Literature DB >> 27575947

Neurobehavioral deficits in the KIKO mouse model of Friedreich's ataxia.

Marissa Z McMackin1, Chelsea K Henderson1, Gino A Cortopassi2.   

Abstract

Friedreich's Ataxia (FA) is a pediatric neurodegenerative disease whose clinical presentation includes ataxia, muscle weakness, and peripheral sensory neuropathy. The KIKO mouse is an animal model of FA with frataxin deficiency first described in 2002, but neurobehavioral deficits have never been described in this model. The identification of robust neurobehavioral deficits in KIKO mice could support the testing of drugs for FA, which currently has no approved therapy. We tested 13 neurobehavioral tasks to identify a robust KIKO phenotype: Open Field, Grip Strength Test(s), Cylinder, Skilled Forelimb Grasp Task(s), Treadmill Endurance, Locotronic Motor Coordination, Inverted Screen, Treadscan, and Von Frey. Of these, Inverted Screen, Treadscan and Von Frey produced significant neurobehavioral deficits at >8 months of age, and relate to the clinically relevant endpoints of muscle strength and endurance, gait ataxia, and peripheral insensitivity. Thus we identify robust phenotypic measures related to Friedreich's ataxia clinical endpoints which could be used to test effectiveness of potential drug therapy.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Ataxia; Automated gait analysis; Frataxin; Friedreich’s ataxia; Inverted screen; Neurobehavioral; Peripheral sensitivity; Von Frey

Mesh:

Substances:

Year:  2016        PMID: 27575947      PMCID: PMC5051948          DOI: 10.1016/j.bbr.2016.08.053

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  37 in total

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3.  Nrf2 Induction Re-establishes a Proper Neuronal Differentiation Program in Friedreich's Ataxia Neural Stem Cells.

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7.  Potential biomarker identification for Friedreich's ataxia using overlapping gene expression patterns in patient cells and mouse dorsal root ganglion.

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  7 in total

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