Lee Han-Bi, Lee Seung-Eun, Park Min-Jee, Han Dong-Hun, Lim Eun-Seo, Ryu Bokyeong, Kim Eun-Young, Park Se-Pill
Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, 102 Jejudaehak-ro, Jeju, Jeju Special Self-Governing Province, 63243, South Korea; Stem Cell Research Center, Jeju National University, 102 Jejudaehak-ro, Jeju, Jeju Special Self-Governing Province, 63243, South Korea.
Department of Bio Medical Informatic, College of Applied Life Sciences, Jeju National University, 102 Jejudaehak-ro, Jeju, Jeju Special Self-Governing Province, 63243, South Korea; Cronex Co., 110 Hwangtalli-gil, Gangnae-myeon, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do, 28174, South Korea.
Theriogenology. 2024 Feb;215:214-223. doi: 10.1016/j.theriogenology.2023.12.001. Epub 2023 Dec 12.
Ellagic acid (EA) is a natural polyphenol and a free radical scavenger with antioxidant properties. This study investigated the protective effects of EA during in vitro maturation (IVM) of porcine oocytes. To determine the optimal concentration, IVM medium was supplemented with various concentrations of EA. Treatment with 10 μM EA (10 EA) resulted in the highest cleavage rate, blastocyst formation rate, and total cell number per blastocyst and the lowest percentage of apoptotic cell in parthenogenetic blastocysts. In the 10 EA group, abnormal spindle and chromosome misalignment were rescued and the ratio of phosphorylated p44/42 to total p44/42 was increased. Furthermore, the reactive oxygen species and glutathione levels were significantly decreased and increased, respectively, and antioxidant genes (Nrf2, HO-1, CAT, and SOD1) were significantly upregulated in the 10 EA group. mRNA expression of developmental-related (CDX2, POU5F1, and SOX2) and anti-apoptotic (BCL2L1) genes was significantly upregulated in the 10 EA group, while mRNA expression of pro-apoptotic genes (BAK, FAS, and CASP3) was significantly downregulated. Ultimately, following somatic cell nuclear transfer, the blastocyst formation rate was significantly increased and the percentage of apoptotic cell in blastocysts was significantly decreased in the 10 EA group. In conclusion, addition of 10 EA to IVM medium improved oocyte maturation and the subsequent embryo development capacity through antioxidant mechanisms. These findings suggest that EA can enhance the efficiencies of assisted reproductive technologies.
鞣花酸(EA)是一种天然多酚,具有抗氧化特性,是一种自由基清除剂。本研究调查了EA在猪卵母细胞体外成熟(IVM)过程中的保护作用。为确定最佳浓度,在IVM培养基中添加了不同浓度的EA。用10μM EA(10EA)处理导致最高的卵裂率、囊胚形成率和每个囊胚的总细胞数,以及孤雌生殖囊胚中凋亡细胞的最低百分比。在10EA组中,异常纺锤体和染色体排列紊乱得到挽救,磷酸化p44/42与总p44/42的比率增加。此外,10EA组中的活性氧水平显著降低,而谷胱甘肽水平显著升高,抗氧化基因(Nrf2、HO-1、CAT和SOD1)显著上调。发育相关基因(CDX2、POU5F1和SOX2)和抗凋亡基因(BCL2L1)的mRNA表达在10EA组中显著上调,而促凋亡基因(BAK、FAS和CASP3)的mRNA表达显著下调。最终,在体细胞核移植后,10EA组的囊胚形成率显著增加,囊胚中凋亡细胞的百分比显著降低。总之,在IVM培养基中添加10EA可通过抗氧化机制改善卵母细胞成熟和随后的胚胎发育能力。这些发现表明EA可以提高辅助生殖技术的效率。