Hallberg Ida, Morrell Jane M, Malaluang Pack, Johannisson Anders, Sjunnesson Ylva, Laskowski Denise
Department of Clinical Sciences, Centre for Reproductive Biology in Uppsala (CRU), Swedish University of Agricultural Sciences, Uppsala, Sweden.
Department of Animal Biosciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Front Vet Sci. 2024 Sep 13;11:1444550. doi: 10.3389/fvets.2024.1444550. eCollection 2024.
Since boar spermatozoa show a marked deterioration in sperm quality when cooled, insemination doses are usually stored at 16-18 °C. However, maintaining this temperature during transport of semen doses is challenging, particularly during the summer months. An alternative could be to store the doses at 4 °C if cold-shock to the sperm could be prevented. The objective of this study was to evaluate boar sperm quality and fertility in fertilization after storage in AndroStar Premium at 4 °C for 1 week.
Insemination doses ( = 9) in AndroStar Premium from a commercial boar semen collection station were transported to the laboratory at approximately 20 °C. At the laboratory, sperm quality evaluation and was preformed and each dose was split; half of each ejaculate was stored in a climate-controlled box at 16-18 °C, the other was slowly cooled to 4 °C. Both samples were stored for 1 week before further sperm quality evaluation and fertilization (IVF) were performed. Mean values were tested using generalized linear regression, with treatment and boar as fixed factors; ≤ 0.05 was considered significant.
Sperm membrane integrity (mean ± sem: 91 ± 0.05 and 83 ± 0.09% for 16 and 4 °C, respectively) and superoxide production (6.79 ± 2.37 and 13.54 ± 6.23% for 16 and 4 °C, respectively), were different between treatments. The DNA fragmentation index was lower in cold-stored samples than in conventionally stored samples (3.74 ± 2.25 and 7.40 ± 3.36% for 4 and 16 °C, respectively). The numbers of oocytes developing to blastocyst on Day 6 (mean ± sd: 9.0 ± 8.0 and 6.0 ± 5.0%, for storage at 16 and 4 °C, respectively) were not different between treatments.
Therefore, storage of boar semen doses in AndroStar Premium at 4 °C for up to 7 days would be a viable alternative to current praxis.
由于公猪精子在冷却时精子质量会显著下降,输精剂量通常在16 - 18°C下储存。然而,在精液剂量运输过程中维持这个温度具有挑战性,尤其是在夏季。如果能防止精子受到冷休克,另一种选择可能是将剂量储存在4°C。本研究的目的是评估公猪精液在AndroStar Premium中于4°C储存1周后的精子质量和受精后的生育能力。
来自商业公猪精液采集站的AndroStar Premium中的输精剂量(n = 9)在约20°C下运至实验室。在实验室进行精子质量评估并将每个剂量分开;每个射精量的一半储存在温度控制箱中于16 - 18°C,另一半缓慢冷却至4°C。两个样本在进一步进行精子质量评估和体外受精(IVF)之前均储存1周。使用广义线性回归测试平均值,将处理和公猪作为固定因素;P≤0.05被认为具有显著性。
处理之间精子膜完整性(平均值±标准误:16°C和4°C时分别为91±0.05%和83±0.09%)和超氧化物产生(16°C和4°C时分别为6.79±2.37%和13.54±6.23%)不同。冷储存样本中的DNA碎片化指数低于传统储存样本(4°C和16°C时分别为3.74±2.25%和7.40±3.36%)。在第6天发育成囊胚的卵母细胞数量(平均值±标准差:16°C和4°C储存时分别为9.0±8.0%和6.0±5.0%)在处理之间没有差异。
因此,将公猪精液剂量在AndroStar Premium中于4°C储存长达7天是当前做法的一个可行替代方案。