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Cited by 1,102

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity

Liu, Lidong, Wong, Tak Pan, Pozza, Mario F., Lingenhoehl, Kurt, Wang, Yushan, Sheng, Morgan, Auberson, Yves P., Wang, Yu Tian·2004·Science

Abstract

Activation of N -methyl- d -aspartate subtype glutamate receptors (NMDARs) is required for long-term potentiation (LTP) and long-term depression (LTD) of excitatory synaptic transmission at hippocampal CA1 synapses, the proposed cellular substrates of learning and memory. However, little is known about how activation of NMDARs leads to these two opposing forms of synaptic plasticity. Using hippocampal slice preparations, we showed that selectively blocking NMDARs that contain the NR2B subunit abolishes the induction of LTD but not LTP. In contrast, preferential inhibition of NR2A-containing NMDARs prevents the induction of LTP without affecting LTD production. These results demonstrate that distinct NMDAR subunits are critical factors that determine the polarity of synaptic plasticity.

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Metadata

Authors
Liu, L., Wong, T. P., Pozza, M. F., Lingenhoehl, K., Wang, Y., Sheng, M., Auberson, Y. P., & Wang, Y. T.
Venue
Science
Published
2004-05-14
Volume
304
Issue
5673
Pages
1021-1024
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2028594041
Cited by
1,102
References
6
FWCI
29.51
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity. https://app.cochat.ai/papers/10.1126/science.1096615
The paper
Liu, L., Wong, T. P., Pozza, M. F., Lingenhoehl, K., Wang, Y., Sheng, M., Auberson, Y. P., & Wang, Y. T. (2004). Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity. Science. https://doi.org/10.1126/science.1096615

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.