Warianty tytułu
Języki publikacji
Abstrakty
In this study, different assays were used to assess the structural and functional integrity of the sperm plasma membrane following freezing-thawing of the whole ejaculates (WEs) and sperm-rich fractions (SRFs) of boar semen. Besides sperm viability assessments (motility and mitochondrial membrane potential using a mitochondrial specific dye, JC-1 with propidium iodide, PI), sperm plasma membrane integrity (PMI) assessments were determined simultaneously using different membrane-based tests (SYBR- 14/PI and carboxyfluorescein diacetate (CFDA) with PI (CFDA/PI), and the hypo-osmotic swelling (HOS) test). ANOVA results showed that boar variability had a significant effect on the analysed parameters of post-thaw sperm characteristics. Spermatozoa harvested from the WEs exhibited a marked decline in post-thaw viability, manifested in reduced motility and mitochondrial membrane potential, than those originated from the SRFs after freezing-thawing. Cryopreservation compromised sperm PMI, as indicated in a significant decline in SYBR-stained, CFDA-stained or HOS-positive sperm cells, irrespective of the ejaculate collection procedure. It was observed that the membrane-based tests were strongly inter-correlated. Furthermore, agreement between the measurements of the membrane-based tests was confirmed by the Bland-Altman scatter plots of differences, suggesting that these tests could detect the same sperm cohorts, which were susceptible to cryo-induced membrane damage. The findings of this study indicate that dual fluorescent staining with SYBR-14/PI and CFDA/PI assays, in combination with the HOS test, provide more precise description of the sperm populations in frozen-thawed boar semen.
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Opis fizyczny
p.231-236,fig.,ref.
Twórcy
autor
- Department of Animal Biochemistry and Biotechnology, Faculty of Animal Bioengineering, Warmia and Mazury University in Olsztyn, Poland
autor
autor
autor
Bibliografia
- 1. Bland J.M., Altman D.G.: Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986,1(8476), 307-310.
- 2. Buhr M.M., Curtis E.F., Somnapan Kakuda N.: Composition and behaviour of head membrane lipids of fresh and cryopreserved boar sperm. Cryobiology 1994, 31, 224-238.
- 3. Dziekońska A., Fraser L., Strzeżek J.: Effect of different storage temperatures on the metabolic activity of spermatozoa following liquid storage of boar semen. J Anim Feed Sci 2009, 18, 638-649.
- 4. Fraser L., Lecewicz M., Strzeżek J.: Fluorometric assessments of viability and mitochondrial status of boar spermatozoa following liquid storage. Pol J Vet Sci 2002, 5, 85-92.
- 5. Fraser L., Strzeżek J.: Effect of different procedures of ejaculate collection, extenders and packages on DNA integrity of boar spermatozoa following freezing- thawing. Anim Reprod Sci 2007, 99, 317-329.
- 6. Garner D.L., Johnson L.A.: Viability assessment of mammalian sperm using SYBR-14 and propidium iodide. Biol Reprod 1995, 53, 276-284.
- 7. Gączarzewicz D., Piasecka M., Udała J., Błaszczyk B., Stankiewicz T., Laszczyńska M.: Plasma membrane changes during the liquid storage of boar spermatozoa: a comparison of methods. Acta Vet Hung 2010, 58, 105- 116.
- 8. Jeyendran R.S., van der Ven H.H., Perez-Pelaez M., Crabo B.G., Zaneveld L.J.D.: Development of an assay to assess the functional integrity of the human sperm plasma membrane and its relationship to other semen characteristics. J Reprod Fertil 1984, 70, 219-228.
- 9. Johnson L.A., Weitze K.F., Fiser P., Maxwell W.M.: Storage of boar semen. Anim Reprod Sci 2000, 62, 143- 172.
- 10. Juonala T., Salonen E., Nurttila T., Anderson M.: Three fluorescence methods for assessing boar sperm viability. Reprod Dom Anim 1999, 34, 83-87.
- 11. Kordan W., Lecewicz M., Tobolski J.: Effect of platelet activating factor on motility, plasmalemma integrity, the process of capacitation and acrosome reaction of fresh and cryopreserved boar spermatozoa. Pol J Vet Sci 2009, 12, 175-181.
- 12. Moce E., Graham J. K.: In vitro evaluation of sperm quality. Anim Reprod Sci 2008, 105, 104-118.
- 13. Parks J.E., Lynch D.V.: Lipid composition and thermotropic phase behavior of boar, bull, stallion, and rooster sperm membranes. Cryobiology 1992, 29, 255- 266.
- 14. Peña F.J.: Detecting subtle changes in sperm membranes in veterinary andrology. Asian J Androl 2007, 9, 731- 737.
- 15. Strzeżek J., Glogowski J., Hopfer E., Wojtkiewicz K.: The "Kortowska" method of freezing boar semen. Medycyna Wet 1985, 41, 349-353.
- 16. Strzeżek J., Lecewicz L., Dziekońska A., Fraser L.: A simple method of extraction of lipoprotein fractions from avian egg yolk - protective effect on cooled boar semen. Theriogenology 2005, 63, 496-497.
- 17. Sutkeviciene N., Riskeviciene V., Januskauskas A., Zilinskas H., Andersson M.: Assessment of sperm quality traits in relation to fertility in boar semen. Acta Vet Scand 2009, 51, 53; doi: 10. 1186/1751 -0147-51 -53.
- 18. Thurston L.M., Siggins K., Mileham A.J., Watson P.F., Holt W.V.: Identification of amplified restriction fragment length polymorphism markers linked to genes controlling boar sperm viability following cryopreservation. Biol Reprod 2002, 66, 545-554.
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Bibliografia
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