Rodriguez-Romaguera Jose, Greenberg Benjamin D, Rasmussen Steven A, Quirk Gregory J
Departments of Psychiatry and Anatomy and Neurobiology, University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
Department of Psychiatry and Human Behavior, Brown University, Providence, Rhode Island.
Biol Psychiatry. 2016 Oct 1;80(7):534-40. doi: 10.1016/j.biopsych.2016.02.012. Epub 2016 Feb 17.
Obsessive-compulsive disorder is treated with exposure with response prevention (ERP) therapy, in which patients are repeatedly exposed to compulsive triggers but prevented from expressing their compulsions. Many compulsions are an attempt to avoid perceived dangers, and the intent of ERP is to extinguish compulsions. Patients failing ERP therapy are candidates for deep brain stimulation (DBS) of the ventral capsule/ventral striatum, which facilitates patients' response to ERP therapy. An animal model of ERP would be useful for understanding the neural mechanisms of extinction in obsessive-compulsive disorder.
Using a platform-mediated signaled avoidance task, we developed a rodent model of ERP called extinction with response prevention (Ext-RP), in which avoidance-conditioned rats are given extinction trials while blocking access to the avoidance platform. Following 3 days of Ext-RP, rats were tested with the platform unblocked to evaluate persistent avoidance. We then assessed if pharmacologic inactivation of lateral orbitofrontal cortex (lOFC) or DBS of the ventral striatum reduced persistent avoidance.
Following Ext-RP training, most rats showed reduced avoidance at test (Ext-RP success), but a subset persisted in their avoidance (Ext-RP failure). Pharmacologic inactivation of lOFC eliminated persistent avoidance, as did DBS applied to the ventral striatum during Ext-RP.
DBS of ventral striatum has been previously shown to inhibit lOFC activity. Thus, activity in lOFC, which is known to be hyperactive in obsessive-compulsive disorder, may be responsible for impairing patients' response to ERP therapy.
强迫症采用暴露与反应阻止疗法(ERP)进行治疗,即让患者反复接触强迫触发因素,但阻止其表现出强迫行为。许多强迫行为是为了避免感知到的危险,而ERP的目的是消除强迫行为。ERP治疗失败的患者是腹侧囊/腹侧纹状体深部脑刺激(DBS)的候选对象,DBS可促进患者对ERP治疗的反应。ERP的动物模型有助于理解强迫症消退的神经机制。
利用平台介导的信号回避任务,我们开发了一种名为消退与反应阻止(Ext-RP)的啮齿动物ERP模型,即对回避条件化的大鼠进行消退试验,同时阻止其进入回避平台。经过3天的Ext-RP训练后,在平台无障碍的情况下对大鼠进行测试,以评估持续回避情况。然后,我们评估外侧眶额皮质(lOFC)的药物失活或腹侧纹状体的DBS是否能减少持续回避行为。
经过Ext-RP训练后,大多数大鼠在测试时回避行为减少(Ext-RP成功),但有一部分大鼠持续表现出回避行为(Ext-RP失败)。lOFC的药物失活消除了持续回避行为,在Ext-RP期间对腹侧纹状体进行DBS也有同样效果。
先前已表明腹侧纹状体的DBS会抑制lOFC的活动。因此,已知在强迫症中过度活跃的lOFC的活动可能是导致患者对ERP治疗反应受损的原因。