Valencia Martina, Santander Odra, Torres Eloísa, Zamora Natali, Muñoz Fernanda, Pascual Rodrigo
Laboratorio de Neurociencias. Escuela de Kinesiología. Pontificia Universidad de Valparaíso, Chile.
Avenida Universidad #330, Valparaíso., 2340000, Chile.
AIMS Neurosci. 2022 Jul 14;9(3):320-344. doi: 10.3934/Neuroscience.2022018. eCollection 2022.
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.
在产前阶段,接触合成糖皮质激素(SGCs)会改变胎儿的正常发育,导致日后患病。此前,我们已经表明,产前接触糖皮质激素的青春期大鼠后代的浦肯野细胞树突细胞结构会发生改变。然而,这些改变背后的分子机制仍不清楚。一种可能的分子候选物,其失调可能是这些变化的基础,是糖皮质激素受体(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),它特异性地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会受到子宫内接触合成糖皮质激素的影响。因此,本研究的第一个目标是通过免疫组织化学和蛋白质印迹技术,在相当于青春期的出生后阶段(出生后第52天)评估后代,来评估GR、NT-3和TrkC在小脑蚓部的表达。此外,我们使用高架十字迷宫和埋珠试验评估后代的焦虑样行为。另外,环境富集(EE)可以增加一些神经营养因子的表达并具有抗焦虑作用。因此,我们想评估EE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:i)产前给予倍他米松(BET)会降低小脑蚓部GR、NT-3和TrkC的表达;ii)产前给予BET会降低小脑半球GR的表达;iii)增强同一后代的焦虑样行为;iv)接触EE可逆转小脑蚓部GR、NT-3和TrkC表达的降低;v)减少焦虑样行为。总之,断奶后18天应用富集环境能够使产前暴露于倍他米松的青春期大鼠的GR、NT-3和TrkC表达水平重新稳定,并逆转观察到的焦虑行为。