Effects of vitamin C, vitamin E, selenium, zinc, or their nanoparticles on camel epididymal spermatozoa stored at 4 °C

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作者
Mohamed A. Shahin
Wael A. Khalil
Islam M. Saadeldin
Ayman A. Swelum
Mostafa A. El-Harairy
机构
[1] Mansoura University,Department of Animal Production, Faculty of Agriculture
[2] Mansoura University,Electron Microscope Unit
[3] King Saud University,Department of Animal Production, College of Food and Agricultural Sciences
[4] Zagazig University,Department of Physiology, Faculty of Veterinary Medicine
[5] King Faisal Specialist Hospital & Research Centre,Department of Comparative Medicine
[6] Zagazig University,Department of Theriogenology, Faculty of Veterinary Medicine
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关键词
Camel; Spermatozoa preservation; SHOTOR diluent; Antioxidants;
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摘要
This study determined the effects of antioxidant supplementation and storage time at cool temperatures on the characteristics of epididymal camel spermatozoa. Camel testes were collected at the abattoir after animal slaughtering and kept at 4 °C during transportation and until processing (max 6 h). Spermatozoa were retrieved and diluted with SHOTOR extender, split in aliquots, supplemented with the following antioxidants: 200 μm/mL vitamin E, 1.0 g/L vitamin C, 1 μg/mL selenium nanoparticles, 50 μg/mL zinc nanoparticles, 2 μg/mL sodium selenite, and 100 μg/mL zinc sulfate, and stored at 4 °C for 2, 48, 96, and 144 h. The storage time significantly affected (P < 0.05) the sperms’ motility and livability, the sperms’ membrane integrity, and the percentages of cytoplasmic droplets as well as the percentage of morphologically normal spermatozoa. Epididymal sperm characteristics (progressive motility, livability, membrane integrity, and abnormalities) were significantly improved (P < 0.05) when the spermatozoa were diluted with antioxidants as compared with the control group, and the best additives were identified as nano-selenium, sodium selenite, nano-zinc, and zinc sulfate. In conclusion, adding nano-sized minerals or inorganic trace elements and vitamins maintained the progressive motility, livability, and membrane integrity, and decreased abnormalities and cytoplasmic droplet percentages of epididymal camel spermatozoa stored at 4 °C up to 144 h.
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