Brody Arthur L
Department of Psychiatry and Biobehavioral Sciences, UCLA School of Medicine, 300 UCLA Medical Plaza, Suite 2200, Los Angeles, CA 90095, United States.
J Psychiatr Res. 2006 Aug;40(5):404-18. doi: 10.1016/j.jpsychires.2005.04.012. Epub 2005 Jun 24.
While most cigarette smokers endorse a desire to quit smoking, only about 14% to 49% will achieve abstinence after 6 months or more of treatment. A greater understanding of the effects of smoking on brain function may (in conjunction with other lines of research) result in improved pharmacological (and behavioral) interventions. Many research groups have examined the effects of acute and chronic nicotine/cigarette exposure on brain activity using functional imaging; the purpose of this paper is to synthesize findings from such studies and present a coherent model of brain function in smokers. Responses to acute administration of nicotine/smoking include: a reduction in global brain activity; activation of the prefrontal cortex, thalamus, and visual system; activation of the thalamus and visual cortex during visual cognitive tasks; and increased dopamine (DA) concentration in the ventral striatum/nucleus accumbens. Responses to chronic nicotine/cigarette exposure include decreased monoamine oxidase (MAO) A and B activity in the basal ganglia and a reduction in alpha4beta2 nicotinic acetylcholine receptor (nAChR) availability in the thalamus and putamen. Taken together, these findings indicate that smoking enhances neurotransmission through cortico-basal ganglia-thalamic circuits either by direct stimulation of nAChRs, indirect stimulation via DA release or MAO inhibition, or a combination of these factors. Activation of this circuitry may be responsible for the effects of smoking seen in tobacco dependent subjects, such as improvements in attentional performance, mood, anxiety, and irritability.
虽然大多数吸烟者都表示有戒烟的意愿,但经过6个月或更长时间的治疗后,只有约14%至49%的人能够成功戒烟。对吸烟对脑功能影响的更深入理解(结合其他研究方向)可能会带来更好的药物(和行为)干预措施。许多研究小组使用功能成像技术研究了急性和慢性尼古丁/香烟暴露对大脑活动的影响;本文的目的是综合这些研究的结果,并提出一个吸烟者脑功能的连贯模型。对急性给予尼古丁/吸烟的反应包括:全脑活动减少;前额叶皮质、丘脑和视觉系统激活;视觉认知任务期间丘脑和视觉皮质激活;以及腹侧纹状体/伏隔核中多巴胺(DA)浓度增加。对慢性尼古丁/香烟暴露的反应包括基底神经节中单胺氧化酶(MAO)A和B活性降低,以及丘脑和壳核中α4β2烟碱型乙酰胆碱受体(nAChR)可用性降低。综合来看,这些发现表明吸烟通过直接刺激nAChRs、通过DA释放或MAO抑制间接刺激或这些因素的组合,增强了皮质-基底神经节-丘脑回路的神经传递。该神经回路的激活可能是烟草依赖者中吸烟所产生影响的原因,如注意力表现、情绪、焦虑和易怒情绪的改善。