2010
DOI: 10.1016/j.cryobiol.2010.09.001
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Effects of antioxidants on post-thawed bovine sperm and oxidative stress parameters: Antioxidants protect DNA integrity against cryodamage

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Cited by 169 publications
(111 citation statements)
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“…Total abnormalities also decreased in the presence of dithioerithritol and linoleic acid. These results were in agreement with those reported by some researchers, suggesting that antioxidants could decrease the sperm acrosome and total abnormalities for bovine [27,32,33] and for goat [26] . The sperm plasma membrane is sensible to peroxidative damage with accompanying loss of membrane integrity, reduced sperm motility, and finally loss in fertility [34] .…”
Section: Discussionsupporting
confidence: 83%
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“…Total abnormalities also decreased in the presence of dithioerithritol and linoleic acid. These results were in agreement with those reported by some researchers, suggesting that antioxidants could decrease the sperm acrosome and total abnormalities for bovine [27,32,33] and for goat [26] . The sperm plasma membrane is sensible to peroxidative damage with accompanying loss of membrane integrity, reduced sperm motility, and finally loss in fertility [34] .…”
Section: Discussionsupporting
confidence: 83%
“…In this study, by the addition of the antioxidants fetuin, dithioerithritol and linoleic acid, DNA integrity was well-kept, compared to the control group. These results were consistent to those reported in a previous research on bovine sperm [32] . On the other hand, the antioxidants which were used had no effects on upgrading at DNA integrity [27] .…”
Section: Discussionsupporting
confidence: 83%
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“…It is widely acknowledged that the cryo-and oxidative damage resulting from freezing and thawing may lead to a decline in sperm motility, viability and membrane fluidity (Ball 2008;Bucak et al 2010). Sperm cryopreservation has been repeatedly associated with axonemal alterations, leading to disruptions to sperm motion behaviour and mitochondrial membrane potential, ATP depletion, premature acrosome reaction and increased morphological alterations (de Lamirande and Gagnon 1992;Ball 2008).…”
Section: Discussionmentioning
confidence: 99%
“…The use of TCM-199, supplemented with 10% foetal bovine serum, pyruvate, follicle-stimulating hormone, estradiol, and antibiotics, remains the method used in most laboratories to culture mature bovine embryos (Sirard et al, 1988). Frozen-thawed bull semen diluted in TCM-199 supplemented with antioxidants did not show significant improvement in sperm motility characteristics (Bucak et al, 2010;Sarıözkan et al, 2014), but increased post-thaw sperm acrosome damage and abnormalities (Sarıözkan et al, 2014). To the knowledge of the authors, there is no study available, to date, on the liquid preservation of freshly collected bull semen using TCM-199 or Ham's F10 culture media.…”
Section: Introductionmentioning
confidence: 99%