Dual-component NMDA receptor currents at a single central synapse

E. D'Angelo, P. Rossi, J. Garthwaite

Research output: Contribution to journalArticlepeer-review


PRESENT thinking about the way that the NMDA (N-methyl-D-aspartate) class of glutamate receptor operates at central synapses relies mainly on information obtained from single-channel and whole-cell recordings from cultured neurons stimulated by exogenous NMDA receptor agonists1,2. The mechanisms that operate in the postsynaptic membrane of a normal neuron following release of the natural transmitter are far less clear. An important problem is that most normal neurons receive many excitatory synapses (103-105 per cell) and these synapses are located on slender dendritic elements far away from the somatic recording site, making the study of discrete synaptic events difficult. Typically, when populations of synapses are activated, NMDA receptor-mediated synaptic potentials appear as slowly rising, long-lasting waves superimposed on faster, non-NMDA-receptor potentials2-8. Although believed to be critical for NMDA receptor function9,10, this slow time-course would not be predicted from single-channel kinetics and its origin remains puzzling. We have now analysed the events occurring at the level of a single excitatory synapse using a simple, small, neuron - the cerebellar granule cell - which has an unusually simple glutamatergic8 input. By applying high-resolution whole-cell recording techniques to these cells in situ11, we were able to study the nature of elementary NMDA receptor-mediated synaptic currents. Contrary to expectations, the prominent currents are fast but are followed by slow ones. Both types of current are strongly voltage-dependent but differ subtly in this respect. Furthermore, the currents are absent unless glycine is provided.

Original languageEnglish
Pages (from-to)467-470
Number of pages4
Issue number6283
Publication statusPublished - Aug 2 1990

ASJC Scopus subject areas

  • General


Dive into the research topics of 'Dual-component NMDA receptor currents at a single central synapse'. Together they form a unique fingerprint.

Cite this