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饮酒社交者在面临危险饮酒风险时,摄入酒精后对压力的生理心理反应。

Psychophysiological responses to stress following alcohol intake in social drinkers who are at risk of hazardous drinking.

机构信息

University of Minnesota Medical School, Duluth, MN 55812, USA.

出版信息

Biol Psychol. 2013 Apr;93(1):9-16. doi: 10.1016/j.biopsycho.2012.12.009. Epub 2013 Jan 8.

DOI:10.1016/j.biopsycho.2012.12.009
PMID:23313460
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3622864/
Abstract

We examined whether social drinkers whose drinking behavior poses a risk for harmful consequences exhibit altered psychobiological responses to stress following moderate alcohol intake. At risk (n=17) and low risk drinkers (n=27), as identified by the Alcohol Use Disorders Identification Test, completed two laboratory stress sessions, one in which they consumed a drink with alcohol and one without alcohol. Subjective and physiological measures were obtained throughout the study. Reported stimulation following alcohol consumption and sedation post-stress on alcohol day were greater than the no alcohol day in at risk drinkers (ps<.05). Low risk drinkers exhibited stress dampening effects on cortisol levels (p<.05). This was not the case among the high risk drinkers. These results indicate that acute alcohol intake may be associated with enhanced subjective and altered hormonal responses to stress in individuals who are at risk for becoming problem drinkers.

摘要

我们研究了那些饮酒行为可能导致不良后果的社交饮酒者,在适度饮酒后,其应激时的心理生物学反应是否会发生变化。根据酒精使用障碍识别测试(Alcohol Use Disorders Identification Test),有风险(n=17)和低风险(n=27)的饮酒者完成了两次实验室应激试验,一次是饮酒,一次是不饮酒。在整个研究过程中,都获得了主观和生理测量数据。与无酒精日相比,在风险饮酒者中,饮酒后和应激后(酒精日)的兴奋感(reported stimulation)和镇静感(sedation)更高(p<.05)。低风险饮酒者的皮质醇水平呈现应激抑制效应(stress dampening effects)(p<.05)。但高风险饮酒者则并非如此。这些结果表明,在可能成为问题饮酒者的个体中,急性饮酒可能与应激时的主观增强和激素反应改变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/cb6e28448bfd/nihms451770f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/6021a7edcd75/nihms451770f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/c17335a4c31f/nihms451770f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/edbfa5a6dec0/nihms451770f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/cb6e28448bfd/nihms451770f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/6021a7edcd75/nihms451770f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/c17335a4c31f/nihms451770f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/edbfa5a6dec0/nihms451770f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5f3/3622864/cb6e28448bfd/nihms451770f4.jpg

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本文引用的文献

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Alcohol Clin Exp Res. 2011 Oct;35(10):1794-803. doi: 10.1111/j.1530-0277.2011.01522.x. Epub 2011 Jul 18.
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Expanding the utility of the Biphasic Alcohol Effects Scale (BAES) and initial psychometric support for the Brief-BAES (B-BAES).扩展双相酒精效应量表(BAES)的效用,并初步支持简短版 BAES(B-BAES)的心理计量学。
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Alcohol-use disorders.酒精使用障碍
Lancet. 2009 Feb 7;373(9662):492-501. doi: 10.1016/S0140-6736(09)60009-X. Epub 2009 Jan 23.
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Ann N Y Acad Sci. 2008 Oct;1141:105-30. doi: 10.1196/annals.1441.030.
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Exploring the link between gender, sensation seeking, and family history of alcoholism in cortisol stress-response dampening.探索性别、寻求刺激与酒精中毒家族史在皮质醇应激反应抑制方面的联系。
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