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小鼠胚胎暴露于活性氧后的植入前胚胎毒性。

Preimplantation embryotoxicity after mouse embryo exposition to reactive oxygen species.

作者信息

Cebral Elisa, Carrasco Isabel, Vantman David, Smith Rosita

机构信息

Instituto de Investigaciones Materno-Infantil, Hospital Clínico Materno-Infantil San Borja-Arriarán, Facultad de Medicina, Universidad de Chile, Santa Rosa 1234, Santiago, Chile.

出版信息

Biocell. 2007;31(1):51-9.

Abstract

Exposure of either gametes or embryos to conditions and/or factors that generate oxidative stress has been associated with impaired early embryogenesis. The effects of reactive oxygen species (ROS) on mouse preimplantation development, depending of the ROS-concentration and time of exposition, were studied. Two-cell embryos were incubated with 5, 10, 25 and 50 microM of hydrogen peroxide (H2O2) for 30 and 60 minutes of exposition and allowed to develop for 72 h to study the quality of development. The incubation with 50 microM H2O2 for 30 or 60 minutes, strongly inhibited the 2-cell embryo development as compared to the control (p < 0.001). Twenty-five microM H2O2 produced inhibition of blastocyst formation (p < 0.001) and 10 microM H2O2 significantly decreased the percentages of expanded and hatched blastocysts, which resulted morphologically altered (p < 0.05 and p < 0.01, respectively). The higher H2O2 concentrations were able to elicit necrotic morphology in the 2-cell arrested embryos, while 10 microM H2O2 induced moderate damage with the arrested embryos partially fragmented. In conclusion, important causes for defective preimplantation development and for early embryo losses may be due to oxidative stress because early mouse embryos exposed to ROS for short times arrested at the first cellular cycle (2-cell) and/or impaired embryo differentiation and morphogenesis, being these effects ROS-concentration-dependent.

摘要

配子或胚胎暴露于产生氧化应激的条件和/或因素下,与早期胚胎发育受损有关。研究了活性氧(ROS)对小鼠植入前发育的影响,该影响取决于ROS浓度和暴露时间。将二细胞胚胎与5、10、25和50微摩尔的过氧化氢(H2O2)孵育30和60分钟,然后让其发育72小时以研究发育质量。与对照组相比,用50微摩尔H2O2孵育30或60分钟强烈抑制了二细胞胚胎的发育(p < 0.001)。25微摩尔H2O2抑制了囊胚形成(p < 0.001),10微摩尔H2O2显著降低了扩张囊胚和孵化囊胚的百分比,导致形态改变(分别为p < 0.05和p < 0.01)。较高浓度的H2O2能够在停滞于二细胞阶段的胚胎中引发坏死形态,而10微摩尔H2O2诱导中等程度的损伤,使停滞的胚胎部分碎片化。总之,植入前发育缺陷和早期胚胎丢失的重要原因可能是氧化应激,因为短时间暴露于ROS的早期小鼠胚胎会停滞在第一个细胞周期(二细胞期)和/或损害胚胎分化和形态发生,这些影响是ROS浓度依赖性的。

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