Cold storage of sperm of rainbow trout (Oncorhynchus mykiss): Effect on motility, intracellular superoxide, plasma membrane integrity and mitochondrial membrane potential

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datacite.alternateIdentifier.citationARCHIVOS DE MEDICINA VETERINARIA,Vol.42,179-186,2010
datacite.alternateIdentifier.doi10.4067/S0301-732X2010000300009
datacite.creatorBerrios, O.
datacite.creatorValdebenito Isler, Iván
datacite.creatorTreulen, F.
datacite.creatorUbilla Madrid, Andrea
datacite.date2010
datacite.subject.englishstorage
datacite.subject.englishintracellular superoxide
datacite.subject.englishrainbow trout
datacite.subject.englishspermatozoa
datacite.titleCold storage of sperm of rainbow trout (Oncorhynchus mykiss): Effect on motility, intracellular superoxide, plasma membrane integrity and mitochondrial membrane potential
dc.date.accessioned2021-04-30T16:25:27Z
dc.date.available2021-04-30T16:25:27Z
dc.description.abstractIn teleostei, as opposed to what happens in mammals, most of the studies that evaluate the quality storages of semen are oriented toward the exposure of spermatozoa to some reactive oxygen species (ROS), the utilization of antioxidants in the diet, or the incorporation of these in seminal plasma. There is no available the literature covering the presence of superoxide ions (O-2(center dot-)), or the function of these on the interior of the spermatozoa that have been stored. In this study. we evaluated the effect of storage on intracellular O-2(center dot-) motility, plasmatic membrane integrity, and mitochondrial membrane potential (Delta Psi(Mit)) of spermatozoa of rainbow trout (Oncorhynchus mykiss). Semen was extracted and put into storage for 12 days at 4 degrees C. Spermatozoa motility, (Delta Psi(Mit)) plasmatic membrane integrity were evaluated every 4 days, and intracellular O-2(center dot-), was detected. It was found that 82.59% of the cells were positive for the staining of O-2(center dot-) on the day of sample extraction, while sperm motility, Delta Psi(Mit) and plasmatic membrane integrity only showed deterioration after the eighth day of storage. Only Delta Psi(Mit) is correlated negatively with O-2(center dot-) starting from the eighth day of storage (r = -0.56 P < 0.05). Regarding motility and plasmatic membrane integrity, these were not affected by intracellular O-2(center dot-), although the deterioration observed in these last two indicators, could have been caused by the prolonged contact of the spermatozoa with contaminating agents that were not evaluated in this study.
dc.identifier.urihttp://repositoriodigital.uct.cl/handle/10925/2553
dc.language.isoes
dc.publisherUNIV AUSTRAL CHILE. FAC CIENCIAS VETERINARIAS
dc.sourceARCHIVOS DE MEDICINA VETERINARIA
oaire.resourceTypeArticle
uct.catalogadorWOS
uct.indizacionSCI
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