Emergence of Treadmill Running Ability and Quantitative Assessment of Gait Dynamics in Young Ts65Dn Mice: A Mouse Model for Down Syndrome.

Ts65Dn mouse balance down syndrome motor control neurodevelopment trisomy 21

Journal

Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646

Informations de publication

Date de publication:
29 Apr 2023
Historique:
received: 01 04 2023
revised: 18 04 2023
accepted: 28 04 2023
medline: 27 5 2023
pubmed: 27 5 2023
entrez: 27 5 2023
Statut: epublish

Résumé

Down syndrome (DS), which results from the complete or partial trisomy of chromosome 21 (trisomy-21), is the most common genetically defined cause of intellectual disability. Trisomy-21 also produces, or is associated with, many neurodevelopmental phenotypes and neurological comorbidities, including delays and deficits in fine and gross motor development. The Ts65Dn mouse is the most studied animal model for DS and displays the largest known subset of DS-like phenotypes. To date, however, only a small number of developmental phenotypes have been quantitatively defined in these animals. Here, we used a commercially available high-speed, video-based system to record and analyze the gait of Ts65Dn and euploid control mice. Longitudinal treadmill recordings were performed from p17 to p35. One of the main findings was the detection of genotype- and sex-dependent developmental delays in the emergence of consistent, progressive-intensity gait in Ts65Dn mice when compared to control mice. Gait dynamic analysis showed wider normalized front and hind stances in Ts65Dn mice compared to control mice, which may reflect deficits in dynamic postural balance. Ts65Dn mice also displayed statistically significant differences in the variability in several normalized gait measures, which were indicative of deficits in precise motor control in generating gait.

Identifiants

pubmed: 37239215
pii: brainsci13050743
doi: 10.3390/brainsci13050743
pmc: PMC10216633
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Alana's Foundation
ID : 124124

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Auteurs

Jonah J Scott-McKean (JJ)

Department of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

Ryan Jones (R)

College of Medicine and Life Sciences, The University of Toledo, Toledo, OH 43606-3390, USA.
Department of Biochemistry, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

Mark W Johnson (MW)

Department of Pediatrics, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

Joyce Mier (J)

Physical Therapy Program, University of Wisconsin, Madison, WI 53706-1532, USA.
Department of Biology, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

Ines A Basten (IA)

Psychiatric Hospital Asster, 3800 Sint-Truiden, Belgium.

Melissa R Stasko (MR)

Department of Pediatrics, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

Alberto C S Costa (ACS)

Department of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH 44106-6090, USA.
Department of Psychiatry, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

Classifications MeSH