Morrell, Jane
- Department of Clinical Sciences, Swedish University of Agricultural Sciences
Research article2017Peer reviewedOpen access
Ortega Ferrusola, C.; Anel-Lopez, L.; Ortiz-Rodriguez, J. M.; Martin Munoz, P.; Alvarez, M.; de Paz, P.; Masot, J.; Redondo, E.; Balao da Silva, C.; Morrell, J. M.; Martinez, H. Rodriguez; Tapia, J. A.; Gil, M. C.; Anel, L.; Pena, F. J.
In order to gain insight of the modifications that freezing and thawing cause to the surviving population of spermatozoa, changes in the potential of the plasma membrane (Em) and intracellular Na+ content of stallion spermatozoa were investigated using flow cytometry. Moreover, caspase 3 activity was also investigated and the functionality of the Na+-K+ ATPase pump was investigated before and after freezing and thawing. Cryopreservation caused a significant (p<0.001) increase in the subpopulation of spermatozoa with depolarized sperm membranes, concomitantly with an increase (p<0.05) in intracellular Na+. These changes occurred in relation to activation of caspase 3 (p<0.001). Cryopreservation reduced the activity of the Na-K+ pump and inhibition of the Na+-K+ ATPase pump with ouabain-induced caspase 3 activation. It is concluded that inactivation of Na+-K+ ATPase occurs during cryopreservation, an inhibition that could play a role explaining the accelerated senescence of the surviving population of spermatozoa.
ATP; cryopreservation; flow cytometry; horse; Na+-K+; ATPase; sperm
Andrology
2017, Volume: 5, number: 6, pages: 1174-1182
Clinical Science
DOI: https://doi.org/10.1111/andr.12419
https://res.slu.se/id/publ/92380