Affiliation:
1. Department of Physiology and Medical Physics, Centre for the Study of Neurological Disorders, Royal College of Surgeons in Ireland, 123 St. Stephen’s Green, Dublin 2, Ireland
Abstract
Transgenic transactivation response DNA-binding protein 43 (TDP-43) mice expressing the A315T mutation under the control of the murine prion promoter progressively develop motor function deficits and are considered a new model for the study of ALS; however, pre-mature sudden death due to intestinal obstruction halts disease phenotype progression in 100% C57Bl6/J congenic TDP-43A315T mice. We recently identified elevated adenosine-mono-phosphate kinase (AMPK) activation in SOD1G93A mice, indicating increased energetic stress during disease progression. Similar to SOD1G93A mice, TDP-43A315T mice fed a standard pellet diet showed increased AMPK activation at postnatal day (PND) 80. We therefore investigated the effects of a high fat jelly diet on bioenergetic status and life span in TDP-43A315T mice. No difference in AMPK activation was detected in high fat jelly-fed TDP-43A315T mice up to PND 120. Direct comparison of high fat jelly diet and standard pellet diet mice also showed decreased phosphorylation of acetyl-CoA carboxylase (ACC) at early stage time points on high fat jelly diet. Exposure to high fat jelly diet prevented sudden death and extended survival (147±27 days compared to 102±19 days on standard pellet diet; p=<0.001). High fat jelly-fed mice developed a motor neuron disease phenotype with significantly decreased body weight from PND 80 onward that was characterised by deficits in Rotarod abilities (PND 130, 130, 150) and stride length measurements (PND 100 onward). Development of this phenotype was associated with a significant motor neuron loss as assessed by Nissl staining of motor neurons in the lumbar spinal cord. Our work suggests that a high fat jelly diet vastly improves the pre-clinical utility of the TDP-43A315T model by extending lifespan and allowing the motor neuron disease phenotype to progress. Our data additionally indicate the potential benefit of a high fat jelly diet in TDP-43-associated ALS.
Funder
Science Foundation Ireland with Pfizer
Centres of Excellence in Neurodegeneration
Publisher
The Company of Biologists
Subject
General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)
Cited by
47 articles.
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