Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/32850

TitleChronic treatment with 17-DMAG improves balance and coordination in a new mouse model of Machado-Joseph disease
Author(s)Fernandes, Anabela Silva
Silva, Sara Duarte
Carvalho, Andreia Neves
Amorim, Marina
Cunha, Carina Soares
Oliveira, Pedro
Thirstrup, Kenneth
Castro, Andreia Cristiana Teixeira de
Maciel, P.
KeywordsPolyglutamine
Animal models
Ataxia
Behavior
Therapy
Autophagy
Issue date2014
PublisherSpringer
JournalNeurotherapeutics
Abstract(s)Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disease currently with no treatment. We describe a novel mouse model of MJD which expresses mutant human ataxin-3 at near endogenous levels and manifests MJD-like motor symptoms that appear gradually and progress over time. CMVMJD135 mice show ataxin-3 intranuclear inclusions in the CNS and neurodegenerative changes in key disease regions, such as the pontine and dentate nuclei. Hsp90 inhibition has shown promising outcomes in some neurodegenerative diseases, but nothing is known about its effects in MJD. Chronic treatment of CMVMJD mice with Hsp90 inhibitor 17-DMAG resulted in a delay in the progression of their motor coordination deficits and, at 22 and 24 weeks of age, was able to rescue the uncoordination phenotype to wild-type levels; in parallel, a reduction in neuropathology was observed in treated animals. We observed limited induction of heat-shock proteins with treatment, but found evidence that 17-DMAG may be acting through autophagy, as LC3-II (both at mRNA and protein levels) and beclin-1 were induced in the brain of treated animals. This resulted in decreased levels of the mutant ataxin-3 and reduced intranuclear aggregation of this protein. Our data validate this novel mouse model as a relevant tool for the study of MJD pathogenesis and for pre-clinical studies, and show that Hsp90 inhibition is a promising therapeutic strategy for MJD.
TypeArticle
URIhttp://hdl.handle.net/1822/32850
DOI10.1007/s13311-013-0255-9
ISSN1933-7213
Publisher versionhttp://www.springer.com
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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