Cocaine inverts rules for synaptic plasticity of glutamate transmission in the ventral tegmental area (original) (raw)
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- Published: 20 February 2011
Nature Neuroscience volume 14, pages 414–416 (2011)Cite this article
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Abstract
The manner in which drug-evoked synaptic plasticity affects reward circuits remains largely elusive. We found that cocaine reduced NMDA receptor excitatory postsynaptic currents and inserted GluA2–lacking AMPA receptors in dopamine neurons of mice. Consequently, a stimulation protocol pairing glutamate release with hyperpolarizing current injections further strengthened synapses after cocaine treatment. Our data suggest that early cocaine-evoked plasticity in the ventral tegmental area inverts the rules for activity-dependent plasticity, eventually leading to addictive behavior.
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Acknowledgements
We thank the members of the Lüscher laboratory as well as M. Frerking and A. Holtmaat for comments on the manuscript and B. Cerutti for help with the statistical analysis. This work is supported by the Swiss National Science Foundation (C.L.), the Systems X initiative of the Swiss Confederation (NeuroChoice, C.L.).
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Authors and Affiliations
- Department of Basic Neurosciences, Medical Faculty, University of Geneva, Geneva, Switzerland
Manuel Mameli, Camilla Bellone, Matthew T C Brown & Christian Lüscher - Institut du Fer à Moulin, UMR-S 839 INSERM/UPMC, Paris, France
Manuel Mameli - Department of Clinical Neurosciences, Clinic of Neurology, Geneva University Hospital, Geneva, Switzerland
Christian Lüscher
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- Manuel Mameli
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Contributions
M.M. carried out all experiments with two–photon laser glutamate uncaging. M.M., M.T.C.B. and C.B. contributed to the long-term plasticity experiments. C.L. designed the study together with M.T.C.B., C.B. and M.M. and wrote the manuscript with the help of all of the authors.
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Correspondence toChristian Lüscher.
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The authors declare no competing financial interests.
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Mameli, M., Bellone, C., Brown, M. et al. Cocaine inverts rules for synaptic plasticity of glutamate transmission in the ventral tegmental area.Nat Neurosci 14, 414–416 (2011). https://doi.org/10.1038/nn.2763
- Received: 18 October 2010
- Accepted: 24 January 2011
- Published: 20 February 2011
- Issue Date: April 2011
- DOI: https://doi.org/10.1038/nn.2763