Acetylcholine receptors from human muscle as pharmacological targets for ALS therapy
Pathogenesis
Palmitoylethanolamide
DOI:
10.1073/pnas.1600251113
Publication Date:
2016-03-01T04:14:31Z
AUTHORS (11)
ABSTRACT
Significance Amyotrophic lateral sclerosis (ALS) is a fatal disease leading to motor neuron degeneration and progressive paralysis. Other studies have revealed defects in skeletal muscle even the absence of anomalies, focusing on acetylcholine receptors (AChRs) supporting so-called “dying-back” hypothesis. Our results indicate that endocannabinoid palmitoylethanolamide (PEA) reduces rundown AChRs currents ALS can clinically improve patients’ pulmonary function. This study strengthens important role pathogenesis idea be therapeutic targets.
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