Addicott Merideth A, Oliver Jason A, Joseph McClernon F
Department of Psychiatry and Behavioral Science, Duke University School of Medicine, Durham, NC, 27710, USA.
Duke-University of North Carolina Brain Imaging and Analysis Center (BIAC), Duke University School of Medicine, Durham, NC, 27710, USA.
Psychopharmacology (Berl). 2017 Apr;234(7):1145-1154. doi: 10.1007/s00213-017-4550-8. Epub 2017 Feb 11.
Tobacco has a higher rate of dependence than other drugs of abuse. However, the psychopharmacological effects of nicotine are incongruent with the tenacity of tobacco addiction since nicotine does not produce robust euphoria in humans or self-administration in rodents. A potential explanation is that nicotine amplifies the salience of other stimuli that have some incentive value, which could influence the initiation and persistence of smoking. However, the neural mechanisms of this process are unknown.
One way that nicotine may amplify the salience of other stimuli is by enhancing reward prediction errors. We hypothesized that nicotine would enhance the neural response to unexpected (relative to expected) rewards compared to placebo.
Twenty-three nonsmokers underwent two fMRI scans, following nicotine (1 mg) or placebo administration, while performing an outcome expectation task. In the task, a pair of cues was associated with either a subsequent reward (the image of a $100 bill) or a nonreward (the image of a blurry rectangle). On 20% of trials, the cue was followed by an unexpected outcome.
Although nicotine did not affect the magnitude of prediction errors relative to placebo, nicotine did increase BOLD activation in the anterior insula/inferior frontal gyrus and decrease activation in the caudate across all outcome types (including both rewards and nonrewards).
The insula and caudate could play a role in the initial effects of nicotine in nonsmokers, and these changes in baseline may be the mechanism that underlies how nicotine amplifies the salience of nondrug stimuli.
烟草的成瘾率高于其他滥用药物。然而,尼古丁的精神药理学效应与烟草成瘾的顽固性并不一致,因为尼古丁在人类中不会产生强烈的欣快感,在啮齿动物中也不会引起自我给药行为。一种可能的解释是,尼古丁会增强其他具有一定激励价值的刺激的显著性,这可能会影响吸烟行为的起始和持续。然而,这一过程的神经机制尚不清楚。
尼古丁增强其他刺激显著性的一种方式可能是通过增强奖励预测误差。我们假设,与安慰剂相比,尼古丁会增强对意外(相对于预期)奖励的神经反应。
23名非吸烟者在接受尼古丁(1毫克)或安慰剂给药后,进行了两次功能磁共振成像扫描,同时执行一项结果预期任务。在该任务中,一对线索分别与随后的奖励(一张100美元钞票的图像)或无奖励(一个模糊矩形的图像)相关联。在20%的试验中,线索之后会出现意外结果。
虽然相对于安慰剂,尼古丁并未影响预测误差的大小,但尼古丁确实增加了前脑岛/额下回的血氧水平依赖(BOLD)激活,并降低了所有结果类型(包括奖励和无奖励)下尾状核的激活。
脑岛和尾状核可能在尼古丁对非吸烟者的初始效应中发挥作用,这些基线变化可能是尼古丁增强非药物刺激显著性的潜在机制。