Department of Zoology, Division of Science and Technology, University of Education, College Road, Township, Lahore, 54000, Pakistan.
Department of Wildlife Management, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, 46300, Pakistan.
Theriogenology. 2021 Sep 15;172:73-79. doi: 10.1016/j.theriogenology.2021.06.008. Epub 2021 Jun 8.
During cryopreservation sperm encounter oxidative stress due to higher production of ROS molecules and insufficient natural antioxidant defence system. Therefore, present study was designed to identify the effects of various glutathione (GSH) concentrations on Indian red jungle fowl (Gallus gallus murghi) sperm quality and fertility pre-freezing and post-thaw incubation hours. Semen was collected from eight cocks and qualified semen ejaculates having motility >65% were pooled after initial evaluation. Semen was divided in four aliquots, diluted with red fowl extender (1:5) at 37 °C having GSH 0 mM (control), 0.1 mM, 0.5 mM and 1.0 mM, cryopreserved and stored at (-196 °C) in liquid nitrogen. Semen quality was assessed at post dilution, cooling, equilibration, and freeze-thawing at 0, 2 and 4 h of incubation at 37 °C. Sperm motility, plasma membrane integrity, viability, acrosome integrity and mitochondrial function were recorded highest (P < 0.05) with 0.5 mM GSH in extender at post-dilution, cooling, equilibration, freeze-thawing and 0, 2 and 4 h of incubation. Lipid peroxidation in sperm and seminal plasma were recorded lowest (P < 0.05) with 0.5 mM GSH during cryopreservation stages and post-thawing incubation. Moreover, antioxidant activities (total antioxidant potential and free radical scavenging capacity) were recorded highest (P < 0.05) in extender having 0.5 mM GSH. Fertility rates were recorded higher (P < 0.05) with 0.5 mM GSH compared to control. It is concluded that 0.5 mM GSH in extender improves sperm structural (sperm viability, plasma membrane integrity and acrosome integrity), functional integrity (motility, mitochondrial function) and fertility parameters of Indian red jungle fowl through enriching antioxidant potential and ameliorating the oxidative stress.
在冷冻保存过程中,精子由于 ROS 分子的产生增加和天然抗氧化防御系统不足而遭遇氧化应激。因此,本研究旨在确定不同谷胱甘肽 (GSH) 浓度对印度红原鸡(Gallus gallus murghi)精子质量和预冷冻和解冻后孵育时间的影响。从八只公鸡中采集精液,在初步评估后将活力>65%的合格精液射精物混合在一起。将精液分成四份,在 37°C 用红原鸡稀释剂(1:5)稀释,含有 0mM(对照)、0.1mM、0.5mM 和 1.0mM 的 GSH,然后冷冻保存并储存在 (-196°C) 液氮中。在稀释后、冷却、平衡和冷冻-解冻时,在 37°C 孵育 0、2 和 4 小时后评估精液质量。在稀释后、冷却、平衡、冷冻-解冻以及 0、2 和 4 小时孵育时,添加 0.5mM GSH 的稀释剂中记录到最高的精子活力、质膜完整性、活力、顶体完整性和线粒体功能(P<0.05)。在冷冻保存阶段和解冻后孵育期间,用 0.5mM GSH 处理的精子和精浆中的脂质过氧化反应最低(P<0.05)。此外,添加 0.5mM GSH 的稀释剂中的抗氧化活性(总抗氧化能力和自由基清除能力)最高(P<0.05)。用 0.5mM GSH 处理的受精率也高于对照组(P<0.05)。综上所述,在稀释剂中添加 0.5mM GSH 通过增加抗氧化能力和改善氧化应激,提高了印度红原鸡的精子结构(精子活力、质膜完整性和顶体完整性)、功能完整性(活力、线粒体功能)和生育参数。