Addiction and corticotropin-releasing hormone type 1 receptor antagonist medications

被引:7
|
作者
Contoreggi, Carlo [1 ]
Lee, Mary R. [2 ]
Chrousos, George [3 ]
机构
[1] NIDA, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[2] NIAAA, Lab Clin & Translat Studies, NIH, Bethesda, MD USA
[3] Univ Athens, Sch Med, Aghia Sophia Childrens Hosp, GR-11527 Athens, Greece
来源
ADDICTION REVIEWS | 2013年 / 1282卷
关键词
corticotropin-releasing hormone; CRH antagonists; stress; addiction; GENE-EXPRESSION ANALYSIS; CUE-INDUCED DRUG; PSYCHOLOGICAL STRESS; SENSITIVE PERIODS; MAJOR DEPRESSION; BINDING-KINETICS; SUICIDE BRAIN; CRF FAMILY; COCAINE; REINSTATEMENT;
D O I
10.1111/nyas.12007
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
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.
引用
收藏
页码:107 / 118
页数:12
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