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dc.contributor.advisorBùi, Hồng Thủy
dc.contributor.advisorLê, Thu Hoài
dc.contributor.authorNguyễn, Ngọc Thảo Vy
dc.date.accessioned2025-02-21T07:18:21Z
dc.date.available2025-02-21T07:18:21Z
dc.date.issued2024-04
dc.identifier.urihttp://keep.hcmiu.edu.vn:8080/handle/123456789/6745
dc.description.abstractThe in vitro culturing process of porcine oocytes has increasingly drawn the attention of embryologists worldwide thanks to the species’ great similarity with humans as well as other cattle’s genomes, and thus, its potential contribution to a wide range of scientific expertise. The approach includes providing immature oocytes with an environment that mimics as perfectly as possible the in vivo niches, thus improving the quality and viability of the cultured reproductive cells. However, the culturing practices have reportedly been hampered by Reactive Oxygen Species (ROS) which are proven to be fatal for interfering with the cellular structures and processes, eventually decreasing the lateral competence of oocytes. Therefore, antioxidants are added as supplements to cope with the problem. Non-enzymatic antioxidants such as Melatonin and Astaxanthin have already been proven for their effectiveness on the in vitro maturation assay of oocytes. Nevertheless, their effects on the in vitro growth of early antral ones remain unanswered. My experiment focuses on exploring the effect of Astaxanthin and Melatonin on the in vitro growth of porcine early antral follicles’ (EAFs) oocytes via examining key genes’ expression. The application of low gelling agarose coating to better support the culture procedure exhibited remarkable effects. The result shows that antioxidant supplementation possibly improved the survival rates of IVG oocytes, proven by increased expression of anti-apoptosis BCl2 gene (though not significantly). As for in vitro maturation, although Astaxanthin did not affect the maturation rate, Melatonin seemed potential in improving the parameter, proven by adequate cumulus expansion and expression of related genes such as BMP15, BCl2, SOD-1, and CAT; nevertheless, more replicates need to be carried out to find out the most optimal concentration. In general, supplemented antioxidants had effects on the inner-cellular antioxidation system and improved oocyte quality via increased expression of gene related to growth, anti-apoptosis, and antioxidation enzyme. Astaxanthin is a potentially effective antioxidant alternative which can be applied for oocyte culturing practicesen_US
dc.subjectantioxidantsen_US
dc.subjectAstaxanthinen_US
dc.subjectMelatoninen_US
dc.subjectin vitro growth of oocytesen_US
dc.subjectgene expressionen_US
dc.subjectRT-qPCRen_US
dc.subjectmagnetic beads mRNA extractionen_US
dc.titleEffect Of Astaxanthin On Gene Expression Of Porcine Oocyte Derived From Early Antral Follicle After In Vitro Growthen_US
dc.typeThesisen_US


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