 |
The Journal of Neuroscience, May 10, 2006, 26(19):5049-5058; doi:10.1523/JNEUROSCI.4381-05.2006
Previous Article | Next Article 
Behavioral/Systems/Cognitive
Systems Consolidation Requires Postlearning Activation of NMDA Receptors in the Medial Prefrontal Cortex in Trace Eyeblink Conditioning
Kaori Takehara-Nishiuchi,1
Kazuhito Nakao,2
Shigenori Kawahara,1
Norio Matsuki,2 and
Yutaka Kirino1
1Laboratory of Neurobiophysics and 2Laboratory of Chemical Pharmacology, School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 1130033, Japan
Correspondence should be addressed to Kaori Takehara-Nishiuchi, Laboratory of Neurobiophysics, School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan. Email: ktakehara{at}mayqueen.f.u-tokyo.ac.jp
The importance of the hippocampus in declarative memory is limited to recently acquired memory, and remotely acquired memory is believed to be stored somewhere in the neocortex. However, it remains unknown how the memory network is reorganized from a hippocampus-dependent form into a neocortex-dependent one. We reported previously that the medial prefrontal cortex (mPFC) is important for this neocortex-dependent remote memory in rat trace eyeblink conditioning. Here, we investigate the involvement of NMDA receptors in the mPFC in this reorganization and determine the time window of their contribution using chronic infusion of an antagonist into the mPFC, specifically during the postlearning consolidation period. The rats with blockade of the mPFC NMDA receptors during the first 1 or 2 weeks after learning showed a marked impairment in memory retention measured 6 weeks after learning, but relearned normally with subsequent conditioning. In contrast, the same treatment had no effect if it was performed during the third to fourth weeks or during the first day just after learning. The specificity of NMDA receptor blockade was confirmed by the reduced long-term potentiation in the hippocampal-prefrontal pathway in these rats. These results suggest that successful establishment of remotely acquired memory requires activation of NMDA receptors in the mPFC during at least the initial week of the postlearning period. Such NMDA receptor-dependent processes may mediate the maturation of neocortical networks that underlies permanent memory storage and serve as a way to reorganize memory circuitry to the neocortex-dependent form.
Key words: classical conditioning; eyeblink; retention; amnesia; hippocampus; rat; APV; prelimbic; retrieval
Received Oct. 15, 2005;
revised March 24, 2006;
accepted March 24, 2006.
Correspondence should be addressed to Kaori Takehara-Nishiuchi, Laboratory of Neurobiophysics, School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan. Email: ktakehara{at}mayqueen.f.u-tokyo.ac.jp
This article has been cited by other articles:

|
 |

|
 |
 
L. Restivo, G. Vetere, B. Bontempi, and M. Ammassari-Teule
The Formation of Recent and Remote Memory Is Associated with Time-Dependent Formation of Dendritic Spines in the Hippocampus and Anterior Cingulate Cortex
J. Neurosci.,
June 24, 2009;
29(25):
8206 - 8214.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Kolomiets, A. Marzo, J. Caboche, P. Vanhoutte, and S. Otani
Background Dopamine Concentration Dependently Facilitates Long-term Potentiation in Rat Prefrontal Cortex through Postsynaptic Activation of Extracellular Signal-Regulated Kinases
Cereb Cortex,
March 12, 2009;
(2009)
bhp047v1.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. Takehara-Nishiuchi and B. L. McNaughton
Spontaneous Changes of Neocortical Code for Associative Memory During Consolidation
Science,
November 7, 2008;
322(5903):
960 - 963.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Paz, E. P. Bauer, and D. Pare
Theta synchronizes the activity of medial prefrontal neurons during learning
Learn. Mem.,
July 8, 2008;
15(7):
524 - 531.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. J. Quinn, Q. D. Ma, M. R. Tinsley, C. Koch, and M. S. Fanselow
Inverse temporal contributions of the dorsal hippocampus and medial prefrontal cortex to the expression of long-term fear memories
Learn. Mem.,
April 25, 2008;
15(5):
368 - 372.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Gais, G. Albouy, M. Boly, T. T. Dang-Vu, A. Darsaud, M. Desseilles, G. Rauchs, M. Schabus, V. Sterpenich, G. Vandewalle, et al.
Sleep transforms the cerebral trace of declarative memories
PNAS,
November 20, 2007;
104(47):
18778 - 18783.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. R. Euston, M. Tatsuno, and B. L. McNaughton
Fast-Forward Playback of Recent Memory Sequences in Prefrontal Cortex During Sleep
Science,
November 16, 2007;
318(5853):
1147 - 1150.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Leal-Campanario, A. Fairen, J. M. Delgado-Garcia, and A. Gruart
Electrical stimulation of the rostral medial prefrontal cortex in rabbits inhibits the expression of conditioned eyelid responses but not their acquisition
PNAS,
July 3, 2007;
104(27):
11459 - 11464.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Paz, E. P. Bauer, and D. Pare
Learning-Related Facilitation of Rhinal Interactions by Medial Prefrontal Inputs
J. Neurosci.,
June 13, 2007;
27(24):
6542 - 6551.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|