Dias Nadeeka R, Schmitz Joy M, Rathnayaka Nuvan, Red Stuart D, Sereno Anne B, Moeller F Gerard, Lane Scott D
The University of Texas Health Science Center at Houston, Department of Psychiatry and Behavioral Sciences, 1941 East Rd, Houston, TX 77054, United States.
The University of Texas Health Science Center at Houston, Department of Psychiatry and Behavioral Sciences, 1941 East Rd, Houston, TX 77054, United States.
Behav Brain Res. 2015 Oct 1;292:493-9. doi: 10.1016/j.bbr.2015.07.006. Epub 2015 Jul 8.
Cocaine-dependent (CD) subjects show attentional bias toward cocaine-related cues, and this form of cue-reactivity may be predictive of craving and relapse. Attentional bias has previously been assessed by models that present drug-relevant stimuli and measure physiological and behavioral reactivity (often reaction time). Studies of several CNS diseases outside of substance use disorders consistently report anti-saccade deficits, suggesting a compromise in the interplay between higher-order cortical processes in voluntary eye control (i.e., anti-saccades) and reflexive saccades driven more by involuntary midbrain perceptual input (i.e., pro-saccades). Here, we describe a novel attentional-bias task developed by using measurements of saccadic eye movements in the presence of cocaine-specific stimuli, combining previously unique research domains to capitalize on their respective experimental and conceptual strengths. CD subjects (N = 46) and healthy controls (N = 41) were tested on blocks of pro-saccade and anti-saccade trials featuring cocaine and neutral stimuli (pictures). Analyses of eye-movement data indicated (1) greater overall anti-saccade errors in the CD group; (2) greater attentional bias in CD subjects as measured by anti-saccade errors to cocaine-specific (relative to neutral) stimuli; and (3) no differences in pro-saccade error rates. Attentional bias was correlated with scores on the obsessive-compulsive cocaine scale. The results demonstrate increased saliency and differential attentional to cocaine cues by the CD group. The assay provides a sensitive index of saccadic (visual inhibitory) control, a specific index of attentional bias to drug-relevant cues, and preliminary insight into the visual circuitry that may contribute to drug-specific cue reactivity.
可卡因依赖(CD)受试者对与可卡因相关的线索表现出注意力偏向,而这种线索反应形式可能预示着渴望和复发。注意力偏向以前是通过呈现与药物相关的刺激并测量生理和行为反应(通常是反应时间)的模型来评估的。对物质使用障碍之外的几种中枢神经系统疾病的研究一致报告了反扫视缺陷,这表明在自愿眼动控制(即反扫视)中的高阶皮质过程与更多由非自愿中脑感知输入驱动的反射性扫视(即顺扫视)之间的相互作用受到了损害。在此,我们描述了一种新颖的注意力偏向任务,该任务通过在存在可卡因特异性刺激的情况下测量眼球跳动来开发,结合了以前独特的研究领域,以利用它们各自的实验和概念优势。对CD受试者(N = 46)和健康对照者(N = 41)进行了以可卡因和中性刺激(图片)为特征的顺扫视和反扫视试验块的测试。眼动数据的分析表明:(1)CD组的总体反扫视错误更多;(2)以对可卡因特异性(相对于中性)刺激的反扫视错误来衡量,CD受试者的注意力偏向更大;(3)顺扫视错误率没有差异。注意力偏向与强迫性可卡因量表上的得分相关。结果表明CD组对可卡因线索的显著性增加且注意力存在差异。该测定提供了眼球跳动(视觉抑制)控制的敏感指标、对与药物相关线索的注意力偏向的特定指标,以及对可能导致药物特异性线索反应的视觉回路的初步见解。