Endocannabinoids at the synapse a decade after the dies mirabilis (29 March 2001): what we still do not know

被引:62
作者
Alger, Bradley E. [1 ,2 ]
机构
[1] Univ Maryland, Sch Med, Program Neurosci, Dept Physiol, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Program Neurosci, Dept Psychiat, Baltimore, MD 21201 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2012年 / 590卷 / 10期
关键词
LONG-TERM DEPRESSION; DEPOLARIZATION-INDUCED SUPPRESSION; PURKINJE CELL SYNAPSES; ENDOGENOUS CANNABINOIDS; METABOTROPIC GLUTAMATE; RETROGRADE INHIBITION; DEPENDENT PLASTICITY; RECEPTORS; ACTIVATION; ANANDAMIDE;
D O I
10.1113/jphysiol.2011.220855
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Endogenous cannabinoids (endocannabinoids, eCBs) are ubiquitous regulators of synaptic transmission in the brain, mediating numerous forms of short- and long-term plasticity, and having strong influences on synapse formation and neurogenesis. Their roles as retrograde messengers that suppress both excitatory and inhibitory transmission are well-established. Yet, despite intensive investigation, many basic aspects of the eCB system are not understood. This brief review highlights recent advances, problems that remain unresolved, and avenues for future exploration. While 2-arachidonoylglycerol (2-AG) is probably the major eCB for intercellular CB1R-dependent signalling, anandamide (AEA) has come to the forefront in several novel contexts, both as a dual endovanilloid/endocannabinoid that regulates synaptic transmission acutely and as the source of a steady eCB tone in hippocampus. Complexities in the cellular processing of 2-AG are receiving renewed attention, as they are increasingly recognized as major determinants of how 2-AG affects cells. Long-standing fundamental issues such as the synthesis pathway for AEA and the molecular mechanism(s) underlying cellular uptake and release of eCBs remain problematical.
引用
收藏
页码:2203 / 2212
页数:10
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