Nohalez A, Martinez C A, Parrilla I, Roca J, Gil M A, Rodriguez-Martinez H, Martinez E A, Cuello C
Faculty of Veterinary Medicine, International Excellence Campus for Higher Education and Research "Campus Mare Nostrum", University of Murcia, Murcia, Spain; Institute for Biomedical Research of Murcia (IMIB-Arrixaca), Murcia, Spain.
Department of Clinical & Experimental Medicine (IKE), Linköping University, Linköping, Sweden.
Theriogenology. 2018 Jun;113:113-119. doi: 10.1016/j.theriogenology.2018.02.014. Epub 2018 Feb 16.
In this study, the effects of addition of the antioxidant ascorbic acid (AsA) were evaluated during porcine in vitro embryo production (IVP) and vitrification. In experiment 1, the effects of AsA supplementation during IVM, IVF and IVC were evaluated, using a total of 2744 oocytes in six replicates. The IVM, IVF and embryo IVC media were supplemented or not (control) with 50 μg/mL AsA in all possible combinations. No significant effects of AsA were detected in any of the maturation, fertilization or embryo development parameters assessed. In experiment 2, we evaluated the effects of adding AsA to vitrification-warming media on the post-warming survival and quality of blastocysts. Day-6 in vitro-produced blastocysts (N = 588) from six replicates were randomly divided in two groups, with vitrification and warming media either supplemented with 50 μg/mL AsA (VW + group) or un-supplemented (VW- control). Addition of AsA increased (P < 0.05) blastocyst survival rate after vitrification compared with that of VW- control embryos. Vitrification and warming increased (P < 0.05) the production of oxygen species (ROS) and reduced (P < 0.05) the glutathione levels in blastocysts. Although VW + blastocysts displayed higher (P < 0.05) ROS levels than those of fresh control blastocysts, the levels were lower (P < 0.05) than those found in VW- control blastocysts. In conclusion, under the experimental conditions, supplementation of IVM/IVF/IVC media with AsA did not improve the embryo production in vitro. By contrast, the addition of AsA to chemically defined vitrification and warming media increased the survival of in vitro-produced porcine blastocysts by decreasing ROS production.
在本研究中,评估了在猪体外胚胎生产(IVP)和玻璃化过程中添加抗氧化剂抗坏血酸(AsA)的效果。在实验1中,评估了在体外成熟(IVM)、体外受精(IVF)和体外培养(IVC)过程中添加AsA的效果,共使用2744个卵母细胞,分为六个重复组。IVM、IVF和胚胎IVC培养基以所有可能的组合添加或不添加(对照)50μg/mL的AsA。在所评估的任何成熟、受精或胚胎发育参数中均未检测到AsA的显著影响。在实验2中,我们评估了在玻璃化-复温培养基中添加AsA对复温后囊胚存活率和质量的影响。来自六个重复组的第6天体外产生的囊胚(N = 588)被随机分为两组,玻璃化和复温培养基分别添加50μg/mL的AsA(VW +组)或不添加(VW -对照组)。与VW -对照胚胎相比,添加AsA提高了(P < 0.05)玻璃化后囊胚的存活率。玻璃化和复温增加了(P < 0.05)囊胚中活性氧(ROS)的产生,并降低了(P < 0.05)谷胱甘肽水平。尽管VW +囊胚的ROS水平高于新鲜对照囊胚(P < 0.05),但低于VW -对照囊胚中的水平(P < 0.05)。总之,在实验条件下,在IVM/IVF/IVC培养基中添加AsA并不能提高体外胚胎生产效率。相比之下,在化学定义的玻璃化和复温培养基中添加AsA可通过减少ROS产生提高体外产生的猪囊胚的存活率。