Literature DB >> 30251377

Nicotine and alcohol: the role of midbrain dopaminergic neurons in drug reinforcement.

Carole Morel1,2,3,4, Sarah Montgomery1,2,3,4, Ming-Hu Han1,2,3,4.   

Abstract

Nicotine and alcohol addiction are leading causes of preventable death worldwide and continue to constitute a huge socio-economic burden. Both nicotine and alcohol perturb the brain's mesocorticolimbic system. Dopamine (DA) neurons projecting from the ventral tegmental area (VTA) to multiple downstream structures, including the nucleus accumbens, prefrontal cortex, and amygdala, are highly involved in the maintenance of healthy brain function. VTA DA neurons play a crucial role in associative learning and reinforcement. Nicotine and alcohol usurp these functions, promoting reinforcement of drug taking behaviors. In this review, we will first describe how nicotine and alcohol individually affect VTA DA neurons by examining how drug exposure alters the heterogeneous VTA microcircuit and network-wide projections. We will also examine how coadministration or previous exposure to nicotine or alcohol may augment the reinforcing effects of the other. Additionally, this review briefly summarizes the role of VTA DA neurons in nicotine, alcohol, and their synergistic effects in reinforcement and also addresses the remaining questions related to the circuit-function specificity of the dopaminergic system in mediating nicotine/alcohol reinforcement and comorbidity.
© 2018 Federation of European Neuroscience Societies and John Wiley & Sons Ltd.

Entities:  

Keywords:  alcohol; circuit; dopamine; electrophysiology; heterogeneity; nicotine; reinforcement; ventral tegmental area

Mesh:

Substances:

Year:  2018        PMID: 30251377      PMCID: PMC6431587          DOI: 10.1111/ejn.14160

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  378 in total

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Authors:  R J Lukas; J P Changeux; N Le Novère; E X Albuquerque; D J Balfour; D K Berg; D Bertrand; V A Chiappinelli; P B Clarke; A C Collins; J A Dani; S R Grady; K J Kellar; J M Lindstrom; M J Marks; M Quik; P W Taylor; S Wonnacott
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