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Decreasing glycerol content by co-supplementation of trehalose and taxifolin hydrate in ram semen extender: Microscopic,oxidative stress,and gene expression analyses
Institution:1. Institute for Animal Health and Cattle Development, University of León, León, Spain;2. Department of Molecular Biology, University of León, León, Spain;3. Department of Medicine, Surgery and Veterinary Anatomy, University of León, León, Spain;4. Division for Research and Post-graduate Studies, Technological Institute of Conkal, Yucatán, México;1. Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran;2. Abortion Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran;1. Centre de Recherche en Reproduction, Développement et Santé Intergénérationnelle, Département des Sciences Animales, Université Laval, Québec, QC G1V 0A6, Canada;2. Département des Sciences Animales, Université Laval, Québec, QC G1V 0A6, Canada;3. Département d''obstétrique, Gynécologie et Reproduction, Centre de Recherche en Reproduction, Développement et Santé Intergénérationnelle, Santé de la mère et de l''enfant, Centre de Recherche du CHU de Québec, QC G1V 4G2, Canada
Abstract:This study aimed to evaluate the comparative effects of taxifolin hydrate and trehalose on the quality of frozen-thawed ram spermatozoa for the first time. Ejaculates collected from six mature rams were pooled, and divided to eight equal aliquots to extend them with different concentrations of glycerol (%5 and %3), taxifolin hydrate (10, 100, and 500 μM), and trehalose (60 mM) as eight groups (G5T0, G5T10, G5T100, G5T500, G3T0, G3T10, G3T100, and G3T500). After freeze-thawing process of cryopreservation, microscopic and oxidative stress parameters, and gene expression levels were investigated for understanding of possible impacts of taxifolin hydrate and trehalose. The study showed that G3T10 resulted in the highest post-thawed viability and mitochondrial activity. Moreover, all extenders with taxifolin hydrate reduced DNA fragmentation in comparison to G5T0, but DNA damage was prevented at the highest rate in presence of G5T10. The level of LPO significantly decreased in the groups G5T500 and G3T100, and the expression levels of NQO1, GCLC, and GSTP1 genes significantly increased in the groups G5T100, G5T500, G3T10, and G3T100 compared to the group G5T0. Finally, co-supplementation of tris-based extender having 3% glycerol with 60 mM trehalose and 10 μM taxifolin hydrate in cryopreservation extender may be recommended to improve the quality of post-thawed ram spermatozoa. However, further in vivo and in vitro studies are suggested to evaluate fertility rates of frozen-thawed ram spermatozoa co-supplemented with trehalose and taxifolin hydrate.
Keywords:Ram semen  Cryopreservation  Taxifolin hydrate  Trehalose  Sperm parameters  Oxidative stress  Antioxidants  Gene expression
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