Hanlon Colleen A, Kearney-Ramos Tonisha, Dowdle Logan T, Hamilton Sarah, DeVries William, Mithoefer Oliver, Austelle Christopher, Lench Daniel H, Correia Brittany, Canterberry Melanie, Smith Joshua P, Brady Kathleen T, George Mark S
Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Department of Neurosciences, Medical University of South Carolina, Charleston, SC, USA.
Curr Behav Neurosci Rep. 2017 Dec;4(4):341-352. doi: 10.1007/s40473-017-0135-4. Epub 2017 Oct 23.
Cocaine dependence is a chronic and relapsing disorder which is particularly resistant to behavioral or pharmacologic treatment, and likely involves multiple dysfunctional frontal-striatal circuits. Through advances in preclinical research in the last decade, we now have an unprecedented understanding of the neural control of drug-taking behavior. In both rodent models and human clinical neuroimaging studies, it is apparent that medial frontal-striatal limbic circuits regulate drug cue-triggered behavior. While non-human preclinical studies can use invasive stimulation techniques to inhibit drug cue-evoked behavior, in human clinical neuroscience, we are pursuing non-invasive theta burst stimulation (TBS) as a novel therapeutic tool to inhibit drug cue-associated behavior.
Our laboratory and others have spent the last 7 years systematically and empirically developing a non-invasive, neural circuit-based intervention for cocaine use disorder. Utilizing a multimodal approach of functional brain imaging and brain stimulation, we have attempted to design and optimize a repetitive transcranial magnetic stimulation treatment protocol for cocaine use disorder. This manuscript will briefly review the data largely from our own lab that motivated our selection of candidate neural circuits, and then summarize the results of six studies, culminating in the first double-blinded, sham-controlled clinical trial of TMS as a treatment adjuvant for treatment-engaged cocaine users (10 sessions, medial prefrontal cortex, 110% resting motor threshold, continuous theta burst stimulation, 3600 pulses/session).
The intent of this review is to highlight one example of a systematic path for TMS treatment development in patients. This path is not necessarily optimal, exclusive, or appropriate for every neurologic or psychiatric disease. Rather, it is one example of a reasoned, empirically derived pathway which we hope will serve as scaffolding for future investigators seeking to develop TMS treatment protocols.
可卡因成瘾是一种慢性复发性疾病,对行为或药物治疗具有特殊的抗性,可能涉及多个功能失调的额叶 - 纹状体回路。通过过去十年临床前研究的进展,我们现在对药物摄取行为的神经控制有了前所未有的理解。在啮齿动物模型和人类临床神经影像学研究中,内侧额叶 - 纹状体边缘回路调节药物线索触发的行为这一点很明显。虽然非人类临床前研究可以使用侵入性刺激技术来抑制药物线索诱发的行为,但在人类临床神经科学中,我们正在探索非侵入性theta爆发刺激(TBS)作为一种新型治疗工具来抑制与药物线索相关的行为。
在过去7年里,我们实验室和其他研究团队系统地、基于经验地开发了一种针对可卡因使用障碍的非侵入性、基于神经回路的干预方法。利用功能性脑成像和脑刺激的多模态方法,我们试图设计并优化一种针对可卡因使用障碍的重复经颅磁刺激治疗方案。本手稿将简要回顾主要来自我们自己实验室的数据,这些数据促使我们选择候选神经回路,然后总结六项研究的结果,最终得出第一项双盲、假对照的临床试验结果,该试验将经颅磁刺激(TMS)作为参与治疗的可卡因使用者的治疗辅助手段(10次治疗,内侧前额叶皮质,110%静息运动阈值,连续theta爆发刺激,每次治疗3600个脉冲)。
本综述的目的是突出一个针对患者的TMS治疗开发系统路径的例子。这条路径不一定是最优的、唯一的,也不一定适用于每种神经或精神疾病。相反,它是一条经过推理、基于经验得出的路径的一个例子,我们希望它能为未来寻求开发TMS治疗方案的研究人员提供框架。