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Estradiol Activates PI3K/Akt/GSK3 Pathway Under Chronic Neurodegenerative Conditions Triggered by Perinatal Asphyxia

机译:在围产期窒息引发的慢性神经变性条件下,雌二醇激活PI3K / Akt / GSK3途径

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摘要

Perinatal asphyxia (PA) remains as one of the most important causes of short-term mortality, psychiatric and neurological disorders in children, without an effective treatment. In previous studies we have observed that the expression of different neurodegenerative markers increases in CA1 hippocampal area of 4-months-old male rats born by cesarean section and exposed for 19 min to PA. We have also shown that a late treatment with 17β estradiol (daily dose of 250 μg/kg for 3 days) was able to revert the brain alterations observed in those animals. Based on these previous results, the main aim of the present study was to explore the mechanism by which the estrogenic treatment is involved in the reversion of the chronic neurodegenerative conditions induced by PA. We demonstrated that estradiol treatment of adult PA exposed animals induced an increase in estrogen receptor (ER) α and insulin-like growth factor receptor (IGF-1R) protein levels, an activation of the phosphatidylinositol 3-kinase/Akt/glycogen synthase kinase 3 beta/β-catenin signaling pathway and an increase in Bcl-2/Bax ratio in the hippocampus in comparison to PA exposed animals treated with vehicle. Taking together, our data suggest that the interaction between ERα and IGF-IR, with the subsequent downstream activation, underlies the beneficial effects of estradiol observed in late treatment of PA.
机译:围产期窒息(PA)仍然是儿童短期死亡,精神病和神经疾病的最重要原因之一,没有有效的治疗方法。在先前的研究中,我们观察到在剖腹产并暴露于PA 19分钟的4个月大雄性大鼠的CA1海马区中,不同的神经变性标记的表达增加。我们还表明,用17β雌二醇进行后期治疗(每日剂量为250μg/ kg,连续3天)能够逆转在这些动物中观察到的大脑变化。基于这些先前的结果,本研究的主要目的是探讨雌激素治疗参与由PA诱导的慢性神经退行性疾病的逆转的机制。我们证明,雌二醇治疗成年PA暴露的动物会导致雌激素受体(ER)α和胰岛素样生长因子受体(IGF-1R)蛋白水平增加,磷脂酰肌醇3-激酶/ Akt /糖原合酶激酶3的激活与用媒介物处理过的PA暴露动物相比,β/β-catenin信号通路和海马Bcl-2 / Bax比值增加。综上所述,我们的数据表明,ERα和IGF-IR之间的相互作用以及随后的下游活化是在PA晚期治疗中观察到的雌二醇的有益作用的基础。

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