Using multielectrode arrays to investigate neurodegenerative effects of the amyloid-beta peptide.

Steven Schulte, Manuela Gries, Anne Christmann, Karl-Herbert Schäfer
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Abstract

Background: Multielectrode arrays are widely used to analyze the effects of potentially toxic compounds, as well as to evaluate neuroprotective agents upon the activity of neural networks in short- and long-term cultures. Multielectrode arrays provide a way of non-destructive analysis of spontaneous and evoked neuronal activity, allowing to model neurodegenerative diseases in vitro. Here, we provide an overview on how these devices are currently used in research on the amyloid-β peptide and its role in Alzheimer's disease, the most common neurodegenerative disorder.

Main body: Most of the studies analysed here indicate fast responses of neuronal cultures towards aggregated forms of amyloid-β, leading to increases of spike frequency and impairments of long-term potentiation. This in turn suggests that this peptide might play a crucial role in causing the typical neuronal dysfunction observed in patients with Alzheimer's disease.

Conclusions: Although the number of studies using multielectrode arrays to examine the effect of the amyloid-β peptide onto neural cultures or whole compartments is currently limited, they still show how this technique can be used to not only investigate the interneuronal communication in neural networks, but also making it possible to examine the effects onto synaptic currents. This makes multielectrode arrays a powerful tool in future research on neurodegenerative diseases.

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利用多电极阵列研究淀粉样蛋白-β肽对神经退行性病变的影响。
背景:多电极阵列被广泛用于分析潜在毒性化合物的影响,以及评估神经保护剂对短期和长期培养的神经网络活动的影响。多电极阵列提供了一种对自发和诱发神经元活动进行非破坏性分析的方法,从而可以在体外建立神经退行性疾病模型。在此,我们将概述这些设备目前是如何用于研究淀粉样蛋白-β肽及其在阿尔茨海默病(最常见的神经退行性疾病)中的作用的:本文分析的大多数研究表明,神经元培养物对淀粉样蛋白-β的聚集形式反应迅速,导致尖峰频率增加和长期延时功能受损。这反过来又表明,这种肽可能在导致阿尔茨海默病患者典型的神经元功能障碍方面起着至关重要的作用:尽管目前使用多电极阵列来研究淀粉样β肽对神经培养物或整个区室的影响的研究数量有限,但这些研究仍然表明,这种技术不仅可以用来研究神经网络中的神经元间通信,还可以用来研究对突触电流的影响。这使得多电极阵列成为未来研究神经退行性疾病的有力工具。
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来源期刊
CiteScore
6.90
自引率
0.00%
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0
审稿时长
8 weeks
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