Neurobiology of comorbid post-traumatic stress disorder and alcohol-use disorder

被引:102
|
作者
Gilpin, N. W. [1 ,2 ]
Weiner, J. L. [3 ]
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Physiol, 1901 Perdido St, New Orleans, LA 70112 USA
[2] Louisiana State Univ, Neurosci Ctr Excellence, Hlth Sci Ctr, New Orleans, LA USA
[3] Wake Forest Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC USA
关键词
Alcohol dependence; alcohol use disorder (AUD); alcoholism; post-traumatic stress disorder (PTSD); comorbid PTSD and AUD; amygdala; mesolimbic reward circuit; prefrontal cortex; hippocampus; norepinephrine; SUBSTANCE USE DISORDERS; ANXIETY-LIKE BEHAVIOR; CORTICOTROPIN-RELEASING-FACTOR; NATIONAL EPIDEMIOLOGIC SURVEY; ADOLESCENT SOCIAL-ISOLATION; NUCLEUS-ACCUMBENS DOPAMINE; MEDIAL PREFRONTAL CORTEX; PITUITARY-ADRENAL AXIS; VOLUNTARY ETHANOL-CONSUMPTION; SMALLER HIPPOCAMPAL VOLUME;
D O I
10.1111/gbb.12349
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Post-traumatic stress disorder (PTSD) and alcohol-use disorder (AUD) are highly comorbid in humans. Although we have some understanding of the structural and functional brain changes that define each of these disorders, and how those changes contribute to the behavioral symptoms that define them, little is known about the neurobiology of comorbid PTSD and AUD, which may be due in part to a scarcity of adequate animal models for examining this research question. The goal of this review is to summarize the current state-of-the-science on comorbid PTSD and AUD. We summarize epidemiological data documenting the prevalence of this comorbidity, review what is known about the potential neurobiological basis for the frequent co-occurrence of PTSD and AUD and discuss successes and failures of past and current treatment strategies. We also review animal models that aim to examine comorbid PTSD and AUD, highlighting where the models parallel the human condition, and we discuss the strengths and weaknesses of each model. We conclude by discussing key gaps in our knowledge and strategies for addressing them: in particular, we (1) highlight the need for better animal models of the comorbid condition and better clinical trial design, (2) emphasize the need for examination of subpopulation effects and individual differences and (3) urge cross-talk between basic and clinical researchers that is reflected in collaborative work with forward and reverse translational impact.
引用
收藏
页码:15 / 43
页数:29
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