Recovery of locomotor function with combinatory drug treatments designed to synergistically activate specific neuronal networks

Curr Med Chem. 2009;16(11):1366-71. doi: 10.2174/092986709787846541.

Abstract

Spinal cord injury (SCI) is a devastating condition generally leading to a permanent and irreversible loss of sensory and motor functions. We have identified recently a number of serotonergic, adrenergic and dopaminergic receptor agonists or precursors that can acutely elicit some motor and locomotor-like movements in completely spinal cord-transected (thoracic level) animals. However, only partial central network-activating effects were found with single molecules since none administered separately could elicit weight-bearing and functional stepping movements in Tx animals. In turn, a recent breakthrough revealed that full spinal locomotor network-activating effects may be induced with synergistic drug combinations. Indeed, specific cocktails comprising some of these agonists and precursors were found, indeed, to powerfully generate weight-bearing stepping with plantar foot placement in untrained, non-assisted and non-sensory-stimulated Tx mice. This significant finding provides clear evidence suggesting that combinatorial approaches based on drug-drug synergistic interactions may constitute innovative solutions for the design and development of novel pharmacological therapies in the field of SCI and related neurological disorders.

MeSH terms

  • Animals
  • Dopamine / metabolism
  • Dopamine Agonists / pharmacology
  • Dopamine Agonists / therapeutic use*
  • Drug Synergism
  • Humans
  • Levodopa / pharmacology
  • Locomotion / drug effects*
  • Rehabilitation
  • Serotonin / metabolism
  • Serotonin Receptor Agonists / pharmacology
  • Serotonin Receptor Agonists / therapeutic use*
  • Spinal Cord Injuries / drug therapy*
  • Spinal Cord Injuries / physiopathology
  • Spinal Cord Injuries / therapy

Substances

  • Dopamine Agonists
  • Serotonin Receptor Agonists
  • Serotonin
  • Levodopa
  • Dopamine