Czech J. Anim. Sci., 2006, 51(2):61-65 | DOI: 10.17221/3910-CJAS

Effect of long-term storage on induced photon emission of boar spermatozoa

P. Gogol, B. Szczęśniak-Fabiańczyk
Department of Biotechnology of Animal Reproduction, National Research Institute of Animal Production, Balice/Kraków, Poland

Ultraweak photon emission measurements were found to be a useful tool for investigating the influence of stress factors on cells. In the present study, induced photon emission of boar spermatozoa was investigated using a luminometer during a 12-day storage at 15°C in Biosolwens extender. It was shown that the day of storage had a significant effect on some photon emission parameters. During storage, a significant increase in the Integral, Peak max. and Slope max. parameters and a decline in the T.-half (fall) parameter were observed. A significant correlation was observed between photon emission parameters and sperm motility. In conclusion, the results of the present study indicate that the measurement of induced photon emission can be an alternative, sensitive and relatively simple method for assessing the effect of preservation on oxidative damage to boar spermatozoa.

Keywords: boar semen; oxidative stress; luminescence; photon emission; sperm motility

Published: February 28, 2006  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Gogol P, Szczęśniak-Fabiańczyk B. Effect of long-term storage on induced photon emission of boar spermatozoa. Czech J. Anim. Sci. 2006;51(2):61-65. doi: 10.17221/3910-CJAS.
Download citation

