http://www.cnr.it/ontology/cnr/individuo/prodotto/ID37754
Endocannabinoids mediate presynaptic inhibition of glutamatergic transmission in rat ventral tegmental area dopamine neurons through activation of CB1 receptors. (Articolo in rivista)
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- Endocannabinoids mediate presynaptic inhibition of glutamatergic transmission in rat ventral tegmental area dopamine neurons through activation of CB1 receptors. (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1523/JNEUROSCI.4503-03.2004 (literal)
- Alternative label
Miriam Melis (1,2); Marco Pistis (1,2); Simona Perra (1,2); Anna Lisa Muntoni (1,3); Giuliano Pillolla (1,2); Gian Luigi Gessa (1,2) (2004)
Endocannabinoids mediate presynaptic inhibition of glutamatergic transmission in rat ventral tegmental area dopamine neurons through activation of CB1 receptors.
in The Journal of neuroscience
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Miriam Melis (1,2); Marco Pistis (1,2); Simona Perra (1,2); Anna Lisa Muntoni (1,3); Giuliano Pillolla (1,2); Gian Luigi Gessa (1,2) (literal)
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- (1) Centre of Excellence, Neurobiology of Addiction, University of Cagliari, Italy
(2) B. B. Brodie Department of Neuroscience, University of Cagliari, Monserrato, Italy
(3) CNR Institute of Neuroscience, Section of Cagliari, Monserrato, Italy (literal)
- Titolo
- Endocannabinoids mediate presynaptic inhibition of glutamatergic transmission in rat ventral tegmental area dopamine neurons through activation of CB1 receptors. (literal)
- Abstract
- The endogenous cannabinoid system has been shown to play a crucial role in controlling neuronal excitability and synaptic transmission.
In this study we investigated the effects of a cannabinoid receptor (CB-R) agonist WIN 55,212-2 (WIN) on excitatory synaptic transmission
in the rat ventral tegmental area (VTA). Whole-cell patch clamp recordings were performed fromVTAdopamine (DA) neurons in an
in vitro slice preparation. WIN reduced both NMDA and AMPA EPSCs, as well as miniature EPSCs (mEPSCs), and increased the pairedpulse
ratio, indicating a presynaptic locus of its action. We also found that WIN-induced effects were dose-dependent and mimicked by
the CB1-R agonist HU210. Furthermore, two CB1-R antagonists, AM281 and SR141716A, blocked WIN-induced effects, suggesting that
WINmodulates excitatory synaptic transmission via activation of CB1-Rs. Our additional finding that both AM281 and SR141716A per se
increased NMDA EPSCs suggests that endogenous cannabinoids, released from depolarized postsynaptic neurons, might act retrogradely
on presynaptic CB1-Rs to suppress glutamate release. Hence, we report that a type of synaptic modulation, previously termed
depolarization-induced suppression of excitation (DSE), is present also in the VTA as a calcium-dependent phenomenon, blocked by
both AM281 and SR141716A, and occluded by WIN. Importantly, DSE was partially blocked by the D2DA antagonist eticlopride and
enhanced by the D2DA agonist quinpirole without changing the presynaptic cannabinoid sensitivity. These results indicate that the two
pathways work in a cooperative manner to release endocannabinoids in the VTA, where they play a role as retrograde messengers for DSE
via CB1-Rs. (literal)
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