M.
Carmen Vílchez, Marina Morini, David S. Peñaranda, Víctor Gallego, Juan F.
Asturiano, Luz Pérez
Abstract
The role of seminal
plasma sodium and activation media sodium on sperm motility was examined by
selectively removing the element from these two media, in European eel sperm.
Sperm size (sperm head area) was also measured using an ASMA (Automated Sperm
Morphometry Analyses) system, in the different conditions. Intracellular sodium
[Na+]i was quantitatively analyzed by first time in the spermatozoa from a
marine fish species. Measurement of [Na+]i was done before and after motility
activation, by Flow Cytometry, using CoroNa Green AM as a dye. Sperm motility
activation induced an increase in [Na+]i, from 96.72 mM in quiescent stage to
152.21 mM post-activation in seawater. A significant decrease in sperm head
area was observed post-activation in seawater. There was a notable reduction in
sperm motility when sodium was removed from the seminal plasma, but not when it
was removed from the activation media. Sodium removal was also linked to a
significant reduction in sperm head area in comparison to the controls. Our
results indicate that the presence of the ion Na+ in the seminal plasma (or in
the extender medium) is necessary for the preservation of sperm motility in
European eel, probably because it plays a role in maintaining an appropriate
sperm cell volume in the quiescent stage of the spermatozoa.
No hay comentarios:
Publicar un comentario
Nota: solo los miembros de este blog pueden publicar comentarios.