Effect of captivity and cryopreservation on ROS production
DG Valcarce, V Robles
Reactive oxygen species have a great impact on spermatozoa function. Gametes from sole males born in captivity (F1) display
lower quality than those from wild individuals. In this paper, the percentage of cells positive for dichlorofluorescein (DCF+) was
determined by flow cytometry in wild and F1 animals, the effect of cryopreservation on DCF+ cells was evaluated in both groups
and the distribution of H2O2 within the cell was studied by confocal microscopy. Our results indicated that there are no
differences in either viability or DCF+ cells between wild and F1 animals when fresh samples were evaluated. However, when data
were analyzed considering two different sperm populations in terms of motility, a significant decrease in viability and DCF+ cells
was reported in low-motile F1 spermatozoa. Cryopreservation did not alter the viability or the presence of DCF+ cells in sperm
samples from wild animals, but significantly decreased the viability in F1 samples. Distribution patterns of H2O2 have been
established by confocal microscopy in Solea senegalensis spermatozoa: co-localization of H2O2 with active mitochondria
(MitoTracker+) and co-localization with nuclear DNA (DAPI). Compared with H2O2 distribution in other marine species such as
Scophthalmus maximus, Solea senegalensis spermatozoa showed widespread presence of H2O2 particularly in the nuclei, which
could potentially compromise DNA integrity.
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