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Early Detection of Motor Dysfunction in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Using Home Cage Running Wheels
by
Shaw, Pamela J.
, Azzouz, Mimoun
, Mead, Richard J.
, Grierson, Andrew J.
, Bennett, Ellen J.
in
Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - diagnosis
/ Amyotrophic Lateral Sclerosis - genetics
/ Amyotrophic Lateral Sclerosis - mortality
/ Amyotrophic Lateral Sclerosis - physiopathology
/ Animal Welfare - ethics
/ Animals
/ Biology and Life Sciences
/ Cages
/ Disease Models, Animal
/ Disease Progression
/ Early Diagnosis
/ Female
/ Male
/ Medicine and Health Sciences
/ Mice
/ Mice, Transgenic
/ Motor Neurons - metabolism
/ Motor Neurons - pathology
/ Mutation
/ Research and Analysis Methods
/ Rodents
/ Rotarod Performance Test - instrumentation
/ Rotarod Performance Test - methods
/ Running
/ Studies
/ Superoxide dismutase
/ Superoxide Dismutase - genetics
/ Superoxide Dismutase-1
/ Survival Analysis
/ Transgenic mice
/ Wheels
2014
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Early Detection of Motor Dysfunction in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Using Home Cage Running Wheels
by
Shaw, Pamela J.
, Azzouz, Mimoun
, Mead, Richard J.
, Grierson, Andrew J.
, Bennett, Ellen J.
in
Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - diagnosis
/ Amyotrophic Lateral Sclerosis - genetics
/ Amyotrophic Lateral Sclerosis - mortality
/ Amyotrophic Lateral Sclerosis - physiopathology
/ Animal Welfare - ethics
/ Animals
/ Biology and Life Sciences
/ Cages
/ Disease Models, Animal
/ Disease Progression
/ Early Diagnosis
/ Female
/ Male
/ Medicine and Health Sciences
/ Mice
/ Mice, Transgenic
/ Motor Neurons - metabolism
/ Motor Neurons - pathology
/ Mutation
/ Research and Analysis Methods
/ Rodents
/ Rotarod Performance Test - instrumentation
/ Rotarod Performance Test - methods
/ Running
/ Studies
/ Superoxide dismutase
/ Superoxide Dismutase - genetics
/ Superoxide Dismutase-1
/ Survival Analysis
/ Transgenic mice
/ Wheels
2014
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Early Detection of Motor Dysfunction in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Using Home Cage Running Wheels
by
Shaw, Pamela J.
, Azzouz, Mimoun
, Mead, Richard J.
, Grierson, Andrew J.
, Bennett, Ellen J.
in
Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - diagnosis
/ Amyotrophic Lateral Sclerosis - genetics
/ Amyotrophic Lateral Sclerosis - mortality
/ Amyotrophic Lateral Sclerosis - physiopathology
/ Animal Welfare - ethics
/ Animals
/ Biology and Life Sciences
/ Cages
/ Disease Models, Animal
/ Disease Progression
/ Early Diagnosis
/ Female
/ Male
/ Medicine and Health Sciences
/ Mice
/ Mice, Transgenic
/ Motor Neurons - metabolism
/ Motor Neurons - pathology
/ Mutation
/ Research and Analysis Methods
/ Rodents
/ Rotarod Performance Test - instrumentation
/ Rotarod Performance Test - methods
/ Running
/ Studies
/ Superoxide dismutase
/ Superoxide Dismutase - genetics
/ Superoxide Dismutase-1
/ Survival Analysis
/ Transgenic mice
/ Wheels
2014
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Early Detection of Motor Dysfunction in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Using Home Cage Running Wheels
Journal Article
Early Detection of Motor Dysfunction in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Using Home Cage Running Wheels
2014
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Overview
The SOD1G93A mouse has been used since 1994 for preclinical testing in amyotrophic lateral sclerosis (ALS). Despite recent genetic advances in our understanding of ALS, transgenic mice expressing mutant SOD1 remain the best available, and most widely used, vertebrate model of the disease. We previously described an optimised and rapid approach for preclinical studies in the SOD1G93A mouse. Here we describe improvements to this approach using home cage running wheels to obtain daily measurements of motor function, with minimal intervention. We show that home cage running wheels detect reductions in motor function at a similar time to the rotarod test, and that the data obtained are less variable allowing the use of smaller groups of animals to obtain satisfactory results. This approach refines use of the SOD1G93A model, and reduces the number of animals undergoing procedures of substantial severity, two central principles of the 3Rs (replacement, reduction and refinement of animal use in research). The small group sizes and rapid timescales enable affordable large-scale therapeutic pre-screening in the SOD1G93A mouse, as well as rapid validation of published positive effects in a second laboratory, one of the major stumbling blocks in ALS preclinical therapy development.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Amyotrophic Lateral Sclerosis - diagnosis
/ Amyotrophic Lateral Sclerosis - genetics
/ Amyotrophic Lateral Sclerosis - mortality
/ Amyotrophic Lateral Sclerosis - physiopathology
/ Animals
/ Cages
/ Female
/ Male
/ Medicine and Health Sciences
/ Mice
/ Mutation
/ Research and Analysis Methods
/ Rodents
/ Rotarod Performance Test - instrumentation
/ Rotarod Performance Test - methods
/ Running
/ Studies
/ Superoxide Dismutase - genetics
/ Wheels
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