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• W1974323467 abstract "Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and is the most common form of dementia in elderly people. The accumulation of amyloid β (Aβ) is one of the histopathological hallmarks of AD. Aβ is aggregated to form oligomers which are toxic to neurons and are critical to the onset and progression of AD. In a Caenorhabditis elegans (C. elegans) model of AD, human Aβ is expressed intracellularly in the body wall muscle. The expression and subsequent aggregation of Aβ in the muscle lead to progressive paralysis. Although the mechanism of action is unknown, antidepressants have been used with FDA approved drugs for dementia in AD and have been shown to enhance cognitive function in human and in animal models of AD. We found that the antidepressant fluoxetine, a selective serotonin reuptake inhibitor, significantly delayed Aβ-induced paralysis in the C. elegans model of Aβ toxicity by reducing Aβ oligomers. Our results showed that insulin signaling and DAF-16/FOXO transcription factors were required for fluoxetine-mediated delayed paralysis. We also found that fluoxetine increased thermal stress resistance and extended life span. These findings suggests that fluoxetine may have benefit for the treatment of AD by the reduction of proteotoxicity." @default.
• W1974323467 created "2016-06-24" @default.
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• W1974323467 date "2010-09-01" @default.
• W1974323467 modified "2023-10-16" @default.
• W1974323467 title "Fluoxetine protects against amyloid-beta toxicity, in part via daf-16 mediated cell signaling pathway, in Caenorhabditis elegans" @default.
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• W1974323467 doi "https://doi.org/10.1016/j.neuropharm.2010.04.008" @default.
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