C$ and $4^{\circ}C$ were higher for boar A than boar B. Also, the sperm viability and ATP concentration of frozen-thawed semen were higher for boar A than boar B. In conclusion, we found out that the original quality of boar semen with cold shock resistance sperm played an important role.

Keywords

References

  1. Aalbers, G. J., L. A. Johnson, E. A. Aalbers-Smit and J. H. M. Rademaker. 1985. ATP content of fresh and frozen-thawed boar semen and its relationship to sperm concentration and fertility. In: Deep freezing of boar semen (Ed. L. A. Johnson and K. Larsson), Swedish University of Agricultural Science, Uppsala, pp. 259-264.
  2. Andersen, K. 1974. Morphological abonormalities in the acrosome and nucleus of boar spermatozoa. Nord. Vet. Med. 26:215-218.
  3. Bane, A. 1961. Acrosomal abnormality associated with sterility in boar. In: IVth International Congress of Animal Reproduction, Hague, The Netherlands, 4:810-817.
  4. Bredderman, P. J. and R. H. Foote. 1971. Factors stabilizing bull sperm cell volume and prolonging motility at high dilution. Exp. Cell Res. 66:458-464. https://doi.org/10.1016/0014-4827(71)90701-4
  5. De Ambrogi, M., J. Ballester, F. Saravia, I. Caballero, A. Johannisson, M. Wallgren, M. Andersson and H. Rodriguez-Martinez. 2006. Effect of storage in short- and long-term commercial semen extenders on the motility, plasma membrane and chromatin integrity of boar spermatozoa. Int. J. Androl. 29(5):543-552. https://doi.org/10.1111/j.1365-2605.2006.00694.x
  6. Fawcett, D. W. 1975. The mammalian spermatozoon. Dev. Biol. 44:394-436. https://doi.org/10.1016/0012-1606(75)90411-X
  7. Ford, S. R. and F. R. Leach. 1998. Bioluminescent assay of the adenylate energy charge. Methods Mol. Biol. 102:69-81.
  8. Foulkes, J. A. and B. J. MacDonald. 1979. The relationship between ATP content and motility of bovine spermatozoa. Theriogenol. 11:313-319. https://doi.org/10.1016/0093-691X(79)90073-6
  9. Garner, D. L., L. A. Johnson, S. T. Yue, B. L. Roth and R. P. Haugland. 1994. Dual DNA staining assessment of bovine sperm viability using SYBR-14 and propidium iodide. J. Androl. 16:620-629.
  10. Garner, D. L. and L. A. Johnson. 1995. Viability assessment of mammalian sperm using SYBR-14 and propidium iodide. Biol. Reprod. 53:276-284. https://doi.org/10.1095/biolreprod53.2.276
  11. Guminska, M., T. Kedryna, A. Laszcska, M. Godlewski and B. Szczesniak-Fabianczyk. 1997. Changes in ATP level and iron-induced ultra-weak photon emission in bull spermatozoa, caused by membrane peroxidation during thermal stress. Acta Biochim. Pol. 44:131-138.
  12. Jeulin, C. and J-C. Soufir. 1992. Reversible intracellular ATP changes in intact rat spermatozoa and effects on flagellar sperm movement. Cell Motil. Cytoskeleton 21:201-222.
  13. Johnson, L. A., J. G. Aalbers, C. M. T. Willems and W. Sybesma. 1981. Use of boar spermatozoa for artificial insemination. I. Fertilizing capacity of fresh and frozen spermatozoa in sows on 36 farms. J. Anim. Sci. 52:1130-1136. https://doi.org/10.2527/jas1981.5251130x
  14. Johnson, L. A., K. F. Weitze, P. Fiser and W. M. C. Maxwell. 2000. Storage of boar semen. Anim. Reprod. Sci. 62:143-172. https://doi.org/10.1016/S0378-4320(00)00157-3
  15. Kahn, W. 1981. Zur ATP- und AMP-Bestimmung mit dem Biolumineszenzverfahren im Sperma einiger Haustiere und des Menschen. Vet. Med. Diss. Munchen.
  16. Krider, J. L., J. H. Conrad and W. E. Carroll. 1982. Swine Production. New York: McGraw-Hill Publications, pp. 179-182.
