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Antioxidant supplementation overcomes the deleterious effects of maternal restraint stress-induced oxidative stress on mouse oocytes

机译:补充抗氧化剂克服了母体约束应激诱导的氧化应激对小鼠卵母细胞的有害影响

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In this study, using a mouse model, we tested the hypothesis that restraint stress would impair the developmental potential of oocytes by causing oxidative stress and that antioxidant supplementation could overcome the adverse effect of stress-induced oxidative stress. Female mice were subjected to restraint stress for 24?h starting 24?h after equine chorionic gonadotropin injection. At the end of stress exposure, mice were either killed to recover oocytes for in vitro maturation (IVM) or injected with human chorionic gonadotropin and caged with male mice to observe in vivo development. The effect of antioxidants was tested in vitro by adding them to IVM medium or in vivo by maternal injection immediately before restraint stress exposure. Assays carried out to determine total oxidant and antioxidant status, oxidative stress index, and reactive oxygen species (ROS) and glutathione levels indicated that restraint stress increased oxidative stress in mouse serum, ovaries, and oocytes. Whereas the percentage of blastocysts and number of cells per blastocyst decreased significantly in oocytes from restraint-stressed mice, addition of antioxidants to IVM medium significantly improved their blastocyst development. Supplementation of cystine and cysteamine to IVM medium reduced ROS levels and aneuploidy while increasing glutathione synthesis and improving pre- and postimplantation development of oocytes from restraint-stressed mice. Furthermore, injection of the antioxidant epigallocatechin gallate into restraint-stressed mice significantly improved the blastocyst formation and postimplantation development of their oocytes. In conclusion, restraint stress at the oocyte prematuration stage impaired the developmental potential of oocytes by increasing oxidative stress and addition of antioxidants to IVM medium or maternal antioxidant injection overcame the detrimental effect of stress-induced oxidative stress. The data reported herein are helpful when making attempts to increase the chances of a successful outcome in human IVF, because restraint was applied at a stage similar to the FSH stimulation period in a human IVF program.
机译:在这项研究中,我们使用小鼠模型测试了以下假设:约束性应激会通过引起氧化应激而损害卵母细胞的发育潜能,而抗氧化剂的补充可以克服应激性氧化应激的不利影响。雌性小鼠注射马绒毛膜促性腺激素后24小时开始承受24 h的约束压力。在压力暴露结束时,杀死小鼠以恢复卵母细胞以进行体外成熟(IVM),或者注射人绒毛膜促性腺激素并与雄性小鼠关在一起以观察体内发育。通过将抗氧化剂添加到IVM培养基中进行体外测试,或在限制压力暴露之前通过母体注射在体内进行测试。确定总氧化剂和抗氧化剂状态,氧化应激指数以及活性氧(ROS)和谷胱甘肽水平的测定表明抑制应激会增加小鼠血清,卵巢和卵母细胞的氧化应激。束缚应激小鼠的卵母细胞中胚泡的百分比和每个胚泡的细胞数显着下降,而向IVM培养基中添加抗氧化剂则显着改善了胚泡的发育。向IVM培养基中添加胱氨酸和半胱胺可降低ROS水平和非整倍性,同时增加谷胱甘肽的合成并改善约束应激小鼠卵母细胞的植入前后。此外,将抗氧化剂表没食子儿茶素没食子酸酯注射入束缚应激的小鼠中可显着改善其卵母细胞的胚泡形成和植入后发育。总之,在卵母细胞过早发育阶段的束缚应激通过增加氧化应激而损害了卵母细胞的发育潜力,向IVM培养基或母体抗氧化剂注射中添加抗氧化剂克服了应激诱导的氧化应激的不利影响。当试图增加人类IVF成功结局的机会时,本文报道的数据会有所帮助,因为在人类IVF程序中,在与FSH刺激期相似的阶段施加了限制。

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