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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >The effects of ovariectomy and estrogen replacement on trkA and choline acetyltransferase mRNA expression in the basal forebrain of the adult female Sprague-Dawley rat.
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The effects of ovariectomy and estrogen replacement on trkA and choline acetyltransferase mRNA expression in the basal forebrain of the adult female Sprague-Dawley rat.

机译:卵巢切除和雌激素替代对成年雌性Sprague-Dawley大鼠基底前脑trkA和胆碱乙酰转移酶mRNA表达的影响。

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摘要

Cognitive deficits associated with aging and with neurodegenerative diseases such as Alzheimer's disease have been attributed to degeneration of cholinergic neurons in the basal forebrain. Estrogen is known to provide trophic support to cholinergic neurons, although the mechanisms underlying the actions of estrogen have yet to be determined. Because cholinergic neurons require neurotrophic growth factors for their survival, it is possible that the trophic effects of estrogen on basal forebrain systems are caused by enhanced expression of neurotrophins or their receptors. To begin to examine this hypothesis, we used in situ hybridization analysis to determine the effects of ovariectomy (ovx) and estrogen replacement on trkA mRNA levels in the rat basal forebrain. Ten days of estrogen deprivation after ovx resulted in significant decreases in trkA mRNA levels in the horizontal limb of the diagonal band of Broca and the nucleus basalis of Meynert. Short-term estrogen replacement therapy restored trkA mRNAexpression to a level comparable with ovary-intact animals. No changes in trkA mRNA levels were observed in the vertical limb of the diagonal band of Broca after ovx or estrogen replacement. To assess the functional status of cholinergic neurons in the absence and presence of estrogen, the effects of ovx and estrogen replacement on ChAT mRNA levels were also examined and found to reflect the changes observed in trkA mRNA expression. These studies suggest that the trophic effects of estrogen on basal forebrain cholinergic systems may be mediated, in part, through the signaling of neurotrophic growth factors through their receptors.
机译:与衰老和神经退行性疾病(例如阿尔茨海默氏病)相关的认知缺陷已归因于基底前脑中胆碱能神经元的变性。尽管尚未确定雌激素作用的基本机制,但已知雌激素可为胆碱能神经元提供营养支持。因为胆碱能神经元的生存需要神经营养生长因子,所以雌激素对基础前脑系统的营养作用可能是由于神经营养蛋白或其受体的表达增强所致。为了检查这一假设,我们使用原位杂交分析来确定卵巢切除术(ovx)和雌激素替代对大鼠基底前脑trkA mRNA水平的影响。 ovx后剥夺十天的雌激素会导致Broca对角带水平臂和Meynert基底核的trkA mRNA水平显着下降。短期雌激素替代疗法可将trkA mRNA表达恢复至与卵巢完整动物相当的水平。 ovx或雌激素置换后,在Broca对角带的垂直分支中未观察到trkA mRNA水平的变化。为了评估在不存在雌激素的情况下胆碱能神经元的功能状态,还检查了ovx和雌激素替代对ChAT mRNA水平的影响,发现该反应反映了trkA mRNA表达的变化。这些研究表明,雌激素对基底前脑胆碱能系统的营养作用可能部分地通过其受体的神经营养生长因子的信号传导来介导。

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