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微管稳定剂多西他赛和紫杉醇可减少纺锤体损伤,并在玻璃化过程中维持体外成熟牛卵母细胞的发育能力。

Microtubule stabilisers docetaxel and paclitaxel reduce spindle damage and maintain the developmental competence of in vitro-mature bovine oocytes during vitrification.

作者信息

Pitchayapipatkul Jakkhaphan, Somfai Tamás, Matoba Satoko, Parnpai Rangsan, Nagai Takashi, Geshi Masaya, Vongpralub Thevin

机构信息

Faculty of Agriculture, Princess of Naradhiwas University, Narathiwat 96000, Thailand.

Animal Breeding and Reproduction Research Division, National Agriculture and Food Research Organisation (NARO) Institute of Livestock and Grassland Science, 2 Ikenodai, Tsukuba, Ibaraki 305-0901, Japan.

出版信息

Reprod Fertil Dev. 2017 Sep;29(10):2028-2039. doi: 10.1071/RD16193.

Abstract

This study compared the efficacy of docetaxel (DT) and paclitaxel (PT) in reducing spindle damage during vitrification and maintaining the developmental competence of in vitro-matured (IVM) bovine oocytes after vitrification and warming. Pretreatment of IVM oocytes with 0.05µM DT for 30min before vitrification resulted in significantly higher (P<0.05) rates of oocyte survival and cleavage after IVF, as well as subsequent blastocyst rates on Days 7-9 and hatching on Days 8-9, compared with oocytes pretreated with 1.0µM PT before vitrification or those vitrified without pretreatment. When nuclear status and spindle morphology of vitrified oocytes were assess after warming by immunostaining, DT pretreatment before vitrification resulted in a significantly higher (P<0.05) percentage of oocytes at the MII stage with a normal, intact spindle compared with PT pretreatment or no pretreatment, but the percentage of MII oocytes was still significantly lower (P<0.05) than in the control group. Pretreatment of IVM bovine oocytes with 0.05µM DT or 1.0µM PT for 30min before vitrification reduces spindle damage to the same extent, without side effects on fertilisation and development. Pretreatment with 0.05µM DT improved the developmental competence of vitrified-warmed oocytes to a greater degree than 1.0µM PT pretreatment.

摘要

本研究比较了多西他赛(DT)和紫杉醇(PT)在玻璃化冷冻过程中减少纺锤体损伤以及维持玻璃化冷冻和复温后体外成熟(IVM)牛卵母细胞发育能力方面的效果。与玻璃化冷冻前用1.0µM PT预处理的卵母细胞或未预处理直接玻璃化冷冻的卵母细胞相比,玻璃化冷冻前用0.05µM DT对IVM卵母细胞预处理30分钟,可使体外受精后卵母细胞的存活和分裂率显著更高(P<0.05),以及在第7 - 9天的囊胚率和第8 - 9天的孵化率也更高。通过免疫染色在复温后评估玻璃化冷冻卵母细胞的核状态和纺锤体形态时,玻璃化冷冻前DT预处理导致处于MII期且纺锤体正常、完整的卵母细胞百分比显著高于PT预处理组或未预处理组(P<0.05),但MII期卵母细胞的百分比仍显著低于对照组(P<0.05)。玻璃化冷冻前用0.05µM DT或1.0µM PT对IVM牛卵母细胞预处理30分钟,在减少纺锤体损伤方面程度相同,且对受精和发育无副作用。与1.0µM PT预处理相比,0.05µM DT预处理能更大程度地提高玻璃化冷冻 - 复温卵母细胞的发育能力。

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