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The Journal of Neurophysiology Vol. 83 No. 2 February 2000, pp. 955-962
Copyright ©2000 by the American Physiological Society
Neural Plasticity Research Group, Department of Anesthesia and Critical Care, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129
Baba, Hiroshi,
Timothy P. Doubell,
Kimberly A. Moore, and
Clifford J. Woolf.
Silent NMDA Receptor-Mediated Synapses Are Developmentally
Regulated in the Dorsal Horn of the Rat Spinal Cord. J. Neurophysiol. 83: 955-962, 2000. In vitro whole cell
patch-clamp recording techniques were utilized to study silent
pure-N-methyl-D-aspartate (NMDA)
receptor-mediated synaptic responses in lamina II (substantia
gelatinosa, SG) and lamina III of the spinal dorsal horn. To clarify
whether these synapses are present in the adult and contribute to
neuropathic pain, transverse lumbar spinal cord slices were prepared
from neonatal, naive adult and adult sciatic nerve transected rats. In
neonatal rats, pure-NMDA receptor-mediated excitatory postsynaptic currents (EPSCs) were elicited in SG neurons either by focal
intraspinal stimulation (n = 15 of 20 neurons) or
focal stimulation of the dorsal root (n = 2 of 7 neurons). In contrast, in slices from naive adult rats, no silent
pure-NMDA EPSCs were recorded in SG neurons following focal intraspinal
stimulation (n = 27), and only one pure-NMDA EPSC
was observed in lamina III (n = 23). Furthermore, in rats with chronic sciatic nerve transection, pure-NMDA EPSCs were
elicited by focal intraspinal stimulation in only 2 of 45 SG neurons.
Although a large increase in A
fiber evoked mixed
-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and NMDA
receptor-mediated synapses was detected after sciatic nerve injury,
A
fiber-mediated pure-NMDA EPSCs were not evoked in SG neurons by
dorsal root stimulation. Pure-NMDA receptor-mediated EPSCs are
therefore a transient, developmentally regulated phenomenon, and,
although they may have a role in synaptic refinement in the immature
dorsal horn, they are unlikely to be involved in receptive field
plasticity in the adult.
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