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Optimizing the Translational Value of Mouse Models of ALS for Dysphagia Therapeutic Discovery

Authors :
Sabrina Kohlberg
Alexis Mok
Andries Ferreira
Joan R. Coates
Kate L Osman
Katelyn McCormack
Elizabeth A. Bearce
Matan D. Kadosh
Mary K. Fagan
Teresa E. Lever
Nicole L. Nichols
Lori A Lind
Ryan T. Brooks
Source :
Dysphagia
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

The goal of this study was to compare dysphagia phenotypes in low and high copy number (LCN and HCN) transgenic superoxide dismutase 1 (SOD1) mouse models of ALS to accelerate the discovery of novel and effective treatments for dysphagia and early amyotrophic lateral sclerosis (ALS) diagnosis. Clinicopathological features of dysphagia were characterized in individual transgenic mice and age-matched controls utilizing videofluoroscopy in conjunction with postmortem assays of the tongue and hypoglossal nucleus. Quantitative PCR accurately differentiated HCN-SOD1 and LCN-SOD1 mice and nontransgenic controls. All HCN-SOD1 mice developed stereotypical paralysis in both hindlimbs. In contrast, LCN-SOD1 mice displayed wide variability in fore- and hindlimb involvement. Lick rate, swallow rate, inter-swallow interval, and pharyngeal transit time were significantly altered in both HCN-SOD1 and LCN-SOD1 mice compared to controls. Tongue weight, tongue dorsum surface area, total tongue length, and caudal tongue length were significantly reduced only in the LCN-SOD1 mice compared to age-matched controls. LCN-SOD1 mice with lower body weights had smaller/lighter weight tongues, and those with forelimb paralysis and slower lick rates died at a younger age. LCN-SOD1 mice had a 32% loss of hypoglossal neurons, which differed significantly when compared to age-matched control mice. These novel findings for LCN-SOD1 mice are congruent with reported dysphagia and associated tongue atrophy and hypoglossal nucleus pathology in human ALS patients, thus highlighting the translational potential of this mouse model in ALS research.

Details

ISSN :
14320460 and 0179051X
Volume :
35
Database :
OpenAIRE
Journal :
Dysphagia
Accession number :
edsair.doi.dedup.....39107e97a8f1b727c9579dc86e9d9fc0