Synaptic and intrinsic plasticity in the ventral tegmental area after chronic cocaine.

@article{Francis:2019aa,

title = {Synaptic and intrinsic plasticity in the ventral tegmental area after chronic cocaine.},

author = {Tanner Chase Francis and Stephanie C Gantz and Khaled Moussawi and Antonello Bonci},

url = {https://www.ncbi.nlm.nih.gov/pubmed/30237117},

doi = {10.1016/j.conb.2018.08.013},

issn = {1873-6882 (Electronic); 0959-4388 (Linking)},

year  = {2019},

date = {2019-02-01},

journal = {Curr Opin Neurobiol},

volume = {54},

pages = {66--72},

address = {Intramural Research Program, Synaptic Plasticity Section, National Institute on Drug Abuse, US National Institutes of Health, Baltimore, MD 21224, USA.},

abstract = {Cocaine exposure induces persistent changes in synaptic transmission and intrinsic properties of ventral tegmental area (VTA) dopamine neurons. Despite significant progress in understanding cocaine-induced plasticity, an effective treatment of cocaine addiction is lacking. Chronic cocaine potentiates excitatory and alters inhibitory transmission to dopamine neurons, induces dopamine neuron hyperexcitability, and reduces dopamine release in projection areas. Understanding how intrinsic and synaptic plasticity interact to control dopamine neuron firing and dopamine release could prove useful in the development of new therapeutics. In this review, we examine recent literature discussing cocaine-induced plasticity in the VTA and highlight potential therapeutic interventions.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}