Suppr超能文献

添加神经生长因子对冷却后羊驼精子特性的影响。

Effects of NGF Addition on Llama () Sperm Traits After Cooling.

作者信息

Sari Luciana M, Zampini Renato, Gonzalez Del Pino Francisco, Argañaraz Martin E, Ratto Marcelo H, Apichela Silvana A

机构信息

Facultad de Bioquímica, Química y Farmacia, Instituto Superior de Investigaciones Biológicas (INSIBIO), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto de Biología "Dr. Francisco D. Barbieri" Universidad Nacional de Tucumán (UNT), San Miguel de Tucumán, Argentina.

Cátedra de Biología Celular y Molecular, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán, San Miguel de Tucumán, Argentina.

出版信息

Front Vet Sci. 2021 Jan 5;7:610597. doi: 10.3389/fvets.2020.610597. eCollection 2020.

Abstract

To provide new insights into the mechanisms through which seminal plasma proteins can protect sperm from damage caused during refrigeration, we evaluate the possibility that β-NGF can contribute to the improvement of sperm quality after cooling. First, β-NGF was detected in refrigerated sperm and compared with unrefrigerated sperm by western blotting of the proteins adsorbed by sperm, showing that native β-NGF is still present even 24 h after cooling only as an active form. Then, the effect of exogenous β-NGF on sperm quality after cooling was evaluated. A total of 12 ejaculates from male llamas (three ejaculates per male), were obtained by electro-ejaculation, diluted 4:1 with buffer Hepes-balanced salt solution and centrifuged at 800 × g for 8 min to remove the seminal plasma. Sperm were suspended in Tris-citrate-fructose-egg yolk diluent for a final concentration of 30 ×10/ml and cooled at 5°C for 24 h. After refrigeration, the extended sperm were equilibrated for 5 min at 37°C and divided into the following subgroups: sperm samples without treatment (control) and sperm samples supplemented with exogenous human β-NGF (10, 100, and 500 ng/ml). At 5, 30, and 60 min of incubation sperm were evaluated for sperm viability (using eosin/nigrosin stain), sperm motility and vigor (observed under light microscopy), and mitochondrial activity (using the JC-1 fluorescent marker). Vigor data were analyzed with the nonparametric Kruskal-Wallis test. The rest of the variables were analyzed with a mixed models approach. Mean comparisons were performed using Fisher's LSD test with a confidence level of 95%. A principal components analysis was performed to analyze the relationships between variables. Treatment of 24 h cooled sperm with 10 or 100 ng/ml of human β-NGF increased the percentage of total motility and vigor ( < 0.05). Besides, an incubation time of 60 min would be adequate to improve sperm quality, since all variables are positively related. The significant improvement observed in the motility and vigor of post-refrigerated sperm suggests that supplementation with exogenous β-NGF may be profitable for the improvement of cooled llama sperm.

摘要

为了深入了解精浆蛋白保护精子免受冷藏过程中损伤的机制,我们评估了β-神经生长因子(β-NGF)有助于改善精子冷却后质量的可能性。首先,通过对精子吸附的蛋白质进行蛋白质免疫印迹,在冷藏精子中检测β-NGF,并与未冷藏精子进行比较,结果表明,即使在冷却24小时后,天然β-NGF仍以活性形式存在。然后,评估外源性β-NGF对精子冷却后质量的影响。通过电刺激射精从雄性美洲驼中获取总共12份精液(每只雄性3份精液),用缓冲的Hepes平衡盐溶液按4:1稀释,并以800×g离心8分钟以去除精浆。将精子悬浮在柠檬酸-果糖-蛋黄稀释液中,最终浓度为30×10⁶/ml,并在5°C下冷却24小时。冷藏后,将稀释后的精子在37°C下平衡5分钟,并分为以下亚组:未处理的精子样本(对照)和补充外源性人β-NGF(10、100和500 ng/ml)的精子样本。在孵育5、30和60分钟时,评估精子活力(使用伊红/黑色素染色)、精子运动能力和活力(在光学显微镜下观察)以及线粒体活性(使用JC-1荧光标记)。活力数据采用非参数Kruskal-Wallis检验进行分析。其余变量采用混合模型方法进行分析。使用Fisher最小显著差异检验进行均值比较,置信水平为95%。进行主成分分析以分析变量之间的关系。用10或100 ng/ml的人β-NGF处理冷却24小时的精子可提高总运动能力和活力的百分比(P<0.05)。此外,60分钟的孵育时间足以改善精子质量,因为所有变量均呈正相关。冷藏后精子运动能力和活力的显著改善表明,补充外源性β-NGF可能有利于改善冷却后的美洲驼精子质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90e5/7814774/3bf2d021b439/fvets-07-610597-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验