Galantamine improves olfactory learning in the Ts65Dn mouse model of Down syndrome

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作者
Fabio M. Simoes de Souza
Nicolas Busquet
Megan Blatner
Kenneth N. Maclean
Diego Restrepo
机构
[1] Cell and Developmental Biology,Department of Pediatrics
[2] School of Medicine,undefined
[3] University of Colorado Anschutz Medical Campus,undefined
[4] University of Colorado Denver,undefined
[5] School of Medicine,undefined
[6] University of Colorado Anschutz Medical Campus,undefined
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Scientific Reports | / 1卷
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摘要
Down syndrome (DS) is the most common form of congenital intellectual disability. Although DS involves multiple disturbances in various tissues, there is little doubt that in terms of quality of life cognitive impairment is the most serious facet and there is no effective treatment for this aspect of the syndrome. The Ts65Dn mouse model of DS recapitulates multiple aspects of DS including cognitive impairment. Here the Ts65Dn mouse model of DS was evaluated in an associative learning paradigm based on olfactory cues. In contrast to disomic controls, trisomic mice exhibited significant deficits in olfactory learning. Treatment of trisomic mice with the acetylcholinesterase inhibitor galantamine resulted in a significant improvement in olfactory learning. Collectively, our study indicates that olfactory learning can be a sensitive tool for evaluating deficits in associative learning in mouse models of DS and that galantamine has therapeutic potential for improving cognitive abilities.
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[31]   Increased hippocampal epigenetic age in the Ts65Dn mouse model of Down Syndrome [J].
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[33]   Alterations of central noradrenergic transmission in Ts65Dn mouse, a model for Down syndrome [J].
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Vallina, IF ;
Baamonde, C ;
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Florez, J .
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[34]   Synaptic Vesicle Recycling Is Unaffected in the Ts65Dn Mouse Model of Down Syndrome [J].
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[35]   Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome [J].
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[36]   Luteolin induces hippocampal neurogenesis in the Ts65Dn mouse model of Down syndrome [J].
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[37]   Postnatal lethality and cardiac anomalies in the Ts65Dn Down Syndrome mouse model [J].
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[38]   APP accumulation and inflammation in the Ts65dn mouse, a model for Down's syndrome [J].
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[40]   Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn [J].
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