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阿尔茨海默病模型斑马鱼多巴胺释放受损和潜在学习能力下降。

Impaired Dopamine Release and Latent Learning in Alzheimer's Disease Model Zebrafish.

机构信息

Department of Chemistry and R.N. Adams Institute for Bioanalytical Chemistry, University of Kansas, Lawrence, Kansas 66045, United States.

Department of Analytical Chemistry, UNESCO Laboratory of Environmental Electrochemistry, Charles University, Prague 2 12843, Czech Republic.

出版信息

ACS Chem Neurosci. 2022 Oct 5;13(19):2924-2931. doi: 10.1021/acschemneuro.2c00484. Epub 2022 Sep 16.

DOI:10.1021/acschemneuro.2c00484
PMID:36113115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10127145/
Abstract

Alzheimer's disease (AD) is a progressive, fatal, neurodegenerative disorder for which only treatments of limited efficacy are available. Despite early mentions of dementia in the ancient literature and the first patient diagnosed in 1906, the underlying causes of AD are not well understood. This study examined the possible role of dopamine, a neurotransmitter that is involved in cognitive and motor function, in AD. We treated adult zebrafish () with okadaic acid (OKA) to model AD and assessed the resulting behavioral and neurochemical changes. We then employed a latent learning paradigm to assess cognitive and motor function followed by neurochemical analysis with fast-scan cyclic voltammetry (FSCV) at carbon fiber microelectrodes to measure the electrically stimulated dopamine release. The behavioral assay showed that OKA treatment caused fish to have lower motivation to reach the goal chamber, resulting in impeded learning and decreased locomotor activity compared to controls. Our voltammetric measurements revealed that the peak dopamine overflow in OKA-treated fish was about one-third of that measured in controls. These findings highlight the profound neurochemical changes that may occur in AD. Furthermore, they demonstrate that applying the latent learning paradigm and FSCV to zebrafish is a promising tool for future neurochemical studies and may be useful for screening drugs for the treatment of AD.

摘要

阿尔茨海默病(AD)是一种进行性、致命的神经退行性疾病,目前仅存在一些疗效有限的治疗方法。尽管在古代文献中很早就有关于痴呆的记载,并且在 1906 年首次诊断出了该病患者,但 AD 的根本病因仍不清楚。本研究探讨了一种神经递质多巴胺在 AD 中的可能作用,多巴胺参与认知和运动功能。我们用岗田酸(OKA)处理成年斑马鱼以建立 AD 模型,并评估由此产生的行为和神经化学变化。然后,我们采用潜在学习范式来评估认知和运动功能,随后使用碳纤维微电极上的快速扫描循环伏安法(FSCV)进行神经化学分析,以测量电刺激引起的多巴胺释放。行为测定表明,与对照组相比,OKA 处理会导致鱼到达目标室的动机降低,从而阻碍学习并降低运动活性。我们的伏安测量结果表明,OKA 处理组鱼的多巴胺峰溢出量约为对照组的三分之一。这些发现强调了 AD 中可能发生的深刻神经化学变化。此外,它们表明将潜在学习范式和 FSCV 应用于斑马鱼是未来神经化学研究的一种很有前途的工具,并且可能有助于筛选治疗 AD 的药物。