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首页> 外文期刊>Reproductive BioMedicine Online >Elevated NaCl concentration improves cryotolerance and developmental competence of porcine oocytes
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Elevated NaCl concentration improves cryotolerance and developmental competence of porcine oocytes

机译:升高的NaCl浓度可改善猪卵母细胞的耐低温性和发育能力

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摘要

High hydrostatic pressure has been reported to improve the fertilizing or developmental ability of mammalian spermatozoa, oocytes and embryos. This study investigated the effect of another stress, temporarily increased NaCl concentration, on cryotolerance and developmental competence of porcine oocytes. In Experiment 1, survival rates were compared after 1 h exposure to seven elevated NaCl concentrations and 1 h recovery time. In Experiment 2, oocytes were exposed to 593 and 1306 mOsmol NaCl, subsequently recovered, vitrified, then subjected to parthenogenetic activation. Both cleavage and blastocyst rates increased after NaCl treatment compared with untreated controls. In Experiment 3, oocytes were treated with 593 mOsmol NaCl followed by 1 and 2 h recovery, respectively, then used as recipients for somatic cell nuclear transfer (SCNT). Cleavage rates were not different from those in untreated controls, but blastocyst rates increased in both NaCl-treated groups. In conclusion, treatment of porcine oocytes with elevated NaCl concentrations improved their developmental competence after vitrification and parthenogenetic activation or SCNT. Further experiments are required to investigate in-vivo consequences, and the effect on gametes and embryos of different mammalian species.
机译:据报道,高静水压力可改善哺乳动物精子,卵母细胞和胚胎的受精或发育能力。这项研究调查了暂时性增加NaCl浓度的另一种应激对猪卵母细胞低温耐受性和发育能力的影响。在实验1中,比较了暴露于7种升高的NaCl浓度1 h和恢复1 h后的存活率。在实验2中,将卵母细胞暴露于593和1306 mOsmol的NaCl中,随后进行回收,玻璃化,然后进行孤雌生殖活化。与未处理的对照组相比,NaCl处理后的卵裂率和囊胚率均增加。在实验3中,分别用593 mOsmol NaCl处理卵母细胞,然后分别恢复1和2 h,然后将其用作体细胞核移植(SCNT)的受体。卵裂率与未治疗的对照组无差异,但两个NaCl治疗组的囊胚率均增加。总之,用高浓度的NaCl处理猪卵母细胞可提高其玻璃化和孤雌激活或SCNT后的发育能力。需要进一步的实验来研究体内后果,以及对不同哺乳动物物种的配子和胚胎的影响。

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  • 来源
    《Reproductive BioMedicine Online》 |2009年第3期|360-366|共7页
  • 作者单位

    Population Genetics and Embryology, Institute of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark Institute of Human Genetics, University of Aarhus, DK-8000 Aarhus, Denmark Beijing Genomics Institute, Airport-Industrial zone B-6, Beijing 101300, China;

    Population Genetics and Embryology, Institute of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark Institute of Human Genetics, University of Aarhus, DK-8000 Aarhus, Denmark Beijing Genomics Institute, Airport-Industrial zone B-6, Beijing 101300, China;

    Population Genetics and Embryology, Institute of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark;

    Population Genetics and Embryology, Institute of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark Institute of Human Genetics, University of Aarhus, DK-8000 Aarhus, Denmark;

    Population Genetics and Embryology, Institute of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark;

    Nutrition and Production Physiology, Institute of Animal Health, Welfare and Nutrition, Faculty of Agricultural Sciences, University of Aarhus, DK-8830 Tjele, Denmark;

    Kato Ladies' Clinic, Nishishinjuku, Shinjuku, Tokyo 160-0023, Japan;

    Beijing Genomics Institute, Airport-Industrial zone B-6, Beijing 101300, China;

    Beijing Genomics Institute, Airport-Industrial zone B-6, Beijing 101300, China;

    Institute of Human Genetics, University of Aarhus, DK-8000 Aarhus, Denmark;

    PIVET Medical Centre, 166-168 Cambridge Street, Leederville, Perth, WA 6007, Australia;

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