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Effect of di-(2-ethylhexyl) phthalate and mono-(2-ethylhexyl) phthalate on in vitro developmental competence of bovine oocytes

机译:邻苯二甲酸二(2-乙基己基)酯和邻苯二甲酸单(2-乙基己基)酯对牛卵母细胞体外发育能力的影响

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In the last decade, potential exposure of humans and animals to industrial chemicals and pesticides has been a growing concern. In the present study, di-(2-ethylhexyl) phthalate (DEHP) and mono-(2-ethylhexyl) phthalate (MEHP) were used to model the effects of endocrine-disrupting compounds and their risk in relation to early embryonic losses. Exposure of cumulus oocyte complexes during maturation to 50 micro M MEHP reduced the proportion of oocytes that underwent nuclear maturation (p<0.05) and increased the proportion of apoptotic oocytes (p<0.05). Furthermore, phthalates reduced cleavage rate in the MEHP-treated group (p<0.05) and the proportion of embryos developing to the blastocyst stage in both DEHP- and MEHP-treated groups (p<0.05). The total cell count for blastocysts developing from MEHP-treated oocytes was lower than in controls (p<0.05). Exposure of oocytes to MEHP during maturation reduced (p<0.05) the expression of ASAH1 (an anti-apoptotic factor), CCNA2 (involved in cell cycle control), and POU5F1 (responsible for pluripotency) in matured oocytes. Furthermore, the reduced mRNA expression of POU5F1 and ASAH1 lasted into two-cell stage embryos (p<0.05). Phthalate-induced alterations in POU5F1, ASAH1, and CCNA2 expression might explain in part the reduced developmental competence of MEHP-treated oocytes.Digital Object Identifier http://dx.doi.org/10.1007/s10565-012-9230-1
机译:在过去的十年中,人类和动物对工业化学药品和杀虫剂的潜在暴露日益引起人们的关注。在本研究中,邻苯二甲酸二(2-乙基己基)酯(DEHP)和邻苯二甲酸单(2-乙基己基)酯(MEHP)被用来模拟干扰内分泌的化合物的作用及其与早期胚胎损失有关的风险。成熟期间卵丘卵母细胞复合物暴露于50 micro M MEHP会降低经历核成熟的卵母细胞比例(p <0.05),并增加凋亡卵母细胞的比例(p <0.05)。此外,在DEHP和MEHP处理组中,邻苯二甲酸盐均降低了MEHP处理组的卵裂率(p <0.05)和发育到胚泡期的胚胎比例(p <0.05)。由MEHP处理的卵母细胞发育的胚泡的总细胞数低于对照组(p <0.05)。在成熟过程中,卵母细胞暴露于MEHP可降低(p <0.05)ASAH1(抗凋亡因子),CCNA2(参与细胞周期控制)和POU5F1(负责多能性)在成熟卵母细胞中的表达。此外,POU5F1和ASAH1的mRNA表达降低持续到两细胞期胚胎中(p <0.05)。邻苯二甲酸酯诱导的POU5F1,ASAH1和CCNA2表达的改变可能部分解释了MEHP处理的卵母细胞发育能力降低。数字对象标识符http://dx.doi.org/10.1007/s10565-012-9230-1

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