Potential substrates for nicotine and alcohol interactions: A focus on the mesocorticolimbic dopamine system

被引:52
|
作者
Doyon, William M. [1 ]
Thomas, Alyse M. [1 ]
Ostroumov, Alexey [1 ]
Dong, Yu [1 ]
Dani, John A. [1 ]
机构
[1] Baylor Coll Med, Ctr Addict, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Nicotine; Alcohol; Dopamine; Drug abuse; Stress; VENTRAL TEGMENTAL AREA; CHRONIC ETHANOL EXPOSURE; CB1 RECEPTOR ANTAGONIST; GABA-CONTAINING NEURONS; RAT NUCLEUS-ACCUMBENS; INDUCED UP-REGULATION; ACETYLCHOLINE-RECEPTORS; NEUROACTIVE STEROIDS; MESOLIMBIC DOPAMINE; SYNAPTIC PLASTICITY;
D O I
10.1016/j.bcp.2013.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epidemiological studies consistently find correlations between nicotine and alcohol use, yet the neural mechanisms underlying their interaction remain largely unknown. Nicotine and alcohol (i.e., ethanol) share many common molecular and cellular targets that provide potential substrates for nicotine-alcohol interactions. These targets for interaction often converge upon the mesocorticolimbic dopamine system, where the link to drug self-administration and reinforcement is well documented. Both nicotine and alcohol activate the mesocorticolimbic dopamine system, producing downstream dopamine signals that promote the drug reinforcement process. While nicotine primarily acts via nicotinic acetylcholine receptors, alcohol acts upon a wider range of receptors and molecular substrates. The complex pharmacological profile of these two drugs generates overlapping responses that ultimately intersect within the mesocorticolimbic dopamine system to promote drug use. Here we will examine overlapping targets between nicotine and alcohol and provide evidence for their interaction. Based on the existing literature, we will also propose some potential targets that have yet to be directly tested. Mechanistic studies that examine nicotine-alcohol interactions would ultimately improve our understanding of the factors that contribute to the associations between nicotine and alcohol use. Published by Elsevier Inc.
引用
收藏
页码:1181 / 1193
页数:13
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