  17. Mendeluk, G. R., M. J. Munuce, C. Carizza, M. Sardi and C. Bregni. 1997. Sperm motility and ATP content in seminal byperviscosity. Arch Androl. 39:223-227. https://doi.org/10.3109/01485019708987920
  18. Mujica, A., L. Neri-Bazan, J. S. Tash and S. Uribe. 1994. Mechanism for procaine mediated hyperactivated motility in guinea pig spermatozoa. Mol. Reprod. Dev. 38:285-292. https://doi.org/10.1002/mrd.1080380309
  19. Oh, S. H., M. T. See, T. E. Long and J. M. Galvin. 2006. Estimates of genetic correlations between production and semen traits in boar. Asian-Aust. J. Anim. Sci. 19(2):160-164.
  20. Park, C. S., M. Y. Kim, Y. J. Yi, Y. J. Chang, S. H. Lee, J. J. Lee, M. C. Kim and D. I. Jin. 2004. Liquid boar sperm quality during storage, and in vitro fertilization and culture of pig oocytes. Asian-Aust. J. Anim. Sci. 17(10):1369-1373. https://doi.org/10.5713/ajas.2004.1369
  21. Paquignon, M., J. Bussiere, F. Bariteau and M. Courot. 1980. Effectiveness of frozen boar semen under practical conditions of artificial insemination. Theriogenol. 14:217-226. https://doi.org/10.1016/0093-691X(80)90006-0
  22. Phillips, D. M. 1977. Mitochondrial disposition in mammalian spermatozoa. J. Ultrastruct. Res. 2:144-154.
  23. Pursel, V. G. and L. A. Johnson. 1971. Procedure for the preservation of boar spermatozoa by freezing. US Dept. Agric. ARS, pp. 44-227.
  24. Pursel, V. G., L. A. Johnson and G. B. Rampacek. 1972a. Acrosome morphology of boar spermatozoa incubated before cold shock. J. Anim. Sci. 34:278-283. https://doi.org/10.2527/jas1972.342278x
  25. Pursel, V. G., L. A. Johnson and L. L. Schulman. 1972b. Loss of boar sperm fertilizing capacity associated with altered acrosome morphology during in vitro storage. In: VIIth International Congress Animal Reproduction and AI, Munich, Germany, II, pp. 1525-1600.
  26. Pursel, V. G. and L. A. Johnson. 1975. Freezing of boar spermatozoa: fertilizing capacity with concentrated semen and a new thawing procedure. J. Anim. Sci. 40:99-102. https://doi.org/10.2527/jas1975.40199x
  27. Pursel, V. G. and C. S. Park. 1985. Freezing and thawing procedures for boar spermatozoa. In: (Ed. L. A. Johnson and K. Lasson), Deep Freezing of Boar Semen. Uppsala, Sweden, Swedish University of Agricultural Science, pp. 147-166.
  28. Schuler, D., U. Kupfer and F. Zimmerman. 1979. Deep freezing of boar semen: A comparison of two freezing methods. Schweiz Arch Tierheilk 121:173-178.
  29. Velez Cuevas, G. 1982. Untersuchungen uber die Eignung des ATP- ADP- und AMP-Nachweises mit der Biolumineszenz-methode zur Bullen-spermien. Vet. Med. Diss. Munchen.
  30. Westendorf, P., L. Richter and H. Treu. 1975. Zur Tiefgerierung von Ebersperma Labor- und Besamungsergebnisse mit dem Husenberger Pailletten-Verfahren. Dtsch. Tierarztl. Wschr. 82:261-300.
  31. Yi, Y. J., Y. A. Kwon, H. J. Ko and C. S. Park. 2002. Effects of diluent component, freezing rate, thawing time and thawing temperature on acrosome morphology and motility of frozen-thawed boar sperm. Asian-Aust. J. Anim. Sci. 15(11):1553-1558. https://doi.org/10.5713/ajas.2002.1553

Cited by

  1. Energy metabolic state in hypothermically stored boar spermatozoa using a revised protocol for efficient ATP extraction vol.5, pp.11, 2016, https://doi.org/10.1242/bio.017954
  2. Relationship between post-thaw adenosine triphosphate content, motility and viability in cryopreserved bovine semen applying two different preservation methods pp.09366768, 2018, https://doi.org/10.1111/rda.13285
  3. Comparison of Viability, ATP and In vitro Fertilization of Boar Sperm Stored at 4℃ in the Three Different Diluents vol.21, pp.8, 2008, https://doi.org/10.5713/ajas.2008.80055