¹Department of Anatomy and Physiology, Research Centre of the Laval University Medical center, Laval University, Quebec, Canada

Correspondence: PA Guertin, Research Centre of the Laval University Medical Center, 2705 Bld Laurier, RC-9800, Quebec City, (Quebec), Canada G1v4G2

Abstract

Study design: Experimental laboratory investigation of the effects of serotonergic and glutamatergic drugs in early paraplegic mice.

Objectives: To examine whether NMDA and 5-HT receptors synergistically participate to generate basic stepping movements in paraplegic mice.

Setting: Laval University Medical Center, Quebec, Canada.

Methods: Adult mice completely spinalized at the low-thoracic level 1 week earlier were suspended in harnesses for experiments. Acute drug-induced effects were examined on hindlimb movements filmed with a digital video camera. Detailed kinematic analyses included stick diagrams reconstructions of hindlimb movements and analysis of bilateral coordination, angular excursion, stepping amplitude and frequency.

Results: A single treatment with the 5-HT₂ agonist quipazine (>0.7 mg/kg, i.p.) induced episodes of air-stepping movements in the hindlimbs of paraplegic mice. In contrast, injection of the glutamatergic agonist NMDA (1–45 mg/kg i.p.) failed to induce rhythmicity, although nonlocomotor rhythmic movements were observed with higher doses (45–60 mg/kg i.p.). Subthreshold doses of NMDA (22–30 mg/kg) could induce episodes of hindlimb air-stepping if combined with subthreshold doses of quipazine (0.3–0.7 mg/kg). Air-stepping was entirely blocked by administration of the selective NMDA antagonist MK-801.

Conclusion: A single treatment with quipazine can trigger episodes of locomotor-like movements in early chronic spinal mice. Even though NMDA alone could not generate bilaterally coordinated air-stepping, NMDA receptor activation was nonetheless critical for spinal locomotor rhythmogenesis induced by 5-HT agonists in awake behaving animals.