N-methyl-D-aspartate receptors strongly regulate postsynaptic activity levels during optic nerve regeneration.

Published

Journal Article

During development, neuronal activity is used as a cue to guide synaptic rearrangements to refine connections. Many studies, especially in the visual system, have shown that the N-methyl-D-aspartate receptor (NMDAr) plays a key role in mediating activity-dependent refinement through long-term potentiation (LTP)-like processes. Adult goldfish can regenerate their optic nerve and utilize neuronal activity to generate precise topography in their projection onto tectum. Although the NMDAr has been implicated in this process, its precise role in regeneration has not been extensively studied. In examining NMDAr function during regeneration, we found salient differences compared with development. By using field excitatory postsynaptic potential (fEPSP) recordings, the contribution of the NMDAr at the primary optic synapse was measured. In contrast to development, no increase in NMDAr function was detectable during synaptic refinement. Unlike development, LTP could not be reliably elicited during regeneration. Unexpectedly, we found that NMDAr exerted a major effect on regulating ongoing tectal (postsynaptic) activity levels during regeneration. Blocking NMDAr strongly suppressed spontaneous activity during regeneration but had no significant effect in the normal projection. This difference could be attributed to an occlusion effect of strong optic drive in the normal projection, which dominated ongoing tectal activity. During regeneration, this optic drive is largely absent. Optic nerve stimulation further indicated that the NMDAr had little effect on the ability of optic fibers to evoke early postsynaptic impulse activity but was important for late network activity. These results indicate that, during regeneration, the NMDAr may play a critical role in the homeostatic regulation of ongoing activity and network excitability.

Full Text

Duke Authors

Cited Authors

  • Kolls, BJ; Meyer, RL

Published Date

  • October 2013

Published In

Volume / Issue

  • 91 / 10

Start / End Page

  • 1263 - 1279

PubMed ID

  • 23873725

Pubmed Central ID

  • 23873725

Electronic International Standard Serial Number (EISSN)

  • 1097-4547

Digital Object Identifier (DOI)

  • 10.1002/jnr.23246

Language

  • eng

Conference Location

  • United States