Alpha-1 adrenoceptor agonists generate a fast NMDA receptor-independent motor rhythm in the neonatal rat spinal cord

Noradrenaline, a potent activator of rhythmogenic networks in adult mammals has not been reported to produce functional rhythmic patterns in isolated spinal cords of newborn rats. We now show that a fast (cycle time: 1-4 s) transient rhythm was induced in sacrococcygeal (SC) and rostral-lumbar spinal segments of the neonatal rat by bath-applied noradrenaline. The fast rhythm was blocked by 1 muM of the alpha1-adrenoceptor antagonist prazosin but not by 1-20 muM of the alpha2-adrenoceptor blocker yohimbine, it could be initiated and maintained by alpha1-adrenoceptor agonists, and it was accompanied by a slow nonlocomotor rhythm. Transection at the lumbosacral junction abolished the fast-thoracolumbar (TL) rhythm while the fast-SC and slow-TL rhythms were unaffected. The N-methyl-D-aspartate (NMDA) receptor antagonist 2-amino-5-phosphonopentanoic acid (AP5) abolished the slow- and did not interrupt the fast rhythm. Thus alpha1-adrenoceptor agonists induce an NMDA receptor-independent rhythm in the SC cord and modulate NMDA receptor-dependent rhythmicity in TL segments. Injection of current steps into S-2 and flexor-dominated L-2 motoneurons during the fast rhythm revealed a 20-30% decrease in input-resistance (R-N), coinciding with contralateral bursting. The R-N of extensor-dominated L-5 motoneurons did not vary with the fast rhythm. The rhythmic fluctuations of R-N in L-2 motoneurons were abolished, but the alternating left-right pattern of the fast rhythm was unchanged in midsagittally split TL cords. We suggest that the locomotor generators were not activated during the fast rhythm, that crossed-inhibitory pathways activated by SC projections controlled the rhythmic decrease in R-N in L-2 motoneurons, and that the alternating pattern of the split TL cord was maintained by excitatory SC projections.