Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
Ann N Y Acad Sci. 2013 Apr;1282:107-18. doi: 10.1111/nyas.12007. Epub 2013 Feb 11.
Derangements in corticotropin-releasing hormone (CRH) through its type 1 receptor (CRHR1) have been identified in many pathologic conditions. Preclinical models of addiction find that small-molecule antagonists of CRHR1 can limit induction, maintenance, and relapse to drugs of abuse. Neuropsychiatric clinical trials of CRHR1 antagonists have shown mixed efficacy; treatment of addictive disorders has not been established, but finding effective treatments for addictive disorders is critical. Establishing effectiveness for substance abuse treatment will require a different design approach than was used for depression and anxiety trials. Focusing on active versus passive outcome measures, such as resilience to external stressful stimuli, may provide signals in curbing craving and relapse. Study design should include measures of abstinence and drug exposure, but additional elements of stress prevention should also be incorporated. Agents that could provide preemptive protection from drug use and relapse are novel and untested. An understanding of the evolutionary significance of the stress system and preclinical models suggests that these agents may provide protection in this manner. Investigators designing future trials might refocus their understanding of addiction and treatment in this new direction.
促肾上腺皮质激素释放激素 (CRH) 通过其 1 型受体 (CRHR1) 的紊乱已在许多病理状况中被确定。成瘾的临床前模型发现,CRHR1 的小分子拮抗剂可以限制滥用药物的诱导、维持和复发。CRHR1 拮抗剂的神经精神临床研究显示出混合疗效;尚未确定治疗成瘾障碍的方法,但找到有效的成瘾障碍治疗方法至关重要。建立物质滥用治疗的有效性将需要与用于抑郁和焦虑试验的方法不同的设计方法。关注主动与被动的结果测量,例如对外部应激刺激的恢复能力,可能会在遏制渴望和复发方面提供信号。研究设计应包括戒断和药物暴露的测量,但也应纳入压力预防的其他要素。可以提供预防药物使用和复发的预防性保护的药物是新颖且未经测试的。对压力系统的进化意义和临床前模型的理解表明,这些药物可能以这种方式提供保护。设计未来试验的研究人员可能会重新关注他们对成瘾和治疗的理解朝着这个新方向发展。