References

  1. Aitken R.J., Clarkson J.S., Fisher S. (1989): Generation of reactive oxygen species, lipid peroxidation and human sperm function. Biol. Reprod., 41, 183-197. Go to original source... Go to PubMed...
  2. Aitken R.J., Harkiss D., Buckingham D.W. (1993a): Relationship between iron-catalysed lipid peroxidation potential and human sperm function. J. Reprod. Fertil., 98, 257-265. Go to original source... Go to PubMed...
  3. Aitken R.J., Harkiss D., Buckingham D.W. (1993b): Analysis of lipid peroxidation mechanisms in human spermatozoa. Mol. Reprod. Dev., 35, 302-315. Go to original source... Go to PubMed...
  4. Aitken R.J., Paterson M., Fisher H., Buckingham D.W., van Duin M. (1995): Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J. Cell Sci., 108, 2017-2025. Go to original source... Go to PubMed...
  5. Aitken R.J., Gordon E., Harkiss D., Twigg J.P., Milne P., Jennings Z., Irvine D.S. (1998): On the relative impact of oxidative stress on the functional competence and genomic integrity of human spermatozoa. Biol. Reprod., 59, 1037-1046. Go to original source... Go to PubMed...
  6. Albertini R., Abuja P.M. (1998): Monitoring of low-density lipoprotein oxidation by low - level chemiluminescence. Free Radic. Res., 29, 75-83. Go to original source... Go to PubMed...
  7. Armstrong J.S., Rajasekaran M., Chamulitrat W., Gatti P., Hellstrom W.J., Sikka S.C. (1999): Characterization of reactive oxygen species induced effects on human spermatozoa movement and energy metabolism. Free Radic. Biol. Med., 26, 869-880. Go to original source... Go to PubMed...
  8. Boveris A., Cadenas E., Reiter R., Filipkowski M., Nakase Y., Chance B. (1980): Organ chemiluminescence: noninvasive assay for oxidative radical reactions. Proc. Natl. Acad. Sci. U.S.A., 77, 347-51. Go to original source... Go to PubMed...
  9. Cecil H.C., Bakst M.R. (1993): In vitro lipid peroxidation of turkey spermatozoa. Poult. Sci., 72, 1370-1378. Go to original source...
  10. Cerolini S., Maldjian A., Surai P., Noble R. (2000): Viability, susceptibility to peroxidation and fatty acid composition of boar semen during liquid storage. Anim. Reprod. Sci., 58, 99-111. Go to original source... Go to PubMed...
  11. Comporti M. (1989): Three models of free radical-induced cell injury. Chem. Biol. Interact., 72, 1-56. Go to original source... Go to PubMed...
  12. De Lamiranda E., Gagnon C. (1992): Reactive oxygen species and human spermatozoa. II. Depletion of adenosine triphosphate plays an important role in the inhibition of sperm motility. J. Androl., 13, 379-386. Go to original source... Go to PubMed...
  13. Doi H., Iwasaki H., Masubuchi Y., Nishigaki R., Horie T. (2002): Chemiluminescence associated with the oxidative metabolism of salicylic acid in rat liver microsomes. Chem. Biol. Interact., 140, 109-119. Go to original source... Go to PubMed...
  14. Donnelly E.T., McClure N., Lewis S.E. (1999): The effect of ascorbate and alpha-tocopherol supplementation in vitro on DNA integrity and hydrogen peroxide-induced DNA damage in human spermatozoa. Mutagenesis, 14, 505-512. Go to original source... Go to PubMed...
  15. Gogol P. (2005): Iron-induced luminescence of boar spermatozoa cells. Ann. Anim. Sci., 5, 12-17.
  16. Gonzalez-Flecha B., Llesuy S., Boveris A. (1991): Hydroperoxide-initiated chemiluminescence: an assay for oxidative stress in biopsies of heart, liver, and muscle. Free Radic. Biol. Med., 10, 93-100. Go to original source... Go to PubMed...
  17. Hammerstedt R.H. (1993): Maintenance of bioenergetic balance in sperm and prevention of lipid peroxidation: review of the effect on design of storage preservation systems. Reprod. Fertil., 5, 675-690. Go to original source... Go to PubMed...
  18. Hammerstedt R.H. (1996): Evaluation of sperm quality: Identification of the subfertile male and courses of action. Anim. Reprod. Sci., 24, 77-87. Go to original source...
  19. Holt C., Holt W.V., Moore H.D.M., Reed H.C.B., Curnock R.M. (1997): Objectively measured boar sperm motility parameters correlate with the outcomes of on-farm inseminations: results of two fertility trials. J. Androl., 18, 312-323. Go to original source... Go to PubMed...
  20. Kobayashi T., Miyazaki T., Natori M., Nozawa S. (1991): Protective role of superoxide dismutase in human sperm motility: superoxide dismutase activity and lipid peroxide in human seminal plasma and spermatozoa. Hum. Reprod., 6, 987-991. Go to original source... Go to PubMed...
  21. Laszczka A., Godlewski M., Kwiecińska T., Rajfur Z., Sitko D., Szczęśniak-Fabiańczyk B., Sławiński J. (1995): Ultraweak luminescence of spermatozoa. Curr. Top. Biophys., 19, 20-21.
  22. Mammoto A., Masumoto N., Tahara M., Ikebuchi Y., Ohmichi M., Tasaka K., Miyake A. (1996): Reactive oxygen species block sperm-egg fusion via oxidation of sperm sulfhydryl proteins in mice. Biol. Reprod., 55, 1063-1068. Go to original source... Go to PubMed...
  23. Marshall P.J., Warso M.A., Lands W.E.M. (1985): Selective microdetermination of lipid hydroperoxides. Anal. Biochem., 145, 192-199. Go to original source... Go to PubMed...
  24. Miyazawa T., Fujimoto K., Kinoshita M., Usuki R. (1994): Rapid estimation of peroxide content of soybean oil by measuring thermoluminescence. J. Am. Oil Chem. Soc., 71, 343-345. Go to original source...
  25. Ohta A., Mohri T., Ohyashiki T. (1989): Effect of lipid peroxidation on membrane-bound Ca2+-ATPase activity of the intestinal brush-border membranes. Biochem. Biophys. Acta, 984, 151-157. Go to original source... Go to PubMed...
  26. Selley M.L., Lacey M.J., Bartlett M.R., Copeland C.M., Ardlie N.G. (1991): Content of significant amounts of a cytotoxic end-product of lipid peroxidation in human semen. J. Reprod. Fertil., 92, 291-298. Go to original source... Go to PubMed...
  27. Sławiński J., Ezzahir A., Godlewski M., Kwicińska T., Rajfur Z., Sitko D., Wierzuchowska D. (1992): Stress-induced photon emission from perturbed organisms. Experientia, 48, 1041-1058. Go to original source... Go to PubMed...
  28. Sławiński J., Godlewski M., Gumińska M., Kędryna T., Kwiecińska T., Laszczka A., Szczęśniak-Fabiańczyk B., Wierzuchowska D. (1998): Stress-induced peroxidation and ultraweak photon emission of spermatozoa cells. Curr. Top. Biophys., 22, 195-203.
  29. Tardif S., Laforest J.P., Cormier N., Bailey J.L. (1999): The importance of porcine sperm parameters on fertility in vivo. Theriogenology, 52, 447-459. Go to original source... Go to PubMed...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.