Dopaminergic modulation of endocannabinoid-mediated plasticity at GABAergic synapses in the prefrontal cortex

Similar to dopamine (DA), cannabinoids strongly influence prefrontal cortical functions, such as working memory, emotional learning, and sensory perception. Although endogenous cannabinoid receptors (CB(1)Rs) are abundantly expressed in the prefrontal cortex (PFC), very little is known about endocan...

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Veröffentlicht in:The Journal of neuroscience 2010-05, Vol.30 (21), p.7236-7248
Hauptverfasser: Chiu, Chiayu Q, Puente, Nagore, Grandes, Pedro, Castillo, Pablo E
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container_title The Journal of neuroscience
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creator Chiu, Chiayu Q
Puente, Nagore
Grandes, Pedro
Castillo, Pablo E
description Similar to dopamine (DA), cannabinoids strongly influence prefrontal cortical functions, such as working memory, emotional learning, and sensory perception. Although endogenous cannabinoid receptors (CB(1)Rs) are abundantly expressed in the prefrontal cortex (PFC), very little is known about endocannabinoid (eCB) signaling in this brain region. Recent behavioral and electrophysiological evidence has suggested a functional interplay between the dopamine and cannabinoid receptor systems, although the cellular mechanisms underlying this interaction remain to be elucidated. We examined this issue by combining neuroanatomical and electrophysiological techniques in PFC of rats and mice (both genders). Using immunoelectron microscopy, we show that CB(1)Rs and dopamine type 2 receptors (D(2)Rs) colocalize at terminals of symmetrical, presumably GABAergic, synapses in the PFC. Indeed, activation of either receptor can suppress GABA release onto layer 5 pyramidal cells. Furthermore, coactivation of both receptors via repetitive afferent stimulation triggers eCB-mediated long-term depression of inhibitory transmission (I-LTD). This I-LTD is heterosynaptic in nature, requiring glutamate release to activate group I metabotropic glutamate receptors. D(2)Rs most likely facilitate eCB signaling at the presynaptic site as disrupting postsynaptic D(2)R signaling does not diminish I-LTD. Facilitation of eCB-LTD may be one mechanism by which DA modulates neuronal activity in the PFC and regulates PFC-mediated behavior in vivo.
doi_str_mv 10.1523/JNEUROSCI.0736-10.2010
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subjects Animals
Animals, Newborn
Benzoxazines - pharmacology
Cannabinoid Receptor Modulators
Chelating Agents - pharmacology
Dopamine - metabolism
Dopamine Agents - pharmacology
Egtazic Acid - analogs & derivatives
Egtazic Acid - pharmacology
Endocannabinoids
Female
gamma-Aminobutyric Acid - metabolism
In Vitro Techniques
Inhibitory Postsynaptic Potentials - drug effects
Inhibitory Postsynaptic Potentials - genetics
Isoquinolines - pharmacology
Membrane Potentials - drug effects
Mice
Mice, Inbred C57BL
Mice, Knockout
Microscopy, Electron, Transmission - methods
Morpholines - pharmacology
Naphthalenes - pharmacology
Neuronal Plasticity - genetics
Neuronal Plasticity - physiology
Patch-Clamp Techniques
Piperidines - pharmacology
Prefrontal Cortex - cytology
Prefrontal Cortex - ultrastructure
Protein Kinase Inhibitors - pharmacology
Pyrazoles - pharmacology
Rats
Rats, Wistar
Receptor, Cannabinoid, CB1 - agonists
Receptor, Cannabinoid, CB1 - deficiency
Receptor, Cannabinoid, CB1 - metabolism
Receptors, Dopamine D2 - metabolism
Silver Staining - methods
Sulfonamides - pharmacology
Synapses - drug effects
Synapses - physiology
Synapses - ultrastructure
title Dopaminergic modulation of endocannabinoid-mediated plasticity at GABAergic synapses in the prefrontal cortex
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