TY - JOUR
T1 - Diversity of Dopaminergic Neural Circuits in Response to Drug Exposure
AU - Juarez, Barbara
AU - Han, Ming Hu
N1 - Funding Information:
We thank Stacy Ku and Drs Carole Morel, Peter Rudebeck, and Erin S. Calipari for their helpful guidance and review of these topics. This work was supported by the National Institute on Alcohol Abuse and Alcoholism (R01 AA022445, MHH; F31 AA022862, BJ).
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Addictive substances are known to increase dopaminergic signaling in the mesocorticolimbic system. The origin of this dopamine (DA) signaling originates in the ventral tegmental area (VTA), which sends afferents to various targets, including the nucleus accumbens, the medial prefrontal cortex, and the basolateral amygdala. VTA DA neurons mediate stimuli saliency and goal-directed behaviors. These neurons undergo robust drug-induced intrinsic and extrinsic synaptic mechanisms following acute and chronic drug exposure, which are part of brain-wide adaptations that ultimately lead to the transition into a drug-dependent state. Interestingly, recent investigations of the differential subpopulations of VTA DA neurons have revealed projection-specific functional roles in mediating reward, aversion, and stress. It is now critical to view drug-induced neuroadaptations from a circuit-level perspective to gain insight into how differential dopaminergic adaptations and signaling to targets of the mesocorticolimbic system mediates drug reward. This review hopes to describe the projection-specific intrinsic characteristics of these subpopulations, the differential afferent inputs onto these VTA DA neuron subpopulations, and consolidate findings of drug-induced plasticity of VTA DA neurons and highlight the importance of future projection-based studies of this system.
AB - Addictive substances are known to increase dopaminergic signaling in the mesocorticolimbic system. The origin of this dopamine (DA) signaling originates in the ventral tegmental area (VTA), which sends afferents to various targets, including the nucleus accumbens, the medial prefrontal cortex, and the basolateral amygdala. VTA DA neurons mediate stimuli saliency and goal-directed behaviors. These neurons undergo robust drug-induced intrinsic and extrinsic synaptic mechanisms following acute and chronic drug exposure, which are part of brain-wide adaptations that ultimately lead to the transition into a drug-dependent state. Interestingly, recent investigations of the differential subpopulations of VTA DA neurons have revealed projection-specific functional roles in mediating reward, aversion, and stress. It is now critical to view drug-induced neuroadaptations from a circuit-level perspective to gain insight into how differential dopaminergic adaptations and signaling to targets of the mesocorticolimbic system mediates drug reward. This review hopes to describe the projection-specific intrinsic characteristics of these subpopulations, the differential afferent inputs onto these VTA DA neuron subpopulations, and consolidate findings of drug-induced plasticity of VTA DA neurons and highlight the importance of future projection-based studies of this system.
UR - http://www.scopus.com/inward/record.url?scp=84962674329&partnerID=8YFLogxK
U2 - 10.1038/npp.2016.32
DO - 10.1038/npp.2016.32
M3 - Review article
C2 - 26934955
AN - SCOPUS:84962674329
SN - 0893-133X
VL - 41
SP - 2424
EP - 2446
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 10
ER -