Lax Elad, Friedman Alexander, Croitoru Ofri, Sudai Einav, Ben-Moshe Hila, Redlus Lior, Sasson Efrat, Blumenfeld-Katzir Tamar, Assaf Yaniv, Yadid Gal
The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
The Leslie & Susan Gonda (Goldschmied) Multidisciplinary Brain Research Center, Bar-Ilan University, Ramat-Gan, Israel.
Neuropharmacology. 2013 Dec;75:246-54. doi: 10.1016/j.neuropharm.2013.06.034. Epub 2013 Jul 24.
Deep brain stimulation (DBS) is an emerging technique for effective, non-pharmacological intervention in the course of neurological and neuropsychiatric diseases. Several brain targets have been suggested as suitable for DBS treatment of drug addiction. Previously, we showed that DBS of the lateral habenula (LHb) can reduce cocaine intake, facilitate extinction and attenuate drug-induced relapse in rats trained to self-administrate cocaine. Herein, we demonstrated that cocaine self-administration dose-dependently decreased connectivity between the LHb and midbrain, as shown by neurodegeneration of the main LHb efferent fiber, the fasciculus retroflexus (FR). FR degeneration, in turn, may have caused lack of response to LHb stimulation in rats trained to self-administer high-dose cocaine (1.5 mg/kg; i.v.). Furthermore, we show that the micro-structural changes caused by cocaine can be non-invasively detected using magnetic resonance imaging and diffusion tensor imaging. Detection of cocaine-induced alterations in FR anatomy can aid the selection of potential responders to LHb stimulation for treatment of drug addiction.
深部脑刺激(DBS)是一种用于对神经和神经精神疾病进行有效非药物干预的新兴技术。已有多个脑靶点被认为适用于DBS治疗药物成瘾。此前,我们发现对外侧缰核(LHb)进行DBS可减少大鼠可卡因摄入量,促进消退并减轻药物诱导的复吸,这些大鼠经过训练可自行注射可卡因。在此,我们证明,如主要的LHb传出纤维——后屈束(FR)的神经变性所示,可卡因自行注射呈剂量依赖性地降低LHb与中脑之间的连接性。反过来,FR变性可能导致了经过训练自行注射高剂量可卡因(1.5毫克/千克;静脉注射)的大鼠对LHb刺激缺乏反应。此外,我们表明,使用磁共振成像和扩散张量成像可以无创检测可卡因引起的微观结构变化。检测可卡因诱导的FR解剖结构改变有助于选择可能对LHb刺激有反应的药物成瘾治疗对象。