HIGH-AFFINITY AND LOW-AFFINITY NMDA RECEPTOR-BINDING SITES IN RAT SPINAL-CORD - EFFECTS OF TRAUMATIC INJURY

N-methyl-D-aspartate (NMDA) receptor-mediated events hade been implicated in the pathophysiology of posttraumatic spinal. cord injury. In the present study, [H-3]MK801 was used to analyse the changes in NMDA receptor-binding sites in rat spinal cord after impact trauma at T9. In contrast to brain, which showed only a single binding site, spinal cord showed both high-affinity (K-d1 = 0.47 +/- 0.24 nM) and low-affinity (K-d2 = 7.75 +/- 1.82 nM) binding sites with relatively low binding density (B-max1 = 0.11 +/- 0.04 pmol/mg protein and B-max2 = 0.84 +/- 0.11 pmol/mg protein). Time-course studies demonstrated significant decreases in the binding of [H-3]MK801 at the thoracic and lumbar segments at 4 h after spinal cord injury with recovery by 24 h. Scatchard analyses indicate that these changes likely involve bath high- and low-affinity binding sites. The transitory reduction in [H-3]MK801-binding after trauma may reflect downregulation of NMDA receptors as a consequence of posttraumatic glutamate release and may serve to limit excitotoxin-induced injury.