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Effects of oxidized glutathione, bovine serum albumin, cysteine and lycopene on the quality of frozen-thawed ram semen
Acta Veterinaria Brno Cilt 76 ss. 383-390
Scopus Open Access Toplam 198 atıf DOI
Free radicals are known to be involved in lipid peroxidation as well as DNA and sperm membrane damages that may lead to decreased sperm motility or cell death. The balance between free radical production and their detoxification may be an important factor in sperm survival and function before, during and after cryopreservation. The aim of this study was to determine the effects of the addition of the antioxidants of oxidized glutathione (GSSG), bovine serum albumin (BSA), cysteine and lycopene to freezing media on the post-thawing sperm characteristics, including motility, morphology, acrosome integrity, viability and membrane integrity. A total number of 42 ejaculates were collected using the artificial vagina from 4 Akkaraman rams and 10 replicates of the ejaculates were diluted with a Tris-based extender containing additives and no additives as control. GSSG (5 mM), BSA (20 mg/ml), cysteine (10 mM) and lycopene (800 μg) showed more positive effects than other concentrations of the supplements and controls in protecting sperm characteristics after the freezing-thawing process (P < 0.001). Many aspects of sperm protection, e.g. sperm motility, viability and membrane stabilisation of the sperm cells during relative cryopreservation, are the key factors in determining the preservation of sperm function. The results of this study provide a new approach to the cryopreservation of sperm from rams and related breeds, and thereby contribute to the improvement of these breeds for the world sheep industry.
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Antioxidant supplementation ameliorates bull sperm parameters and fertilizing ability following the freeze-thaw process
Turkish Journal of Veterinary and Animal Sciences Cilt 45 ss. 457-462
Scopus Havuzumuzda Open Access 8 atıf almış
This study’s goal was to reveal the effects of antioxidant supplementation on motility, motion characters, morphology, DNA integrity, and fertilizing potential of cryopreserved bovine sperm. The ejaculates were collected from three Holstein bulls. At least ten ejaculates were collected per bull. The ejaculates were immediately separated into five aliquots, diluted in the Cryobos (Magapor Co. Ltd., Zaragoza, Spain) commercial extender, including 2.5 mM taurine, 2.5 mM cysteine, 2.5 mM methionine, 2.5 mM glutamine, and no additives were used. Afterward, they were frozen in 0.25 mL French straws, and liquid nitrogen was used for the storage of semen. The supplementation of methionine resulted in a higher subjective motility rate in comparison with the other groups. Taurine led to the lowest post-thawed CASA motility rate (p < 0.05). The addition of antioxidants did not cause any improvements in sperm motion characteristics when compared to the controls (p > 0.05). Cysteine led to a higher protection of acrosome abnormality, in comparison with the other groups (p < 0.05). For the comet test, the minimum percentage of sperm with damaged DNA was obtained in the groups with cysteine and glutamine (p < 0.05). There was not any significant difference among the groups in terms of pregnancy rates (p > 0.05). In conclusion, cysteine supplementation to the semen extender prior to freezing ameliorated the post-thawed semen quality.
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Kurumlar (3)
Erciyes Üniversitesi Kayseri, Turkey
Mersin Üniversitesi Mersin, Turkey
Selçuk Üniversitesi Selçuklu, Turkey