Lee A-Sung, Lee Sang-Hee, Lee Seunghyung, Yang Boo-Keun
College of Animal Life Sciences, Kangwon National University, Chuncheon, 24341, Republic of Korea.
Institute of Animal Resources, Kangwon National University, Chuncheon, 24341, Republic of Korea.
Trop Anim Health Prod. 2020 Jan;52(1):437-444. doi: 10.1007/s11250-019-01983-2. Epub 2019 Jul 12.
This study investigated the effects of streptozotocin (STZ) and S-allyl-L-cysteine (SAC) on motility, plasma membrane integrity, and mitochondrial activity of the boar sperm. STZ (0, 10, 50, and 100 μM) and SAC (0, 1, 5, 25, and 100 μM) were treated alone and co-treated in the fresh boar semen. The motility, plasma membrane integrity, and mitochondrial activity of sperm were analyzed at 3, 6, and 9 h after incubation. Boar semen was collected using the gloved-hand method from ten crossbred male pigs, and age of experimental ten male pigs is 24~27 months. The sperm plasma membrane integrity was analyzed using Live/Dead sperm kit. Mitochondrial activity was analyzed using rhodamine 123 and PI double-staining method. Additionally, sperm motility was evaluated according to standard method. Sperm motility, plasma membrane integrity, and mitochondrial activity were decreased in an STZ concentration-dependent manner (P < 0.05) and also were decreased by 10 μM STZ in all incubation times (P < 0.05). The motility, plasma membrane integrity, and mitochondrial activity of the sperm were increased at 5 μM SAC treatment, whereas it was decreased at 100 μM treatment. In addition, sperm motility, plasma membrane integrity, and mitochondrial activity were increased when co-treated with 50 μM STZ and 5 μM SAC group at 9 h after incubation (P < 0.05). Based on our results, STZ has a deleterious effect on sperm characteristics, and SAC can protect sperm motility, viability, and function of the sperm exposed to STZ.
本研究调查了链脲佐菌素(STZ)和S-烯丙基-L-半胱氨酸(SAC)对公猪精子活力、质膜完整性和线粒体活性的影响。将STZ(0、10、50和100 μM)和SAC(0、1、5、25和100 μM)单独处理并在新鲜公猪精液中联合处理。在孵育3、6和9小时后分析精子的活力、质膜完整性和线粒体活性。采用戴手套采精法从10头杂交公猪采集精液,10头实验公猪的年龄为24至27个月。使用活/死精子试剂盒分析精子质膜完整性。采用罗丹明123和碘化丙啶双染法分析线粒体活性。此外,根据标准方法评估精子活力。精子活力、质膜完整性和线粒体活性以STZ浓度依赖性方式降低(P<0.05),并且在所有孵育时间,10 μM STZ也会使其降低(P<0.05)。在5 μM SAC处理时,精子的活力、质膜完整性和线粒体活性增加,而在100 μM处理时则降低。此外,在孵育9小时后,50 μM STZ和5 μM SAC联合处理组的精子活力、质膜完整性和线粒体活性增加(P<0.05)。根据我们的结果,STZ对精子特性有有害影响,而SAC可以保护暴露于STZ的精子的活力、生存能力和功能。