Akarsu Serkan Ali, Güngör İbrahim Halil, Cihangiroğlu Aslıhan Çakır, Acısu Tutku Can, Koca Recep Hakkı, Türk Gaffari, Sönmez Mustafa, Gür Seyfettin
Department of Reproduction and Artificial Insemination, Faculty of Veterinary Medicine, Ataturk University, Erzurum, Turkey.
Department of Reproduction and Artificial Insemination, Faculty of Veterinary Medicine, Fırat University, Elazığ, Turkey.
Anim Reprod. 2023 May 29;20(2):e20230001. doi: 10.1590/1984-3143-AR2023-0001. eCollection 2023.
In this study, it was aimed to determine the effect of sulforaphane (SFN) on rabbit semen cryopreservation. Semen collected from animals was divided into 5 equal volumes as Control, SFN 5 µM, SFN 10 µM, SFN 25 µM and SFN 50 µM groups. Afterwards, semen analyzes were performed. According to our results, there was no statistical difference between the groups at 4°C. However after freezing thawing, the highest total motility, progressive motility and rapid spermatozoa rate was seen in the 10 µM SFN group, while the lowest was observed in the 50 µM SFN group (P<0.05). Static sperm ratio was highest in the 50 µM group, while the lowest was observed in the 10 µM SFN group. When flow cytometry results examined the rate of acrosomal damaged and dead sperm was the lowest in the 10 µM SFN group, a statistical difference was observed between the control group (P<0.05). The highest rate of sperm with high mitochondrial membrane potential was seen in the 5 µM SFN and 10 µM SFN groups. Apoptosis and ROS rates were found to be lower in the experimental groups compared to the control groups (P<0.05). As a result, SFN supplementation at a dose of 10 µM increased the quality of sperm in the freezing and thawing processes of rabbit semen. In conclusion, 10 µM SFN improved the quality of cryopreservation of rabbit semen.
本研究旨在确定萝卜硫素(SFN)对兔精液冷冻保存的影响。从动物采集的精液被分成5等份,分别为对照组、5 μM SFN组、10 μM SFN组、25 μM SFN组和50 μM SFN组。之后,进行精液分析。根据我们的结果,4℃时各组之间无统计学差异。然而,冷冻解冻后,10 μM SFN组的总活力、前向运动率和快速精子率最高,而50 μM SFN组最低(P<0.05)。50 μM组的静态精子比例最高,而10 μM SFN组最低。流式细胞术结果显示,10 μM SFN组的顶体损伤和死精子率最低,与对照组之间存在统计学差异(P<0.05)。5 μM SFN组和10 μM SFN组的线粒体膜电位高的精子比例最高。与对照组相比,实验组的凋亡率和活性氧率较低(P<0.05)。结果表明,10 μM剂量的SFN补充剂可提高兔精液冷冻和解冻过程中的精子质量。总之,10 μM SFN改善了兔精液冷冻保存的质量。