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首页> 外文期刊>Journal of neurobiology >Chronic exposure to ethanol alters neurotrophin content in the basal forebrain-cortex system in the mature rat: Effects on autocrine-paracrine mechanisms.
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Chronic exposure to ethanol alters neurotrophin content in the basal forebrain-cortex system in the mature rat: Effects on autocrine-paracrine mechanisms.

机译:长期暴露于乙醇会改变成熟大鼠基底前脑皮质系统中的神经营养蛋白含量:对自分泌-旁分泌机制的影响。

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摘要

Neurotrophins are broadly expressed in the mammalian forebrain: notably in cerebral cortex and the basal forebrain (e.g., the septal and basal nuclei). These factors promote neuronal survival and plasticity, and have been implicated as key players in learning and memory. Chronic exposure to ethanol causes learning and memory deficits. We tested the hypothesis that ethanol affects neurotrophin expression and predicted that these changes would be consistent with alterations in retrograde or autocrine/paracrine systems. Mature rats were fed a liquid diet containing ethanol daily for 8 or 24 weeks. Weight-matched controls were pair-fed an isocaloric, isonutritive diet. Proteins from five structures (parietal and entorhinal cortices, hippocampus, and the basal and septal nuclei) were studied. ELISAs were used to determine the concentration of nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and neurotrophin-3 (NT-3). All three neurotrophins were detected in each structure examined. Ethanol treatment significantly (p < 0.05) affected neurotrophin expression in time- and space-dependent manners. NGF content was generally depressed by ethanol exposure, whereas NT-3 content increased. BDNF concentration was differentially affected by ethanol: it increased in the parietal cortex and the basal forebrain and decreased in the hippocampus. With the exception of NGF in the septohippocampal system, the ethanol-induced changes in connected structures were inconsistent with changes that would be predicted from a retrograde model. Thus, the present data (a) support the concept that neurotrophins act through a nonretrograde system (i.e., a local autocrine/paracrine system), and (b) that chronic exposure to ethanol disrupts these regulatory mechanisms. Copyright 2004 Wiley Periodicals, Inc. J Neurobiol 60: 490-498, 2004
机译:神经营养蛋白在哺乳动物的前脑中广泛表达:特别是在大脑皮层和基底前脑(例如中隔和基底核)中。这些因素促进了神经元的生存和可塑性,并被认为是学习和记忆的关键因素。长期暴露于乙醇会导致学习和记忆障碍。我们测试了乙醇影响神经营养蛋白表达的假设,并预测这些变化将与逆行或自分泌/旁分泌系统的改变一致。给成年大鼠每天喂含乙醇的流质饮食,持续8或24周。与体重匹配的对照组配对喂养等热量,等营养的饮食。研究了来自五个结构(顶叶和内嗅皮层,海马以及基底和中隔核)的蛋白质。 ELISA用于确定神经生长因子(NGF),脑源性神经营养因子(BDNF)和Neurotrophin-3(NT-3)的浓度。在所检查的每个结构中均检测到所有三种神经营养蛋白。乙醇处理以时间和空间依赖性方式显着(p <0.05)影响神经营养蛋白的表达。 NGF含量通常因乙醇暴露而降低,而NT-3含量增加。 BDNF浓度受乙醇的影响不同:乙醇在顶叶皮质和基底前脑中升高,在海马中降低。除了海马体系统中的NGF以外,乙醇诱导的连接结构变化与逆行模型预测的变化不一致。因此,本数据(a)支持神经营养蛋白通过不可逆系统(即局部自分泌/旁分泌系统)起作用的概念,以及(b)长期暴露于乙醇破坏了这些调节机制。版权所有2004 Wiley Periodicals,Inc. J Neurobiol 60:490-498,2004

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