| Literature DB >> 27645800 |
Maria do Carmo Costa1, Naila S Ashraf1, Svetlana Fischer1, Yemen Yang1, Emily Schapka1, Gnanada Joshi2, Thomas J McQuade3, Rahil M Dharia1, Mark Dulchavsky1, Michelle Ouyang1, David Cook1, Duxin Sun4, Martha J Larsen3, Jason E Gestwicki5, Sokol V Todi2,6, Magdalena I Ivanova1,7, Henry L Paulson1.
Abstract
No disease-modifying treatment exists for the fatal neurodegenerative polyglutamine disease known both as Machado-Joseph disease and spinocerebellar ataxia type 3. As a potential route to therapy, we identified small molecules that reduce levels of the mutant disease protein, ATXN3. Screens of a small molecule collection, including 1250 Food and Drug Administration-approved drugs, in a novel cell-based assay, followed by secondary screens in brain slice cultures from transgenic mice expressing the human disease gene, identified the atypical antipsychotic aripiprazole as one of the hits. Aripiprazole increased longevity in a Drosophila model of Machado-Joseph disease and effectively reduced aggregated ATXN3 species in flies and in brains of transgenic mice treated for 10 days. The aripiprazole-mediated decrease in ATXN3 abundance may reflect a complex response culminating in the modulation of specific components of cellular protein homeostasis. Aripiprazole represents a potentially promising therapeutic drug for Machado-Joseph disease and possibly other neurological proteinopathies.Entities:
Keywords: Machado-Joseph disease; drug screen; neurodegeneration; spinocerebellar ataxia type 3; therapeutics
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Year: 2016 PMID: 27645800 PMCID: PMC5840879 DOI: 10.1093/brain/aww228
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501