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      Alpha‐lipoic acid improves the maturation and the developmental potential of goat oocytes in vitro

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      https://www.riss.kr/link?id=O111859591

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2021년

      • 작성언어

        -

      • Print ISSN

        0936-6768

      • Online ISSN

        1439-0531

      • 등재정보

        SCI;SCIE;SCOPUS

      • 자료형태

        학술저널

      • 수록면

        545-554   [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]

      • 구독기관
        • 전북대학교 중앙도서관  
        • 성균관대학교 중앙학술정보관  
        • 부산대학교 중앙도서관  
        • 전남대학교 중앙도서관  
        • 제주대학교 중앙도서관  
        • 중앙대학교 서울캠퍼스 중앙도서관  
        • 인천대학교 학산도서관  
        • 숙명여자대학교 중앙도서관  
        • 서강대학교 로욜라중앙도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      다국어 초록 (Multilingual Abstract)

      Oxidative stress inevitably occurs during oocyte maturation in vitro. α‐lipoic acid (α‐LA) has a strong antioxidant capacity, but the effect of α‐LA on parthenogenetic activation of oocytes was rarely reported. This study aims to investigate the effect of supplementing α‐LA to in vitro maturation medium on the subsequent developmental ability of goat parthenogenetic embryos during oocytes maturation. In the study, the goat cumulus‐oocyte complex was divided into the experimental (with 25 μmol/L α‐LA) and the control (without α‐LA) groups. Oxidase expression was measured using RT‐qPCR. After 18–22 hr of maturation, the oocytes were then parthenogenetic activated. The total antioxidant capacity of embryos was measured after 0, 24, 48, 72 and 96 hr of culture. Rates of oocyte maturation and the rates of development for parthenogenetic embryos in the α‐LA group were significantly improved by 7.88% (p < .05) and 5.41% (p < .05) compared with those in the control group, respectively. After 24 hr, the difference in total antioxidant capacity was extremely significant in both groups. An evident decrease in the control group and a minor decrease in the α‐LA group were observed (p < .01). The ratio of inner cell mass cells to the total cell number of blastocysts in the α‐LA group increased compared with that in the control group (p < .05) on day 8. α‐LA significantly promoted the expression of SOD and GPX4 of parthenogenetic blastocysts and maturated oocytes. α‐LA (25 μmol/L) improved the maturation rate and the developmental competence of the parthenogenetic activation of oocytes, which might be mediated by maintaining the total antioxidant ability of oocytes during the culture period.
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      Oxidative stress inevitably occurs during oocyte maturation in vitro. α‐lipoic acid (α‐LA) has a strong antioxidant capacity, but the effect of α‐LA on parthenogenetic activation of oocytes was rarely reported. This study aims to investigate ...

      Oxidative stress inevitably occurs during oocyte maturation in vitro. α‐lipoic acid (α‐LA) has a strong antioxidant capacity, but the effect of α‐LA on parthenogenetic activation of oocytes was rarely reported. This study aims to investigate the effect of supplementing α‐LA to in vitro maturation medium on the subsequent developmental ability of goat parthenogenetic embryos during oocytes maturation. In the study, the goat cumulus‐oocyte complex was divided into the experimental (with 25 μmol/L α‐LA) and the control (without α‐LA) groups. Oxidase expression was measured using RT‐qPCR. After 18–22 hr of maturation, the oocytes were then parthenogenetic activated. The total antioxidant capacity of embryos was measured after 0, 24, 48, 72 and 96 hr of culture. Rates of oocyte maturation and the rates of development for parthenogenetic embryos in the α‐LA group were significantly improved by 7.88% (p < .05) and 5.41% (p < .05) compared with those in the control group, respectively. After 24 hr, the difference in total antioxidant capacity was extremely significant in both groups. An evident decrease in the control group and a minor decrease in the α‐LA group were observed (p < .01). The ratio of inner cell mass cells to the total cell number of blastocysts in the α‐LA group increased compared with that in the control group (p < .05) on day 8. α‐LA significantly promoted the expression of SOD and GPX4 of parthenogenetic blastocysts and maturated oocytes. α‐LA (25 μmol/L) improved the maturation rate and the developmental competence of the parthenogenetic activation of oocytes, which might be mediated by maintaining the total antioxidant ability of oocytes during the culture period.

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