在精液扩展剂中添加金属纳米颗粒对埃及水牛(Bubalus bubalis)精子解冻后质量和受精能力的影响

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-10 DOI:10.1007/s12011-024-04348-5
Wael A. Khalil, Mohamed S. El-Rais, Mohamed M. Hegazy, Mahmoud A. E. Hassan, Ali A. El-Raghi, Mostafa M. El-Moghazy
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引用次数: 0

摘要

纳米材料在农场动物繁殖领域具有广阔的应用前景,如转基因、向精子细胞精确输送物质、抗菌、抗氧化特性以及在改进冷冻保存方法方面的强大作用。本研究旨在探索在精液扩展剂中添加 10 µg/mL 纳米金(Au-NPs10)、10 µg/mL 纳米银(Ag-NPs10)、1 µg/mL 纳米硒(Se-NPs1)和 100 µg/mL 纳米硒(Se-NPs2)的效果、和 100 µg/mL 纳米氧化锌(ZnO-NPs100)对冷冻解冻水牛精子的精子特征和运动学参数、顶体完整性、氧化生物标志物、形态和凋亡样变化的影响,以及最终对其受精能力的影响。结果表明,与对照组相比,上述所有纳米材料都能显著提高解冻后水牛精子的活力、渐进运动性、膜完整性、顶体完整性、运动学参数以及类凋亡变化(p <0.05)。在扩展剂中添加这些金属纳米颗粒后,精子超微结构形态测量没有观察到明显的影响。与对照组相比,Au-NPs10、Ag-NPs10、Se-NPs1 和 ZnO-NPs100 处理组的 caspase 3 值分别显著降低了 64.22%、45.99%、75.59% 和 49.39%。与对照组相比,在扩展剂中添加 100 µg ZnO-NPs 可显著降低细菌、真菌和酵母菌的总计数(p < 0.05)。AuNPs10 和 SeNPs1 处理组显示,解冻后的扩展精液中丙二醛、过氧化氢和一氧化氮的含量较低,总抗氧化能力的值较高(p < 0.05)。与对照组相比,用 ZnO-NPs100、Se-NPs1 和 Au-NPs10 处理过的精子进行人工授精的水牛的受孕率分别提高了 17.5%、20% 和 30%。本研究结果表明,添加金属纳米颗粒的冷冻扩展剂是提高水牛精子冷冻耐受性和受精潜力的有效策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Effect of Metallic Nanoparticles Supplementation in Semen Extender on Post-thaw Quality and Fertilizing Ability of Egyptian Buffalo (Bubalus bubalis) Spermatozoa

Nanomaterials offer several promising prospects in the field of farm animal reproduction, encompassing a broad range of applications such as transgenesis and the precise delivery of substances to sperm cells, antimicrobial, antioxidants properties as well as their potent role in improving cryopreservation methods. The aim of the present study is to explore the effect of supplementing the semen extender with 10 µg/mL nano gold (Au-NPs10), 10 µg/mL nano silver (Ag-NPs10), 1 µg/mL nano selenium (Se-NPs1), and 100 µg/mL nano zinc oxide (ZnO-NPs100) on sperm characteristics and kinematics parameters, acrosome integrity, oxidative biomarkers, morphological and apoptosis-like changes of frozen-thawed buffalo bull sperm, and, ultimately, their fertilizing capacity. The results revealed that all aforementioned nano materials significantly improved viability, progressive motility, membrane integrity, acrosome integrity, and kinematic parameters as well as apoptosis-like changes of post-thawed buffalo bull sperm compared to the control (p < 0.05). No discernible effects were observed on sperm ultrastructure morphology measures as a response to the addition of these metallic nanoparticles to the extender. The values of caspase 3 significantly decreased by 64.22, 45.99, 75.59, and 49.39% in Au-NPs10, Ag-NPs10, Se-NPs1, and ZnO-NPs100 treated groups, respectively, compared to the control. The addition of 100 µg ZnO-NPs to the extender significantly decreased the total count of bacteria, fungi, and yeast compared to the control (p < 0.05). The AuNPs10 and SeNPs1 treated groups showed lower content of malondialdehyde, hydrogen peroxide, and nitric oxide concentrations and higher values of total antioxidant capacity of post-thawed extended semen (p < 0.05). Pregnancy rates increased by 17.5, 20, and 30% in buffalo cows inseminated with sperm treated with ZnO-NPs100, Se-NPs1, and Au-NPs10, respectively, compared to the control group. The present results indicate that the freezing extender supplemented with metallic nanoparticles can be an effective strategy to enhance the cryotolerance and fertility potential of buffalo bull sperm.

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