Divergent Modulation of Clinical Measures of Volitional
and Reflexive Motor Behaviors following Serotonergic
Medications in Human Incomplete Spinal Cord Injury
posted on 2015-08-13, 00:00authored byChristopher K. Thompson, T. George Hornby
Incomplete spinal cord injury (SCI) can result in profound impairments in volitional strength and reflex excitability, which
contribute to loss of function. Human and animal models suggest that disruption of endogenous monoaminergic input,
particularly serotonin (5-HT), from supraspinal centers contributes to this impaired motor function following SCI. In the
present study, we investigated the effects of 5-HT medications on motor function in individuals with chronic ( > 1 year)
SCI. Clinical measures of strength, spasticity/spasms, and walking ability were assessed in 12 individuals with chronic
incomplete SCI following acute administration of either 8mg cyproheptadine, a 5-HT antagonist, or 10 mg escitalopram, a
selective 5-HT reuptake inhibitor (SSRI), in a double-blinded, randomized, crossover fashion. Results indicated that 5-HT
medications modulated both volitional and reflexive behaviors with little change in walking performance; 5-HT antagonist
medications depressed clinical measures of strength and spasticity/spasms, whereas SSRIs augmented both strength and
spasticity/spasms. These changes are consistent with the dysregulation of 5-HT sensitive spinal neurons following SCI.
This understanding may augment clinicians’ awareness of the motor consequences of 5-HT medications.
Funding
Funding for the present work was provided through a University
of Illinois at Chicago (UIC) doctoral scholarship and Foundation
for Physical Therapy Scholarship to Dr. Thompson and National
Institutes of Health (NIH)/National Institute of Child Health and
Human Development (NICHD) R21-HD046876 and the Craig H.
Neilsen Foundation (grant # 36830) to Dr. Hornby.