Endogenous cannabinoids mediate long-term synaptic depression in the nucleus accumbens
Author(s) -
David Robbe,
Manfred Köpf,
Anne Rémaury,
Joël Bockaert,
Olivier J. Manzoni
Publication year - 2002
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.122149199
Subject(s) - long term depression , metabotropic glutamate receptor , neuroscience , synaptic plasticity , nucleus accumbens , neurotransmission , glutamatergic , postsynaptic potential , endocannabinoid system , metaplasticity , synaptic fatigue , glutamate receptor , synaptic augmentation , cannabinoid receptor , retrograde signaling , biology , chemistry , excitatory postsynaptic potential , ampa receptor , receptor , microbiology and biotechnology , central nervous system , inhibitory postsynaptic potential , signal transduction , biochemistry , agonist
Do endocannabinoids (eCBs) participate in long-term synaptic plasticity in the brain? Using pharmacological approaches and genetically altered mice, we show that stimulation of prelimbic cortex afferents at naturally occurring frequencies causes a long-term depression of nucleus accumbens glutamatergic synapses mediated by eCB release and presynaptic CB1 receptors. Translation of glutamate synaptic transmission into eCB retrograde signaling involved metabotropic glutamate receptors and postsynaptic intracellular Ca(2+) stores. These findings unveil the role of the eCB system in activity-dependent long-term synaptic plasticity and identify a mechanism by which marijuana can alter synaptic functions in the endogenous brain reward system.
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