Skip to main content

Research Repository

Advanced Search

Medium-Chain Fatty Acids Rescue Motor Function and Neuromuscular Junction Degeneration in a Drosophila Model of Amyotrophic Lateral Sclerosis

Dunn, Ella; Steinert, Joern R.; Stone, Aelfwin; Sahota, Virender; Williams, Robin S. B.; Snowden, Stuart; Augustin, Hrvoje

Medium-Chain Fatty Acids Rescue Motor Function and Neuromuscular Junction Degeneration in a Drosophila Model of Amyotrophic Lateral Sclerosis Thumbnail


Authors

Ella Dunn

Aelfwin Stone

Virender Sahota

Robin S. B. Williams

Stuart Snowden

Hrvoje Augustin



Contributors

Maurizio Romano
Editor

Abstract

Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease characterised by progressive degeneration of the motor neurones. An expanded GGGGCC (G4C2) hexanucleotide repeat in C9orf72 is the most common genetic cause of ALS and frontotemporal dementia (FTD); therefore, the resulting disease is known as C9ALS/FTD. Here, we employ a Drosophila melanogaster model of C9ALS/FTD (C9 model) to investigate a role for specific medium-chain fatty acids (MCFAs) in reversing pathogenic outcomes. Drosophila larvae overexpressing the ALS-associated dipeptide repeats (DPRs) in the nervous system exhibit reduced motor function and neuromuscular junction (NMJ) defects. We show that two MCFAs, nonanoic acid (NA) and 4-methyloctanoic acid (4-MOA), can ameliorate impaired motor function in C9 larvae and improve NMJ degeneration, although their mechanisms of action are not identical. NA modified postsynaptic glutamate receptor density, whereas 4-MOA restored defects in the presynaptic vesicular release. We also demonstrate the effects of NA and 4-MOA on metabolism in C9 larvae and implicate various metabolic pathways as dysregulated in our ALS model. Our findings pave the way to identifying novel therapeutic targets and potential treatments for ALS.

Citation

Dunn, E., Steinert, J. R., Stone, A., Sahota, V., Williams, R. S. B., Snowden, S., & Augustin, H. (2023). Medium-Chain Fatty Acids Rescue Motor Function and Neuromuscular Junction Degeneration in a Drosophila Model of Amyotrophic Lateral Sclerosis. Cells, 12(17), Article 2163. https://doi.org/10.3390/cells12172163

Journal Article Type Article
Acceptance Date Aug 22, 2023
Online Publication Date Aug 28, 2023
Publication Date 2023-09
Deposit Date Sep 1, 2023
Publicly Available Date Sep 4, 2023
Journal Cells
Electronic ISSN 2073-4409
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 12
Issue 17
Article Number 2163
DOI https://doi.org/10.3390/cells12172163
Keywords ALS; MCFA; 4-MOA; NA; Drosophila; motor function; NMJ; glutamate
Public URL https://nottingham-repository.worktribe.com/output/24870171
Publisher URL https://www.mdpi.com/2073-4409/12/17/2163

Files





You might also like



Downloadable Citations