Endocannabinoid Signaling and Synaptic Function

被引:777
作者
Castillo, Pablo E. [1 ]
Younts, Thomas J. [1 ]
Chavez, Andres E. [1 ]
Hashimotodani, Yuki [1 ]
机构
[1] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10461 USA
基金
日本学术振兴会;
关键词
LONG-TERM DEPRESSION; DIACYLGLYCEROL LIPASE-ALPHA; CB1 CANNABINOID RECEPTOR; TIMING-DEPENDENT PLASTICITY; MOUSE PREFRONTAL CORTEX; KNOCK-OUT MICE; ENDOGENOUS CANNABINOIDS; INHIBITORY SYNAPSES; NUCLEUS-ACCUMBENS; PYRAMIDAL NEURONS;
D O I
10.1016/j.neuron.2012.09.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Endocannabinoids are key modulators of synaptic function. By activating cannabinoid receptors expressed in the central nervous system, these lipid messengers can regulate several neural functions and behaviors. As experimental tools advance, the repertoire of known endocannabinoid-mediated effects at the synapse, and their underlying mechanism, continues to expand. Retrograde signaling is the principal mode by which endocannabinoids mediate short- and long-term forms of plasticity at both excitatory and inhibitory synapses. However, growing evidence suggests that endocannabinoids can also signal in a nonretrograde manner. In addition to mediating synaptic plasticity, the endocannabinoid system is itself subject to plastic changes. Multiple points of interaction with other neuromodulatory and signaling systems have now been identified. In this Review, we focus on new advances in synaptic endocannabinoid signaling in the mammalian brain. The emerging picture not only reinforces endocannabinoids as potent regulators of synaptic function but also reveals that endocannabinoid signaling is mechanistically more complex and diverse than originally thought.
引用
收藏
页码:70 / 81
页数:12
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