Department of Reproduction and Artificial Insemination and Faculty of Veterinary Medicine, Fırat University, Elazığ, Turkey.
Department of Physiology, Faculty of Veterinary Medicine, Fırat University, Elazığ, Turkey.
Biopreserv Biobank. 2022 Aug;20(4):340-347. doi: 10.1089/bio.2021.0001. Epub 2021 Sep 20.
The aim of this study was to evaluate the effect of hydrated carbon 60 fullerene (CHyFn) on ram semen quality during cryopreservation. Three ejaculates from each of seven Akkaraman rams were collected using an artificial vagina during the nonbreeding season and pooled. Pooled semen samples were divided into 10 equal parts and diluted with tris + egg yolk extender not containing (control) and containing 100, 200, 400, and 800 nM and 1, 5, 10, 20, and 40 μM CHyFn at 37°C. After addition of 5% glycerol and an equilibration process for 3 hours, the samples were frozen in 0.25-mL straws in an automatic freezing device at -140°C and stored in a liquid nitrogen container. Straws were thawed 24 hours after freezing and analyzed immediately with no incubation period. Motility, kinematic parameters, abnormality, vitality, hypo-osmotic swelling test (HOST), and oxidative stress levels were analyzed in thawed semen. Compared with the control, 200, 400, and 800 nM and 1 and 5 μM CHyFn doses increased motility and HOST values and decreased the dead sperm rate. When compared with the control, addition of CHyFn significantly decreased malondialdehyde levels (between 200 nM and 40 μM doses) and significantly increased glutathione peroxidase (between 800 nM and 40 μM doses) and catalase (between 1 and 40 μM doses) activities. In conclusion, results of this study show that the CHyFn nanoparticles are nontoxic to ram semen and their supplementation in the extender is beneficial to sperm motility and membrane integrity after freeze-thawing.
本研究旨在评估水合碳 60 富勒烯(CHyFn)对冷冻保存过程中公羊精液质量的影响。在非繁殖季节,使用人工阴道从 7 只 Akkaraman 公羊中采集每只公羊的 3 份精液,并将其混合。混合精液样本被分为 10 等份,用 tris+卵黄稀释液(不含对照)和含 100、200、400、800 nM 和 1、5、10、20、40 μM CHyFn 的稀释液在 37°C 下稀释。添加 5%甘油并在 3 小时内进行平衡过程后,将样品在 -140°C 的自动冷冻装置中以 0.25-mL straw 冷冻,并在液氮容器中储存。冷冻后 24 小时解冻 straw,并立即进行分析,无孵育期。解冻后分析精液的运动性、运动学参数、异常、活力、低渗肿胀试验(HOST)和氧化应激水平。与对照组相比,200、400、800 nM 和 1、5 μM CHyFn 剂量增加了运动性和 HOST 值,降低了死精子率。与对照组相比,添加 CHyFn 显著降低了丙二醛水平(在 200 nM 和 40 μM 剂量之间),显著增加了谷胱甘肽过氧化物酶(在 800 nM 和 40 μM 剂量之间)和过氧化氢酶(在 1 和 40 μM 剂量之间)的活性。综上所述,本研究结果表明,CHyFn 纳米颗粒对公羊精液无毒,其在稀释液中的添加有利于冻融后精子的运动性和膜完整性。