Neurobiology of the nicotine withdrawal syndrome

被引:234
作者
Kenny, PJ [1 ]
Markou, A [1 ]
机构
[1] Scripps Res Inst, Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
关键词
nicotine; drug withdrawal; conditioned place aversion; intracranial self-stimulation; reward; somatic signs; depression; acetylcholine; dopamine; opioid; serotonin; glutamate;
D O I
10.1016/S0091-3057(01)00651-7
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The aversive aspects of withdrawal from chronic nicotine exposure are thought to be an important motivational factor contributing to the maintenance of the tobacco habit in human smokers. Much emphasis has been placed on delineating the underlying neurobiological mechanisms mediating different components of the nicotine withdrawal syndrome. Recent studies have shown that both central and peripheral populations of nicotinic acetylcholine receptors (nAChRs) are involved in mediating somatic signs of nicotine withdrawal as measured by the rodent nicotine abstinence scale. However, only central populations of nAChRs are involved in mediating affective aspects of nicotine withdrawal, as measured by elevations in brain-stimulation reward thresholds and conditioned place aversion. Nicotine interacts with several neurotransmitter systems, including acetylcholine, dopamine, opioid peptides, serotonin, and glutamate systems. Evidence so far suggests that these neurotransmitters play a role in nicotine dependence and withdrawal processes. The available evidence also suggests that different underlying neurochemical deficits mediate somatic and affective components of nicotine withdrawal. The aim of the present review is to discuss preclinical findings concerning the neuroanatomical and neurochemical substrates involved in these different aspects of nicotine withdrawal. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:531 / 549
页数:19
相关论文
共 260 条
[1]  
ABDELRAHMAN ARA, 1989, ARCH INT PHARMACOD T, V297, P68
[2]   DEPRESSION OF MESOLIMBIC DOPAMINE TRANSMISSION AND SENSITIZATION TO MORPHINE DURING OPIATE ABSTINENCE [J].
ACQUAS, E ;
DICHIARA, G .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) :1620-1625
[3]  
Albuquerque EX, 1997, J PHARMACOL EXP THER, V280, P1117
[4]   Nicotine at concentrations found in cigarette smokers activates and desensitizes nicotinic acetylcholine receptors in CA1 interneurons of rat hippocampus [J].
Alkondon, M ;
Pereira, EFR ;
Almeida, LEF ;
Randall, WR ;
Albuquerque, EX .
NEUROPHARMACOLOGY, 2000, 39 (13) :2726-2739
[5]  
Alkondon M, 1997, J PHARMACOL EXP THER, V283, P1396
[6]   The opioid antagonist naltrexone inhibits activity and alters expression of α7 and α4β2 nicotinic receptors in hippocampal neurons:: implications for smoking cessation programs [J].
Almeida, LEF ;
Pereira, EFR ;
Alkondon, M ;
Fawcett, WP ;
Randall, WR ;
Albuquerque, EX .
NEUROPHARMACOLOGY, 2000, 39 (13) :2740-2755
[7]   Neurotrophins and depression [J].
Altar, CA .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1999, 20 (02) :59-61
[8]   CHARACTERIZATION OF N-[H-3]METHYLCARBAMYLCHOLINE BINDING-SITES AND EFFECT OF N-METHYLCARBAMYLCHOLINE ON ACETYLCHOLINE-RELEASE IN RAT-BRAIN [J].
ARAUJO, DM ;
LAPCHAK, PA ;
COLLIER, B ;
QUIRION, R .
JOURNAL OF NEUROCHEMISTRY, 1988, 51 (01) :292-299
[9]  
Arneric Stephen P., 1995, P95
[10]   SWITCHING TO ULTRALOW NICOTINE CIGARETTES - EFFECTS OF DIFFERENT TAR YIELDS AND BLOCKING OF OLFACTORY CUES [J].
BALDINGER, B ;
HASENFRATZ, M ;
BATTIG, K .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1995, 50 (02) :233-239