Hippocampal CA3 NMDA receptors are crucial for adaptive timing of trace eyeblink conditioned response

被引:49
作者
Kishimoto, Y
Nakazawa, K
Tonegawa, S
Kirino, Y
Kano, M
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Cellular Neurophysiol, Kanazawa, Ishikawa 9208640, Japan
[2] Univ Tokyo, Sch Pharmaceut Sci, Lab Neurobiophys, Tokyo 1130033, Japan
[3] NIMH, NIH, Bethesda, MD 20892 USA
[4] MIT, Neurosci Res Ctr, Ctr Canc Res,Howard Hughes Med Inst, RIKEN,Picower Ctr Learning & Memory, Cambridge, MA 02139 USA
[5] MIT, Dept Biol, Cambridge, MA 02139 USA
[6] MIT, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
关键词
NMDA receptor; hippocampus; area CA3; eyeblink conditioning; nonspatial associative memory; mouse;
D O I
10.1523/JNEUROSCI.4142-05.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Classical conditioning of the eyeblink reflex is a simple form of associative learning for motor responses. To examine the involvement of hippocampal CA3 NMDA receptors (NRs) in nonspatial associative memory, mice lacking an NR1 subunit selectively in adult CA3 pyramidal cells [CA3-NR1 knock-out (KO) mice] were subjected to eyeblink conditioning paradigms. Mice received paired presentations of an auditory conditioned stimulus (CS) and a periorbital shock unconditioned stimulus (US). With repeated presentation of the CS followed by the US, wild-type mice learned to blink in anticipation of the US before its onset. We first confirmed that wild-type mice require an intact hippocampus in the trace version of eyeblink conditioning in which the CS and US do not overlap, creating a stimulus-free time gap of 500 ms. Under the same condition, CA3-NR1 KO mice successfully acquired conditioned responses (CRs) during the 10 d acquisition sessions, whereas the extinction of CRs was impaired on the first day of extinction sessions. Importantly, CA3-NR1 KO mice were impaired in the formation of an adaptively timed CR during the first five trials in the daily acquisition sessions. The aberrantly timed CR was also observed in the extinction sessions in accordance with the impaired extinction of CRs. These results indicate that CA3-NR1 KO mice are unable to rapidly retrieve adaptive CR timing, suggesting that CA3 NRs play a crucial role in the memory of adaptive CR timing in trace conditioning.
引用
收藏
页码:1562 / 1570
页数:9
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