Postsynaptic TRPV1 triggers cell type-specific long-term depression in the nucleus accumbens

被引:263
作者
Grueter, Brad A. [1 ]
Brasnjo, Gabor [1 ]
Malenka, Robert C. [1 ]
机构
[1] Stanford Univ, Sch Med, Nancy Pritzker Lab, Dept Psychiat & Behav Sci, Palo Alto, CA 94304 USA
关键词
COCAINE-INDUCED REINSTATEMENT; CENTRAL-NERVOUS-SYSTEM; IN-VIVO EXPOSURE; SYNAPTIC PLASTICITY; BEHAVIORAL SENSITIZATION; RECEPTORS; CHANNELS; ANANDAMIDE; EXPRESSION; ADDICTION;
D O I
10.1038/nn.2685
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptic modifications in the nucleus accumbens (NAc) are important for adaptive and pathological reward-dependent learning. Medium spiny neurons (MSNs), the major cell type in the NAc, participate in two parallel circuits that subserve distinct behavioral functions, yet little is known about differences in their electrophysiological and synaptic properties. Using bacterial artificial chromosome transgenic mice, we found that synaptic activation of group I metabotropic glutamate receptors in NAc MSNs in the indirect, but not direct, pathway led to the production of endocannabinoids, which activated presynaptic CB1 receptors to trigger endocannabinoid-mediated long-term depression (eCB-LTD) as well as postsynaptic transient receptor potential vanilloid 1 (TRPV1) channels to trigger a form of LTD resulting from endocytosis of AMPA receptors. These results reveal a previously unknown action of TRPV1 channels and indicate that the postsynaptic generation of endocannabinoids can modulate synaptic strength in a cell type-specific fashion by activating distinct pre- and postsynaptic targets.
引用
收藏
页码:1519 / U107
页数:8
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