神经突
海马结构
体内
莫里斯水上航行任务
神经科学
转基因小鼠
药理学
离体
海马体
淀粉样前体蛋白
阿尔茨海默病
淀粉样蛋白(真菌学)
体外
医学
生物
转基因
疾病
病理
生物化学
生物技术
基因
作者
Christophe Rochais,Cédric Lecoutey,Katia Hamidouche,Patrizia Giannoni,Florence Gaven,Eleazere Cem,Serge Mignani,Kévin Baranger,Thomas Fréret,Joël Bockaert,Santiago Rivera,Michel Boulouard,Patrick Dallemagne,Sylvie Claeysen
摘要
Background and Purpose We recently identified donecopride as a pleiotropic compound able to inhibit AChE and to activate 5‐HT 4 receptors. Here, we have assessed the potential therapeutic effects of donecopride in treating Alzheimer's disease (AD). Experimental Approach We used two in vivo animal models of AD, transgenic 5XFAD mice and mice exposed to soluble amyloid‐β peptides and, in vitro, primary cultures of rat hippocampal neurons. Pro‐cognitive and anti‐amnesic effects were evaluated with novel object recognition, Y‐maze, and Morris water maze tests. Amyloid load in mouse brain was measured ex vivo and effects of soluble amyloid‐β peptides on neuronal survival and neurite formation determined in vitro. Key Results In vivo, chronic (3 months) administration of donecopride displayed potent anti‐amnesic properties in the two mouse models of AD, preserving learning capacities, including working and long‐term spatial memories. These behavioural effects were accompanied by decreased amyloid aggregation in the brain of 5XFAD mice and, in cultures of rat hippocampal neurons, reduced tau hyperphosphorylation. In vitro, donecopride increased survival in neuronal cultures exposed to soluble amyloid‐β peptides, improved the neurite network and provided neurotrophic benefits, expressed as the formation of new synapses. Conclusions and Implications Donecopride acts like a Swiss army knife, exhibiting a range of sustainable symptomatic therapeutic effects and potential disease‐modifying effects in models of AD. Clinical trials with this promising drug candidate will soon be undertaken to confirm its therapeutic potential in humans.
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