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Tribute to: Self-administered nicotine activates the mesolimbic dopamine system through the ventral tegmental area [William Corrigall, Kathleen Coen and Laurel Adamson, Brain Res. 653 (1994) 278-284]
被引:2
|作者:
Leri, Francesco
[1
]
Vaccarino, Franco J.
[1
]
机构:
[1] Univ Guelph, Dept Psychol, Guelph, ON N1G 2W1, Canada
来源:
关键词:
Nicotine;
Self-administration;
Reinforcement;
Ventral tegmental area;
Dopamine;
Pedunculopontine tegmental nucleus;
ACETYLCHOLINE-RECEPTOR SUBUNITS;
INDUCED PLACE PREFERENCE;
CENTRAL-NERVOUS-SYSTEM;
PEDUNCULOPONTINE NUCLEUS;
REINFORCING PROPERTIES;
CHOLINERGIC-RECEPTORS;
LOCOMOTOR-ACTIVITY;
ALCOHOL REWARD;
FIRING PATTERN;
LIMBIC SYSTEM;
D O I:
10.1016/j.brainres.2015.12.064
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
In this paper, Dr. Corrigall and collaborators described elegant experiments designed to elucidate the neurobiology of nicotine reinforcement. The nicotinic receptor antagonist dihydro-beta-erythroidine (DH beta E) was infused in the ventral tegmental area (VTA) or nucleus accumbens (NAC) of rats trained to self-administer nicotine intravenously. Additionally, DH beta E was infused in the VTA of rats trained to self-administer food or cocaine, and nicotine self-administration was assessed in rats with lesions to the peduculopontine tegmental nucleus (PPT). A number of key themes emerged from this fundamental study that remain relevant today. The primary finding was that infusions of DH beta E in the VTA, but not in the NAC, lowered nicotine self-administration, suggesting that nicotinic receptors in VTA are involved in the reinforcing action of nicotine. This conclusion has been confirmed by subsequent findings, and the nature of the nicotinic receptors has also been elucidated. The authors also reported that DH beta E in the VTA had no effect on food or cocaine self-administration, and that lesions to the PPT did not alter nicotine self-administration. Since this initial investigation, the question of whether nicotinic receptors in the VTA are necessary for the reinforcing action of other stimuli, and by which mechanisms, has been extensively explored. Similarly, many groups have further investigated the role of mesopontine cholinergic nuclei in reinforcement. This paper not only contributed in important ways to our understanding of the neurochemical basis of nicotine reinforcement, but was also a key catalyst that gave rise to several research themes central to the neuropharmacology of substance abuse. This article is part of a Special Issue entitled SI:50th Anniversary Issue. (C) 2016 Elsevier B.V. All rights reserved.
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页码:61 / 64
页数:4
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