Literature DB >> 11150059

Motor learning in Ts65Dn mice, a model for Down syndrome.

L A Hyde1, L S Crnic, A Pollock, P C Bickford.   

Abstract

Ts65Dn mice are a genetic model for Down syndrome. Both individuals with Down syndrome and Ts65Dn mice have reduced cerebellar volumes and the cerebellum is involved in motor learning. Conflicting results have been reported on the motor learning abilities of Ts65Dn mice, which may be related to procedural differences between the motor learning tasks used in different laboratories and/or variability in phenotype because of the segregating background on which the mice are maintained. In this study, we examined learning in three types of motor tasks (peg running, accelerating rotorod, and rotating rod) which were initially easy for mice and gradually increased in difficulty. Ts65Dn mice learned the peg running task as well as controls, and learned the accelerating rotorod and rotating rod tasks as well as, and even better than, controls. These data indicate that Ts65Dn mice are not impaired in motor learning.

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Year:  2001        PMID: 11150059     DOI: 10.1002/1098-2302(2001)38:1<33::aid-dev3>3.0.co;2-0

Source DB:  PubMed          Journal:  Dev Psychobiol        ISSN: 0012-1630            Impact factor:   3.038


  21 in total

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2.  Abnormal expression of the G-protein-activated inwardly rectifying potassium channel 2 (GIRK2) in hippocampus, frontal cortex, and substantia nigra of Ts65Dn mouse: a model of Down syndrome.

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3.  Hedgehog agonist therapy corrects structural and cognitive deficits in a Down syndrome mouse model.

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Review 5.  Down syndrome: the brain in trisomic mode.

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7.  Cognitive and sensorimotor tasks for assessing functional impairments in mouse models of Alzheimer's disease and related disorders.

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8.  Rapid forgetting of social learning in the Ts65Dn mouse model of Down syndrome: New evidence for hippocampal dysfunction.

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Journal:  Behav Neurosci       Date:  2018-02       Impact factor: 1.912

9.  Size does not always matter: Ts65Dn Down syndrome mice show cerebellum-dependent motor learning deficits that cannot be rescued by postnatal SAG treatment.

Authors:  Nicolas Gutierrez-Castellanos; Beerend H J Winkelman; Leonardo Tolosa-Rodriguez; Benjamin Devenney; Roger H Reeves; Chris I De Zeeuw
Journal:  J Neurosci       Date:  2013-09-25       Impact factor: 6.167

10.  A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome.

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Journal:  Hum Mol Genet       Date:  2009-09-26       Impact factor: 6.150

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