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Boar sperm changes after sorting and encapsulation in barium alginate membranes

机译:将公猪精子在藻酸钡膜中分选和包封后发生变化

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A routine use of boar-sexed semen is limited by the long sorting time necessary to obtain an adequate number of sexed spermatozoa for artificial insemination and by the high susceptibility of spermatozoa of this species to damages induced by sorting procedure and subsequent cryopreservation. The aim of this work was to study the impact of encapsulation in barium alginate membrane on sorted boar spermatozoa by evaluating membrane integrity, chlortetracycline staining patterns, protein tyrosine phosphorylation, and Hsp70 immunolocalization during storage over 72 hours in liquid or encapsulated form. The encapsulation procedure significantly (P < 0.05) decreased the overall membrane integrity of control unsorted semen (81.8 vs. 57.4, CTR vs. CPS), but did not negatively affect the overall viability and the chlortetracycline staining patterns of sorted encapsulated cells. Moreover, encapsulation significantly decreased (P < 0.05) the overall phosphotyrosin A pattern cell percentage in unsorted (98.4 vs. 92.6, CTR vs. CPS) but not in sorted semen (64.0 vs. 74.2; SORT CTR vs. SORT CPS). As for Hsp70, the overall percentage of cells displaying the different patterns was significantly influenced (P < 0.05) by treatment but not by storage time. The sorting procedure seems to induce the major changes, whereas encapsulation tends to exert a protective effect on sorted semen by increasing the percentage of spermatozoa displaying the T pattern (2.8 vs. 24.3; SORT CTR vs. SORT CPS). In conclusion, our data confirm that the damaging impact of the encapsulation in barium alginate capsules seems to be limited when compared with that of the sorting procedure and, moreover, the association of the two procedures does not result in an algebraic sum of the negative effects. These results suggest the possibility of a future utilization of the encapsulation technology in order to store sorted spermatozoa and permit their controlled release in the female genital tract
机译:公猪性精液的常规使用受到限制,因为要获得足够数量的有性别的精子进行人工授精所需要的漫长的分拣时间,以及该种精子对分选程序和随后的低温保存引起的损害的敏感性高。这项工作的目的是通过评估膜的完整性,金霉素的染色模式,蛋白酪氨酸磷酸化和以液体或胶囊形式储存72小时以上的Hsp70免疫定位,研究海藻酸钡薄膜中的胶囊封装对公猪精子的影响。封装过程显着(P <0.05)降低了对照未分选精液的整体膜完整性(81.8 vs. 57.4,CTR vs. CPS),但并未对分选的封装细胞的整体生存力和金霉素染色模式产生负面影响。此外,在未分选(98.4 vs. 92.6,CTR vs. CPS)中,封装显着降低(P <0.05)总体磷酸酪氨酸A型细胞百分比,而在分选精液中则没有(64.0 vs. 74.2; SORT CTR vs. SORT CPS)。对于Hsp70,显示不同模式的细胞的总体百分比受处理的影响显着(P <0.05),但不受储存时间的影响。分选过程似乎引起了主要变化,而包囊则倾向于通过增加表现出T型分布的精子百分比来对分选的精液发挥保护作用(2.8 vs. 24.3; SORT CTR vs. SORT CPS)。总之,我们的数据证实,与分选程序相比,藻酸钡胶囊中封装的破坏性影响似乎是有限的,而且,这两种程序的结合不会导致负面影响的代数加总。 。这些结果表明将来有可能利用包囊技术来存储分选的精子并允许其在女性生殖道中受控释放。

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