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Testing the critical window of estradiol replacement on gene expression of vasopressin, oxytocin, and their receptors, in the hypothalamus of aging female rats

机译:在衰老雌性大鼠的下丘脑中测试雌二醇替代对血管加压素,催产素及其受体的基因表达的关键窗口

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The current study tested the "critical window" hypothesis of menopause that postulates that the timing and duration of hormone treatment determine their potential outcomes. Our focus was genes in the rat hypothalamus involved in social and affiliative behaviors that change with aging and/or estradiol (Es): Avp, Avpr1a, Oxt, Oxtr, and Esr2 in the paraventricular nucleus (PVN) and supraoptic nucleus (SON). Rats were reproductively mature or aging adults, ovariectomized, given E-2 or vehicle treatment of different durations, with or without a post-ovariectomy delay. Our hypothesis was that age-related changes in gene expression are mitigated by E-2 treatments. Contrary to this, PVN Oxtr increased with E-2, and Avprl a increased with age. In the SON, Avprl a increased with age, Oxtr with age and timing, and Avp was altered by duration. Thus, chronological age and E-2 have independent actions on gene expression, with the "critical window" hypothesis supported by the observed timing and duration effects. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:目前的研究测试了“关键窗口”假设的绝经假设,其假设激素治疗的时序和持续时间决定了它们的潜在结果。我们的重点是大鼠下丘脑中的基因,参与了与衰老和/或雌二醇(ES)的社会和隶属度行为转化:AVP,AVPR1A,OXT,OXTR和ESR2中的椎间盘(PVN)和中学核(SON)。大鼠成熟或老化成年人,卵巢切除,给予不同持续时间的E-2或载体处理,有或没有卵巢切除术延迟。我们的假设是通过E-2治疗减轻了基因表达的年龄相关变化。与此相反,PVN OXTR随着E-2的增加,AVPRL A随着年龄而增加。在儿子中,AVPRL A随着年龄的增长而增加,随着年龄和时序,AVP被持续改变。因此,时间年龄和E-2对基因表达具有独立的作用,具有观察时间和持续时间效应的“临界窗口”假设。 (c)2015 Elsevier Ireland Ltd.保留所有权利。

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