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Selective enhancement of non-NMDA receptor-mediated responses following induction of long-term potentiation in entorhinal cortex

Authors :
Yun, Sung Hwan
Huh, Kyoon
Jung, Min Whan
Source :
Synapse; January 2000, Vol. 35 Issue: 1 p1-7, 7p
Publication Year :
2000

Abstract

The contribution of NMDA receptors to the expression of long-term potentiation (LTP) is controversial. In entorhinal cortex (EC) previous studies reported either that LTP was exclusively expressed through NMDA receptors or that both NMDA and non-NMDA receptors were involved in LTP expression. To reexamine this issue, horizontal entorhinal cortical slices were prepared from adult rats and electrical stimulation was delivered in layer II/III, while field potential recordings were made in layer III. In the standard condition (2.5 mM Mg<SUP>++</SUP>), LTP was reliably induced by theta burst stimulation, but was blocked by 100 μM D-AP5, an NMDA receptor antagonist. This corroborates previous reports that NMDA receptor activation is required for induction of EC LTP. The field potential response was not affected by D-AP5, but completely blocked by 10 μM CNQX, a non-NMDA receptor antagonist. This indicates that the expression of LTP is mediated by non-NMDA receptors in the standard condition. LTP of NMDA receptor-mediated responses was tested by comparing NMDA responses before and after applying theta burst stimulation in medium containing low magnesium (0.4–1 mM). Theta burst stimulation induced 43.2±9.7% increase of non-NMDA responses (i.e., AP5-insensitive fast component) but 5.6±9.0% decrease of the NMDA receptor component (AP5-sensitive slow component). These results indicate that activation of NMDA receptors is critical for induction of LTP, but LTP expression is mediated by non-NMDA receptors in EC under these experimental conditions. Synapse 34:1–7, 2000. © 2000 Wiley-Liss, Inc.

Details

Language :
English
ISSN :
08874476 and 10982396
Volume :
35
Issue :
1
Database :
Supplemental Index
Journal :
Synapse
Publication Type :
Periodical
Accession number :
ejs2345885
Full Text :
https://doi.org/10.1002/(SICI)1098-2396(200001)35:1<1::AID-SYN1>3.0.CO;2-L