Dorsal hippocampus NMDA receptors differentially mediate trace and contextual fear conditioning

The dorsal hippocampus (DH) is critically involved in the acquisition and expression of trace and contextual fear conditioning. NMDA/glutamate receptor‐mediated transmission is thought to be one mechanism mediating the plastic changes that support long‐term memories in the DH. However, their precise...

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Bibliographic Details
Published in:Hippocampus Vol. 15; no. 5; pp. 665 - 674
Main Authors: Quinn, Jennifer J., Loya, Fred, Ma, Quang D., Fanselow, Michael S.
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 2005
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Summary:The dorsal hippocampus (DH) is critically involved in the acquisition and expression of trace and contextual fear conditioning. NMDA/glutamate receptor‐mediated transmission is thought to be one mechanism mediating the plastic changes that support long‐term memories in the DH. However, their precise involvement in acquisition and expression processes has not been defined. To examine this issue, the NMDA receptor antagonist, D,L‐2‐amino‐5‐phosphonovaleric acid (APV; 10 μg/μl; 0.5 μl), was infused into the DH prior to conditioning and/or testing, using a trace fear conditioning procedure. All rats were tested for freezing to both tone and context in separate, counterbalanced sessions. The three sessions (1 training and 2 test) were separated by approximately 24 h. Using this design, it was possible to assess the role for DH NMDA receptors in the acquisition versus expression of trace and contextual fear conditioning. APV disrupted acquisition, but not expression, of contextual fear conditioning. By contrast, APV attenuated both acquisition and expression of trace fear memories. Thus, DH NMDA receptors appear to contribute to retrieval of some, but not all, fear memories. ©2005 Wiley‐Liss, Inc.
Bibliography:NIMH - No. 1F31MH66549
ark:/67375/WNG-LNW20WGM-1
istex:B7B820CCA9C231D08DB4790880F5479DCA408A2E
ArticleID:HIPO20088
NSF - No. IBN9723295
NIMH - No. MH62122
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1050-9631
1098-1063
DOI:10.1002/hipo.20088