环境富集逆转由产前暴露于合成糖皮质激素引起的小脑损伤。

IF 3.1 Q2 NEUROSCIENCES
AIMS Neuroscience Pub Date : 2022-07-14 eCollection Date: 2022-01-01 DOI:10.3934/Neuroscience.2022018
Martina Valencia, Odra Santander, Eloísa Torres, Natali Zamora, Fernanda Muñoz, Rodrigo Pascual
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引用次数: 1

摘要

在产前生活中,暴露于合成糖皮质激素(SGCs)可改变胎儿的正常发育,导致生命后期的疾病。在此之前,我们已经证明了青春期大鼠后代在产前暴露于糖皮质激素时浦肯野细胞树突状细胞结构的改变。然而,这些改变背后的分子机制尚不清楚。糖皮质激素受体(GR)和神经营养因子3/原肌球蛋白受体激酶C,神经营养复合物(NT-3/TrkC)可能是这些变化的潜在分子,其特异性调节小脑蚓部神经元连接的发育。迄今为止,没有证据表明这种神经营养复合物的小脑表达水平受到子宫内暴露于合成糖皮质激素的影响。因此,本研究的第一个目的是利用免疫组织化学和western blot技术,通过评估出生后相当于青春期(出生后52天)的后代,评估GR、NT-3和TrkC在小脑蚓中的表达。此外,我们还使用高架迷宫和大理石掩埋测试来评估后代的焦虑样行为。此外,环境富集(EE)可增加某些神经营养因子的表达,具有抗焦虑作用。因此,我们想评估情感表达是否能逆转产前倍他米松暴露引起的长期改变。本研究的主要发现如下:1)产前给药倍他米松(betamethasone, BET)降低了小脑蚓部GR、NT-3和TrkC的表达;2)产前给药倍他米松(betamethasone, BET)降低了小脑半球GR的表达,3)增加了同一子代的焦虑样行为;4)EE暴露逆转了小脑蚓部GR、NT-3和TrkC的表达减少,5)减少了焦虑样行为。综上所述,断奶后18天的强化环境能够重新稳定GR、NT-3和TrkC的表达水平,并逆转青春期大鼠产前暴露于倍他米松的焦虑行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Environmental enrichment reverses cerebellar impairments caused by prenatal exposure to a synthetic glucocorticoid.

Environmental enrichment reverses cerebellar impairments caused by prenatal exposure to a synthetic glucocorticoid.

Environmental enrichment reverses cerebellar impairments caused by prenatal exposure to a synthetic glucocorticoid.

Environmental enrichment reverses cerebellar impairments caused by prenatal exposure to a synthetic glucocorticoid.

During prenatal life, exposure to synthetic glucocorticoids (SGCs) can alter normal foetal development, resulting in disease later in life. Previously, we have shown alterations in the dendritic cytoarchitecture of Purkinje cells in adolescent rat progeny prenatally exposed to glucocorticoids. However, the molecular mechanisms underlying these alterations remain unclear. A possible molecular candidate whose deregulation may underlie these changes is the glucocorticoid receptor (GR) and neurotrophin 3/ tropomyosin receptor kinase C, neurotrophic complex (NT-3/TrkC), which specifically modulates the development of the neuronal connections in the cerebellar vermis. To date, no evidence has shown that the cerebellar expression levels of this neurotrophic complex are affected by exposure to a synthetic glucocorticoid in utero. Therefore, the first objective of this investigation was to evaluate the expression of GR, NT-3 and TrkC in the cerebellar vermis using immunohistochemistry and western blot techniques by evaluating the progeny during the postnatal stage equivalent to adolescence (postnatal Day 52). Additionally, we evaluated anxiety-like behaviours in progeny using the elevated plus maze and the marble burying test. In addition, an environmental enrichment (EE) can increase the expression of some neurotrophins and has anxiolytic power. Therefore, we wanted to assess whether an EE reversed the long-term alterations induced by prenatal betamethasone exposure. The major findings of this study were as follows: i) prenatal betamethasone (BET) administration decreases GR, NT-3 and TrkC expression in the cerebellar vermis ii) prenatal BET administration decreases GR expression in the cerebellar hemispheres and iii) enhances the anxiety-like behaviours in the same progeny, and iv) exposure to an EE reverses the reduced expression of GR, NT-3 and TrkC in the cerebellar vermis and v) decreases anxiety-like behaviours. In conclusion, an enriched environment applied 18 days post-weaning was able to restabilize GR, NT-3 and TrkC expression levels and reverse anxious behaviours observed in adolescent rats prenatally exposed to betamethasone.

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来源期刊
AIMS Neuroscience
AIMS Neuroscience NEUROSCIENCES-
CiteScore
4.20
自引率
0.00%
发文量
26
审稿时长
8 weeks
期刊介绍: AIMS Neuroscience is an international Open Access journal devoted to publishing peer-reviewed, high quality, original papers from all areas in the field of neuroscience. The primary focus is to provide a forum in which to expedite the speed with which theoretical neuroscience progresses toward generating testable hypotheses. In the presence of current and developing technology that offers unprecedented access to functions of the nervous system at all levels, the journal is designed to serve the role of providing the widest variety of the best theoretical views leading to suggested studies. Single blind peer review is provided for all articles and commentaries.
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