Sex- and hormone-dependent alterations in alcohol withdrawal-induced anxiety and corticolimbic endocannabinoid signaling

被引:33
作者
Henricks, Angela M. [1 ]
Berger, Anthony L. [1 ]
Lugo, Janelle M. [2 ]
Baxter-Potter, Lydia N. [2 ]
Bieniasz, Kennedy V. [2 ]
Petrie, Gavin [4 ,5 ]
Sticht, Martin A. [4 ,5 ]
Hill, Matthew N. [4 ,5 ]
McLaughlin, Ryan J. [1 ,2 ,3 ]
机构
[1] Washington State Univ, Dept Psychol, Pullman, WA 99164 USA
[2] Washington State Univ, Dept Integrat Physiol & Neurosci, Pullman, WA 99164 USA
[3] Washington State Univ, Translat Addict Res Ctr, Pullman, WA 99164 USA
[4] Univ Calgary, Hotchkiss Brain Inst, Dept Cell Biol, Calgary, AB, Canada
[5] Univ Calgary, Hotchkiss Brain Inst, Dept Psychiat & Anat, Calgary, AB, Canada
基金
加拿大健康研究院;
关键词
Alcohol; Endocannabinoids; Sex differences; Anxiety; Amygdala; Prefrontal cortex; CHRONIC ETHANOL EXPOSURE; CORTICOTROPIN-RELEASING-FACTOR; CANNABINOID CB1 RECEPTORS; PITUITARY-ADRENAL AXIS; ULTRASONIC VOCALIZATIONS; ANANDAMIDE HYDROLYSIS; BASOLATERAL AMYGDALA; PREFRONTAL CORTEX; GONADAL-HORMONES; CHRONIC STRESS;
D O I
10.1016/j.neuropharm.2017.05.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alcohol dependence is associated with anxiety during withdrawal. The endocannabinoid (ECB) system participates in the neuroendocrine and behavioral response to stress and changes in corticolimbic ECB signaling may contribute to alcohol withdrawal-induced anxiety. Moreover, symptoms of alcohol withdrawal differ between sexes and sexual dimorphism in withdrawal-induced ECB recruitment may be a contributing factor. Herein, we exposed intact male and female rats and ovariectomized (OVX) female rats with or without estradiol (E-2) replacement to 6 weeks of chronic intermittent alcohol vapor and measured anxiety-like behavior, ECB content, and ECB-related mRNA in the basolateral amygdala (BLA) and ventromedial prefrontal cortex (vmPFC). Acute alcohol withdrawal increased anxiety-like behavior, produced widespread disturbances in ECB-related mRNA, and reduced anandamide (AEA) content in the BLA and 2-arachidonoylglycerol (2-AG) content in the vmPFC of male, but not female rats. Similar to males, alcohol-exposed OVX females showed reductions in Napepld mRNA in the BLA, decreased AEA content in the BLA and vmPFC, and reductions in all ECB-related genes measured in the vmPFC. Importantly, E-2 replacement prevented withdrawal-induced alterations in ECB content (but not mRNA) in OVX females, and although alcohol-exposed OVX females failed to exhibit more anxiety compared to their respective control, chronic alcohol exposure abolished the anxiolytic properties of E-2 in OVX rats. These data indicate that ovarian sex hormones (but not E-2 alone) protect against withdrawal-induced alterations in corticolimbic ECB signaling but do not impart resilience to withdrawal-induced anxiety. Thus, the mechanisms implicated in the manifestation of alcohol withdrawal-induced anxiety are most likely sex-specific. This article is part of the Special Issue entitled "A New Dawn in Cannabinoid Neurobiology". Published by Elsevier Ltd.
引用
收藏
页码:121 / 133
页数:13
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