Correlation Engine 2.0
Clear Search sequence regions


Sizes of these terms reflect their relevance to your search.

Duchenne muscular dystrophy (DMD), myotonic dystrophy type 1 (DM1), and spinal muscular atrophy (SMA) are the most prevalent neuromuscular disorders (NMDs) in children and adults. Central to a healthy neuromuscular system are the processes that govern mitochondrial turnover and dynamics, which are regulated by AMP-activated protein kinase (AMPK). Here, we survey mitochondrial stresses that are common between, as well as unique to, DMD, DM1, and SMA, and which may serve as potential therapeutic targets to mitigate neuromuscular disease. We also highlight recent advances that leverage a mutation-agnostic strategy featuring physiological or pharmacological AMPK activation to enhance mitochondrial health in these conditions, as well as identify outstanding questions and opportunities for future pursuit. Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Citation

Andrew I Mikhail, Sean Y Ng, Stephanie R Mattina, Vladimir Ljubicic. AMPK is mitochondrial medicine for neuromuscular disorders. Trends in molecular medicine. 2023 Jul;29(7):512-529

Expand section icon Mesh Tags

Expand section icon Substances


PMID: 37080889

View Full Text