Zhu Zhendong, Li Wenjia, Zhao Haolong, Adetunji Adedeji Olufemi, Kamel Ahmed Mohamed, Min Lingjiang
College of Animal Science and Technology, Qingdao Agricultural University, Qingdao 266109, China.
Department of Agriculture, University of Arkansas at Pine Bluff, Pine Bluff, AR 71601, USA.
Animals (Basel). 2024 Dec 12;14(24):3592. doi: 10.3390/ani14243592.
This investigation aimed to study the effects of varying light exposure durations on ram sperm. A total of 25 rams were randomly divided into five groups. The control group was exposed to light durations of 12 h, while the experimental groups were exposed to light durations of 14, 16, 18, and 20 h. After three months of rearing, semen was collected from each ram four times using the artificial vagina method. The sperm motility parameters, sperm abnormality, sperm concentration, acrosome integrity, membrane integrity, semen volume, and total sperm number were measured. Thereafter, the metabolome, amino acid level, testosterone content, plasma follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels, and sperm antioxidant capacity were measured. The results showed that the sperm motility, sperm concentration, ejaculation volume, total sperm number, acrosome integrity, and membrane integrity in the 16 h light group were significantly improved compared to the control ( < 0.05), meanwhile the sperm abnormality was decreased. Moreover, we found 345 different metabolites between the control and 16 h light group. Among these, 273 were upregulated and 72 were downregulated. Furthermore, the amino acid content of the seminal plasma in the 16 h light group was significantly increased ( < 0.05) compared to the control. Interestingly, the seminal plasma testosterone content and the levels of FSH and LH in the serum in the 16 h light group were significantly increased ( < 0.05) compared to the control. In terms of the sperm antioxidant capacity, it was observed that the CAT activity was the highest in the group exposed to 16 h of light and decreased at 18 h of light exposure when compared to the control group; however, the CAT activity at 20 h was not different from the control. Additionally, within the 14 to 18 h light exposure range, prolonged light exposure increased the GSH content ( < 0.05), whereas 20 h of light exposure reduced the GSH content. The MDA levels decreased with prolonged light exposure, reaching the lowest point at 16 h ( < 0.05), but increased again at 20 h of light exposure. KEGG analysis indicated that the differential metabolites were mainly involved in metabolic and synthetic activities. Based on the results of this study, we can conclude that the artificial extension of the light duration for 16 h has a positive effect on ram sperm quality.
本研究旨在探讨不同光照时长对公羊精子的影响。将25只公羊随机分为五组。对照组光照时长为12小时,实验组光照时长分别为14、16、18和20小时。饲养三个月后,采用人工阴道法从每只公羊采集四次精液。测定精子活力参数、精子畸形率、精子浓度、顶体完整性、膜完整性、精液体积和总精子数。此后,测定代谢组、氨基酸水平、睾酮含量、血浆促卵泡激素(FSH)和促黄体生成素(LH)水平以及精子抗氧化能力。结果表明,与对照组相比,16小时光照组的精子活力、精子浓度、射精量、总精子数、顶体完整性和膜完整性均显著提高(P<0.05),同时精子畸形率降低。此外,我们发现对照组和16小时光照组之间有345种不同的代谢物。其中,273种上调,72种下调。此外,与对照组相比,16小时光照组精浆中的氨基酸含量显著增加(P<0.05)。有趣的是,与对照组相比, 16小时光照组的精浆睾酮含量以及血清中FSH和LH水平均显著增加(P<0.05)。在精子抗氧化能力方面,观察到与对照组相比,16小时光照组的CAT活性最高,18小时光照时降低;然而,20小时光照时的CAT活性与对照组无差异。此外,在14至18小时光照范围内,延长光照时间会增加GSH含量(P<0.05),而20小时光照会降低GSH含量。MDA水平随着光照时间延长而降低,在16小时时达到最低点(P<0.05),但在20小时光照时又再次升高。KEGG分析表明,差异代谢物主要参与代谢和合成活动。基于本研究结果,我们可以得出结论,人工延长光照时长至16小时对公羊精子质量有积极影响。