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Catalase addition to vitrification solutions maintains goat ovarian preantral follicles stability

机译:在玻璃化溶液中添加过氧化氢酶可维持山羊卵巢窦前卵泡的稳定性

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The aim of this study was to verify whether the addition of catalase (20 IU/mL) at different steps of goat ovarian tissue vitrification affects ROS levels, follicular morphology and viability, stromal cell density, apoptosis and the expression of proteins related to DNA-damage signaling (gamma H2AX) and repair (53BP1). Goat ovarian tissues were analyzed fresh (control) or after vitrification: without catalase (VS-/WS-), with catalase in vitrification solutions (VS+/WS-), with catalase in washing solutions (VS-/WS+) or with catalase in both solutions (VS+/WS+). The vitrification without catalase had higher ROS levels than the control. The catalase, regardless the step of addition, maintained ROS levels similar to the control. There were no difference between treatments regarding follicular viability, stromal cell density and detection of gamma H2AX and 53BP1. There was no difference in follicular morphology and DNA fragmentation between groups vitrified. In conclusion, catalase addition to vitrification solutions prevents ROS formation in cryopreserved goat ovarian tissues
机译:这项研究的目的是验证在山羊卵巢组织玻璃化的不同步骤中添加过氧化氢酶(20 IU / mL)是否会影响ROS水平,卵泡形态和生存力,基质细胞密度,细胞凋亡以及与DNA-有关的蛋白质的表达损坏信号(γH2AX)和修复(53BP1)。对新鲜(对照)或玻璃化后的山羊卵巢组织进行了分析:不使用过氧化氢酶(VS- / WS-),不使用过氧化氢酶的玻璃化溶液(VS + / WS-),不使用过氧化氢酶的洗涤溶液(VS- / WS +)或不使用过氧化氢酶的玻璃化粪便。两种解决方案(VS + / WS +)。没有过氧化氢酶的玻璃化具有比对照更高的ROS水平。不管添加步骤如何,过氧化氢酶都保持与对照相似的ROS水平。在滤泡生存力,基质细胞密度和γH2AX和53BP1检测方面,治疗之间没有差异。玻璃化组之间的卵泡形态和DNA片段没有差异。总之,在玻璃化溶液中添加过氧化氢酶可防止冷冻保存的山羊卵巢组织中形成ROS

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