Neuroscience and Psychiatry Unit, Faculty of Biology, Medicine and Health, University of Manchester, UK.
Department of Biological Sciences, University of Huddersfield, UK.
Addict Biol. 2018 Sep;23(5):1168-1178. doi: 10.1111/adb.12554. Epub 2017 Sep 22.
Relapse after initially successful treatment is a significant problem facing the treatment of opioid dependence. Evidence suggests craving elicited by re-exposure to drug cues may precipitate relapse. Attempts to identify neural biomarkers of cue-elicited craving have yielded inconsistent findings. We aimed to apply a novel continuous functional magnetic resonance imaging technique to follow the minute-to-minute evolution of brain responses, which correlate with the waxing and waning of craving. Newly detoxified male opioid-dependent patients and healthy control participants attended two separate, counterbalanced, functional magnetic resonance imaging scanning sessions during which they viewed a 10-minute video (drug cue or neutral cue) followed by 5 minutes of fixation. Participants rated the intensity of their craving throughout each session. We hypothesized that subcortical/ventral prefrontal cortex (PFC) regions and dorsal PFC regions would show different associations with craving reflecting their putative roles in appetitive processing versus cognitive control. Compared with controls, drug cue (minus neutral cue) video recruited the left amygdala and was temporally correlated with craving. In contrast, dorsal anterior cingulate blood-oxygen-level-dependent signal time course was higher than controls only during a period after cue exposure when craving levels were declining. Against expectations, neither the ventral striatum nor ventral PFC was significantly recruited by drug cue exposure. Findings suggest that the amygdala has a central role in craving, whereas the dorsal anterior cingulate may control craving in treatment-seeking patients. Time course analysis yielded new insights into the neural substrates of craving that could objectively validate development of psychological and pharmacological approaches to sustained abstinence.
在最初成功治疗后复发是阿片类药物依赖治疗面临的一个重大问题。有证据表明,重新接触药物线索引起的渴望可能会引发复发。尝试确定线索诱发的渴望的神经生物标志物产生了不一致的发现。我们旨在应用一种新的连续功能磁共振成像技术来跟踪大脑反应的每分钟演变,这些反应与渴望的增减相关。新戒毒的男性阿片类药物依赖患者和健康对照参与者参加了两个单独的、平衡的功能磁共振成像扫描会议,在会议期间,他们观看了 10 分钟的视频(药物线索或中性线索),然后是 5 分钟的固定。参与者在每次会议期间都对自己的渴望程度进行评分。我们假设,皮质下/腹侧前额叶皮层 (PFC) 区域和背侧 PFC 区域将显示出与渴望不同的关联,反映了它们在食欲加工与认知控制中的潜在作用。与对照组相比,药物线索(减去中性线索)视频招募了左杏仁核,并且与渴望在时间上相关。相比之下,只有在渴望水平下降期间,背侧前扣带皮层的血氧水平依赖信号时间过程才高于对照组。出乎意料的是,药物线索暴露时,腹侧纹状体和腹侧 PFC 都没有明显被招募。研究结果表明,杏仁核在渴望中起着核心作用,而背侧前扣带皮层可能在寻求治疗的患者中控制渴望。时程分析为渴望的神经基质提供了新的见解,这些见解可以客观地验证心理和药理学方法对持续禁欲的发展。