Li Xuan, Wolf Marina E
Behavioral Neuroscience Research Branch, Intramural Research Program, NIDA/NIH/DHHS, Baltimore, MD, USA.
Department of Neuroscience, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Behav Brain Res. 2015 Feb 15;279:240-54. doi: 10.1016/j.bbr.2014.11.018. Epub 2014 Nov 15.
Brain-derived neurotrophic factor (BDNF) has been found to play roles in many types of plasticity including drug addiction. Here, we focus on rodent studies over the past two decades that have demonstrated diverse roles of BDNF in models of cocaine addiction. First, we will provide an overview of studies showing that cocaine exposure alters (and generally increases) BDNF levels in reward-related regions including the ventral tegmental area, nucleus accumbens, prefrontal cortex, and amygdala. Then we will review evidence that BDNF contributes to behavioral changes in animal models of cocaine addiction, focusing on conditioned place preference, behavioral sensitization, maintenance and reinstatement of self-administration, and incubation of cocaine craving. Last, we will review the role of BDNF in synaptic plasticity, particularly as it relates to plasticity of AMPA receptor transmission after cocaine exposure. We conclude that BDNF regulates cocaine-induced behaviors in a highly complex manner that varies depending on the brain region (and even among different cell types within the same brain region), the nature of cocaine exposure, and the "addiction phase" examined (e.g., acquisition vs maintenance; early vs late withdrawal). These complexities make BDNF a daunting therapeutic target for treating cocaine addiction. However, recent clinical evidence suggests that the serum BDNF level may serve as a biomarker in cocaine addicts to predict future relapse, providing an alternative direction for exploring BDNF's potential relevance to treating cocaine addiction.
脑源性神经营养因子(BDNF)已被发现参与包括药物成瘾在内的多种类型的可塑性过程。在此,我们聚焦过去二十年的啮齿动物研究,这些研究表明BDNF在可卡因成瘾模型中发挥着多种作用。首先,我们将概述一些研究,这些研究表明接触可卡因会改变(通常是增加)奖赏相关脑区(包括腹侧被盖区、伏隔核、前额叶皮层和杏仁核)中的BDNF水平。然后,我们将回顾BDNF促成可卡因成瘾动物模型行为变化的证据,重点关注条件性位置偏爱、行为敏化、自我给药行为的维持和复燃,以及可卡因渴求的潜伏期。最后,我们将回顾BDNF在突触可塑性中的作用,特别是其与可卡因暴露后AMPA受体传递可塑性的关系。我们得出结论,BDNF以高度复杂的方式调节可卡因诱导的行为,这种方式因脑区(甚至同一脑区内不同细胞类型之间)、可卡因暴露的性质以及所研究的“成瘾阶段”(例如,获取与维持;早期与晚期戒断)而异。这些复杂性使得BDNF成为治疗可卡因成瘾的一个艰巨的治疗靶点。然而,最近的临床证据表明,血清BDNF水平可能作为可卡因成瘾者未来复发的生物标志物,为探索BDNF与治疗可卡因成瘾潜在相关性提供了一个新方向。