In Vivo Cocaine Experience Generates Silent Synapses

被引:207
作者
Huang, Yanhua H. [1 ]
Lin, Ying [2 ]
Mu, Ping [1 ]
Lee, Brian R. [1 ]
Brown, Travis E. [1 ]
Wayman, Gary [1 ]
Marie, Helene [3 ]
Liu, Wenhua [4 ]
Yan, Zhen [4 ]
Sorg, Barbara A. [1 ]
Schlueter, Oliver M. [5 ]
Zukin, R. Suzanne [2 ]
Dong, Yan [1 ]
机构
[1] Washington State Univ, Program Neurosci, Pullman, WA 99164 USA
[2] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10461 USA
[3] European Brain Res Inst, I-00143 Rome, Italy
[4] SUNY Buffalo, Dept Physiol, Buffalo, NY 14214 USA
[5] European Neurosci Inst, Dept Mol Neurobiol, D-37077 Gottingen, Germany
关键词
LONG-TERM POTENTIATION; NUCLEUS-ACCUMBENS NEURONS; VENTRAL TEGMENTAL AREA; NMDA RECEPTOR; BEHAVIORAL SENSITIZATION; SYNAPTIC PLASTICITY; AMPA RECEPTORS; EXPRESSION; LTP; MECHANISMS;
D O I
10.1016/j.neuron.2009.06.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Studies over the past decade have enunciated silent synapses as prominent cellular substrates for synaptic plasticity in the developing brain. However, little is known about whether silent synapses can be generated postdevelopmentally. Here, we demonstrate that highly salient in vivo experience, such as exposure to cocaine, generates silent synapses in the nucleus accumbens (NAc) shell, a key brain region mediating addiction-related learning and memory. Furthermore, this cocaine-induced generation of silent synapses is mediated by membrane insertions of new, NR2B-containing N-methyl-D-aspartic acid receptors (NMDARs). These results provide evidence that silent synapses can be generated de novo by in vivo experience and thus may act as highly efficient neural substrates for the subsequent experience-dependent synaptic plasticity underlying extremely long-lasting memory.
引用
收藏
页码:40 / 47
页数:8
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