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利用凝集素花生凝集素(PNA)-磁性纳米颗粒对顶体受损的驴精子进行纳米耗竭。

Nano-depletion of acrosome-damaged donkey sperm by using lectin peanut agglutinin (PNA)-magnetic nanoparticles.

机构信息

Veterinary Reproduction Group, Department of Animal Medicine and Surgery, University of Cordoba, Cordoba, 14071, Spain; Department of Theriogenology, Faculty of Veterinary Medicine, Assiut University, Assiut, Egypt.

Departamento de Química Analítica, Instituto Universitario de Investigación en Química Fina y Nanoquímica IUNAN, Universidad de Córdoba, Campus de Rabanales, Edificio Marie Curie, E-14071, Córdoba, Spain.

出版信息

Theriogenology. 2020 Jul 15;151:103-111. doi: 10.1016/j.theriogenology.2020.04.011. Epub 2020 Apr 14.

Abstract

Lectin is considered as a suitable biomarker for nano-depletion of acrosome-damaged sperm. The aim of this study was to synthetize magnetic nanoparticles (MNPs) coated by peanut (Arachis hypogaea) agglutinin lectin (PNA) and investigate its beneficial effect in improving of sperm characteristics. MNPs were obtained by co-precipitation method, functionalized with chitosan and coated by PNA at a concentration of 0.04 mg/mL. Semen was frozen either with glycerol-based or sucrose-based extenders. Frozen-thawed straws from five donkeys (three ejaculates per donkey) were incubated with lectin-MNPs (2 mg/mL), and then exposed to an external magnet enabling the non-bound sperm to be collected as nanopurified sperm. Sperm were evaluated post-thawing (control) and after nanopurification for motility, plasma membrane integrity, acrosome integrity, morphology, DNA fragmentation and concentration. The statistical analyses were extended to investigate the correlation between the initial quality of the frozen-thawed semen samples and the effect of nanopurification after thawing. The obtained MNPs were biocompatible to the sperm and significantly improved the progressive motility (P < 0.05) for the glycerol nanopurified group (43.08 ± 3.52%) in comparison to control (33.70 ± 2.64%). Acrosome-damaged sperm were reduced (P < 0.05) in both nanopurified groups (19.92 ± 2.69 for G and 21.57 ± 2.77 for S) in comparison to control (36.07 ± 3.82 for G and 35.35 ± 3.88 for S). There were no significant changes in sperm morphology and membrane integrity after nanopurification. The average sperm recovery after nanopurification was 80.1%. Sperm quality index was significantly higher (P < 0.001) in nanopurified groups regardless of the initial quality of the frozen thawed semen samples. However, in the high sperm quality group, nanopurification significantly improved the progressive motility and membrane integrity besides the increasing of acrosome-intact sperm. Sperm nanopurification using lectin-magnetic nanoparticles can be considered as a suitable method to reduce the proportion of acrosome-damaged sperm and to increase the quality of frozen thawed donkey semen.

摘要

凝集素被认为是一种合适的生物标志物,可用于检测顶体受损的精子的纳米耗竭。本研究的目的是合成被花生凝集素(PNA)包被的磁性纳米颗粒(MNPs),并研究其改善精子特性的有益效果。MNPs 通过共沉淀法获得,用壳聚糖功能化,并在 0.04mg/mL 的浓度下用 PNA 包被。精液用甘油基或蔗糖基稀释液冷冻。从五头驴(每头驴 3 个射精)中冷冻的 straw 用凝集素-MNPs(2mg/mL)孵育,然后暴露于外部磁场,以使未结合的精子被收集为纳米纯化的精子。解冻后(对照)和纳米纯化后评估精子的活力、质膜完整性、顶体完整性、形态、DNA 碎片化和浓度。统计分析扩展到研究冷冻解冻精液样本的初始质量与解冻后纳米纯化效果之间的相关性。获得的 MNPs 对精子具有生物相容性,并显著提高了甘油基纳米纯化组的前向运动能力(P<0.05)(43.08±3.52%)与对照组(33.70±2.64%)相比。在两个纳米纯化组中(G 组为 19.92±2.69,S 组为 21.57±2.77),顶体受损的精子减少(P<0.05)与对照组(G 组为 36.07±3.82,S 组为 35.35±3.88)相比。纳米纯化后精子形态和质膜完整性没有显著变化。纳米纯化后的平均精子回收率为 80.1%。无论冷冻解冻精液样本的初始质量如何,精子质量指数在纳米纯化组中均显著升高(P<0.001)。然而,在高精子质量组中,纳米纯化除了增加完整顶体的精子外,还显著改善了前向运动和质膜完整性。使用凝集素-磁性纳米颗粒对精子进行纳米纯化可以被认为是一种减少顶体受损精子比例和提高冷冻解冻驴精液质量的合适方法。

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