首页> 外文期刊>Journal of Animal Science >Alpha-linolenic acid treatment during oocyte maturation enhances embryonic development by influencing mitogen-activated protein kinase activity and intraoocyte glutathione content in pigs
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Alpha-linolenic acid treatment during oocyte maturation enhances embryonic development by influencing mitogen-activated protein kinase activity and intraoocyte glutathione content in pigs

机译:卵母细胞成熟期间的α-亚麻酸治疗通过影响猪中的丝裂剂活化的蛋白激酶活性和猪中的胃癌谷胱甘肽含量来增强胚胎发育

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The purpose of this study was to examine the effects of alpha-linolenic acid (ALA) treatment during in vitro maturation (IVM) on nuclear maturation, intraoocyte glutathione (GSH) content, meiotic progression, and developmental competence after parthenogenesis (PA) and somatic cell nuclear transfer (SCNT) in pigs. Medium-199 containing 10% (vol/vol) porcine follicular fluid (PFF; PPF control) or 0.4% (wt/vol) fatty acid-free BSA (BSA control) was used for IVM. The proportion of oocytes reaching the metaphase II (MII) stage was not influenced by ALA treatment at various concentrations (50, 100, and 200 mu M). However, treatment with 100 mu M ALA significantly increased (P 0.05) intraoocyte GSH content (1.19 vs. 1.00 and 0.92 pixels per oocyte, comparing the treated oocytes, BSA control, and PFF control, respectively) and embryonic development to the blastocyst stage after PA (47.1 vs. 35.5 and 35.2%) and SCNT (31.4 vs. 23.9 and 24.3%). ALA treatment (100 mu M) accelerated oocyte maturation, and a higher proportion of ALA-treated oocytes (89.6%) reached the MII stage than did the untreated controls (75.5%) at 33 h of IVM. Mitogen-activated protein kinase kinase inhibitor (U0126) treatment during IVM inhibited nuclear maturation and embryonic development after PA. However, 100 mu M ALA completely counteracted the suppressive effect of U0126 on nuclear maturation and partially counteracted the effect on blastocyst formation. Our results demonstrate that treatment with 100 mu M ALA during IVM improves developmental competence by accelerating nuclear maturation and also influencing cytoplasmic maturation, such as increased GSH content in IVM oocytes.
机译:本研究的目的是检测在核成熟(IVM)期间α-亚麻酸(ALA)治疗对核成熟,介性谷胱甘肽(GSH)含量,减数分裂进展和发育能力后的核成熟(PA)和体细胞猪细胞核转移(SCNT)。含有10%(Vol / Vol)猪卵泡液(PPF控制)或0.4%(WT / VOL)脂肪酸BSA(BSA对照)的中等-19用于IVM。到达中期II(MII)阶段的卵母细胞的比例不受各种浓度(50,100和200μm)的ALA处理的影响。然而,用100μmAla的治疗显着增加(p <0.05)内胃癌GSH含量(每卵母细胞的1.19与1.00和0.92像素,分别将处理的卵母细胞,BSA对照和PFF控制分别与胚泡发育进行比较PA(47.1与35.5和35.2%)和SCNT(31.4与23.9和24.3%)的阶段。 ALA治疗(100μm)加速卵母细胞成熟,较高比例的ALA处理的卵母细胞(89.6%)达到MII阶段,而不是IVM的33小时的未处理对照(75.5%)。丝裂剂激活蛋白激酶激酶抑制剂(U0126)在IVM期间治疗抑制PA后的核成熟和胚胎发育。然而,100 mu m Ala完全抵消了U0126对核成熟的抑制作用,并部分地抵消了对胚泡形成的影响。我们的结果表明,IVM期间100 mu M ALA的治疗通过加速核成熟并影响细胞质成熟,例如细胞质成熟,例如IVM卵母细胞中的GSH含量增加,提高了发育能力。

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