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Corticotropin releasing factor: A key role in the neurobiology of addiction

期刊

FRONTIERS IN NEUROENDOCRINOLOGY
卷 35, 期 2, 页码 234-244

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yfrne.2014.01.001

关键词

Corticotropin-releasing factor or hormone receptor antagonist; CRF or CRH or urocortin 1 or urocortin 2 or urocortin 3; Anxiety disorder; Major depression; Alcohol or ethanol; Drug addiction or alcoholism or alcohol dependence or alcohol use disorder or binge drinking; Acute or protracted withdrawal or abstinence; Treatment or clinical trial; Stress-induced relapse or reinstatement or craving

资金

  1. NIAAA NIH HHS [F32 AA018914, P60 AA006420, R01 AA020608] Funding Source: Medline
  2. NIDDK NIH HHS [P01 DK026741, R01 DK070118] Funding Source: Medline

向作者/读者索取更多资源

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. (C) 2014 Elsevier Inc. All rights reserved.

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