Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disease of adults which preferentially attacks the neuromotor system. Riluzole has been used as the …
KC Murray, A Nakae, MJ Stephens, M Rank… - Nature medicine, 2010 - nature.com
Muscle paralysis after spinal cord injury is partly caused by a loss of brainstem-derived serotonin (5-HT), which normally maintains motoneuron excitability by regulating crucial …
All movements are generated by the activation of motoneurons, and hence their input-output properties define the final step in processing of all motor commands. A major challenge to …
ML Martinez-Silva, RD Imhoff-Manuel, A Sharma… - Elife, 2018 - elifesciences.org
Hyperexcitability has been suggested to contribute to motoneuron degeneration in amyotrophic lateral sclerosis (ALS). If this is so, and given that the physiological type of a …
The excitability of spinal motoneurons is both fundamental for motor behavior and essential in diagnosis of neural disorders. There are two mechanisms for altering this excitability. The …
Persistent inward currents (PICs) are present in many types of neurons and likely have diverse functions. In spinal motoneurons, PICs are especially strong, primarily located in …
It is now accepted that neurons contain and release multiple transmitter substances. However, we still have only limited insight into the regulation and functional effects of this co …
JM D'amico, EG Condliffe, KJB Martins… - Frontiers in integrative …, 2014 - frontiersin.org
The state of areflexia and muscle weakness that immediately follows a spinal cord injury (SCI) is gradually replaced by the recovery of neuronal and network excitability, leading to …
DF Collins - Exercise and sport sciences reviews, 2007 - journals.lww.com
COLLINS, DF Central contributions to contractions evoked by tetanic neuromuscular electrical stimulation. Exerc. Sport Sci. Rev., Vol. 35, No. 3, pp. 102Y109, 2007. Tetanic …