Animal Reproduction Laboratory, Animal Sciences Institute, National Agricultural Research Center, Islamabad, Pakistan.
Cryo Letters. 2020 Jul-Aug;41(4):194-201.
Superoxide dismutase (SOD) as an antioxidant in semen extender may be used for the cryopreservation of buffalo spermatozoa and in vivo fertility.
This study was aimed to evaluate the effects of SOD (SOD1, 100 IU/mL; SOD2, 200 IU/mL; SOD3, 300 IU/mL) and control (0.0) in Tris citric acid extender on in vitro quality and in vivo fertility of cryopreserved water buffalo bull spermatozoa.
Semen collection was carried out on a weekly basis (four bulls, three replicates, and n = 24 ejaculates). The conventional freezing of semen loaded straws (0.5 mL) was undertaken by placing them horizontally on a steel rack inside a Styrofoam box for 10 min containing liquid nitrogen (LN2) vapours, and plunging into a liquid nitrogen tank (-196 °C) for storage, followed by thawing at 37 °C for 30 s and analysis by computer-assisted sperm analyzer (CASA) and other assays.
At post-dilution, the acrosome integrity (ACR-I, %) was significantly improved (P < 0.05) in extender supplemented with SOD3 as compared to other experimental groups. In addition, DNA integrity (DNA-I, %) was significantly higher (P < 0.05) in SOD1 and SOD3 compared to SOD2 and control. At post-thawing, the mean values of sperm progressive motility (PM, %), average path velocity (VAP, µm/s) and straight line velocity (VSL, µm/s) were significantly higher (P < 0.05) in extender supplemented with SOD3 compared to the control. At post-thawing, mean values of subjective motility (SM, %), plasma membrane integrity (PMI, %) and ACR-I were significantly higher (P < 0.05) in extender supplemented with SOD3 compared to the control. At post-thawing, sperm DNA-I was significantly higher (P < 0.05) in extender supplemented with all SOD doses compared to the control in a dose-dependent manner. The in vivo fertility rate (%) was significantly higher with SOD3 compared to the control (68.2 % vs. 49.5 %).
The supplementation of SOD3 (300 IU/mL) in Tris citric acid extender improves both in vitro quality and in vivo fertility of buffalo bull spermatozoa.
超氧化物歧化酶(SOD)作为精液稀释液中的抗氧化剂,可用于水牛精子的冷冻保存和体内受精。
本研究旨在评估 SOD(SOD1,100IU/mL;SOD2,200IU/mL;SOD3,300IU/mL)和对照(0.0)在Tris 柠檬酸稀释液对水牛公牛冷冻精子的体外质量和体内生育力的影响。
每周进行一次精液采集(4 头公牛,3 个重复,n=24 个射精)。将装载精液的细管(0.5mL)水平放置在泡沫盒内的钢架上 10 分钟,使细管内充满液氮(LN2)蒸气,然后将细管浸入液氮罐(-196°C)中储存,然后在 37°C 下解冻 30 秒,并通过计算机辅助精子分析仪(CASA)和其他检测进行分析。
在稀释后,与其他实验组相比,添加 SOD3 的稀释液中顶体完整率(ACR-I,%)显著提高(P<0.05)。此外,与 SOD2 和对照组相比,SOD1 和 SOD3 组的 DNA 完整率(DNA-I,%)显著升高(P<0.05)。在解冻后,添加 SOD3 的稀释液中精子的总运动速度(PM,%)、平均路径速度(VAP,µm/s)和直线速度(VSL,µm/s)的平均值显著升高(P<0.05)与对照组相比。在解冻后,添加 SOD3 的稀释液中主观运动(SM,%)、质膜完整性(PMI,%)和顶体完整率(ACR-I)的平均值显著高于对照组(P<0.05)。在解冻后,添加所有 SOD 剂量的稀释液中精子的 DNA-I 均显著高于对照组,呈剂量依赖性(P<0.05)。与对照组相比,SOD3 组的体内生育力(%)显著提高(68.2%比 49.5%)。
Tris 柠檬酸稀释液中添加 SOD3(300IU/mL)可提高水牛公牛精子的体外质量和体内生育力。