Committee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, CA 92037, USA.
Committee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, CA 92037, USA.
Front Neuroendocrinol. 2014 Apr;35(2):234-44. doi: 10.1016/j.yfrne.2014.01.001. Epub 2014 Jan 20.
Drug addiction is a chronically relapsing disorder characterized by loss of control over intake and dysregulation of stress-related brain emotional systems. Since the discovery by Wylie Vale and his colleagues of corticotropin-releasing factor (CRF) and the structurally-related urocortins, CRF systems have emerged as mediators of the body's response to stress. Relatedly, CRF systems have a prominent role in driving addiction via actions in the central extended amygdala, producing anxiety-like behavior, reward deficits, excessive, compulsive-like drug self-administration and stress-induced reinstatement of drug seeking. CRF neuron activation in the medial prefrontal cortex may also contribute to the loss of control. Polymorphisms in CRF system molecules are associated with drug use phenotypes in humans, often in interaction with stress history. Drug discovery efforts have yielded brain-penetrant CRF1 antagonists with activity in preclinical models of addiction. The results support the hypothesis that brain CRF-CRF1 systems contribute to the etiology and maintenance of addiction.
药物成瘾是一种慢性复发性疾病,其特征是无法控制摄入量和应激相关大脑情绪系统失调。自 Wylie Vale 及其同事发现促肾上腺皮质释放因子 (CRF) 和结构相关的尿皮质素以来,CRF 系统已成为机体对应激反应的中介。相关地,CRF 系统通过在中央延伸杏仁核中的作用在驱动成瘾方面发挥着突出作用,产生类似焦虑的行为、奖励缺陷、过度、强迫性药物自我给药以及应激引起的觅药行为恢复。内侧前额叶皮质中的 CRF 神经元激活也可能导致无法控制。CRF 系统分子的多态性与人的药物使用表型有关,通常与应激史相互作用。药物发现工作已经产生了具有穿透性的 CRF1 拮抗剂,在成瘾的临床前模型中具有活性。这些结果支持了这样的假设,即大脑 CRF-CRF1 系统有助于成瘾的病因和维持。