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Increasing motor neuron excitability to treat weakness in sepsis
Author(s) -
Nardelli Paul,
Powers Randall,
Cope Tim C.,
Rich Mark M.
Publication year - 2017
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.25105
Subject(s) - weakness , neuroscience , motor neuron , agonist , medicine , intensive care unit , muscle weakness , motor unit , psychology , intensive care medicine , receptor , spinal cord , surgery
Objective Weakness induced by critical illness (intensive care unit acquired weakness) is a major cause of disability in patients and is currently untreatable. We recently identified a defect in repetitive firing of lower motor neurons as a novel contributor to intensive care unit acquired weakness. To develop therapy for intensive care unit acquired weakness, it was necessary to determine the mechanism underlying the defect in repetitive firing. Methods Both computer simulation and in vivo dynamic voltage clamp of spinal motor neurons in septic rats were employed to explore potential mechanisms underlying defective repetitive firing. Results Our results suggest alteration in subthreshold voltage‐activated currents might be the mechanism underlying defective repetitive firing. It has been shown previously that pharmacologic activation of serotonin receptors on motor neurons increases motor neuron excitability, in part by enhancing subthreshold voltage‐activated inward currents. Administration of a U.S. Food and Drug Administration–approved serotonin agonist (lorcaserin) to septic rats greatly improved repetitive firing and motor unit force generation. Interpretation Our findings suggest activation of serotonin receptors with lorcaserin may provide the first ever therapy for intensive care unit acquired weakness in patients. Ann Neurol 2017;82:961–971