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阿片类物质与饮酒的关联。

Opioid involvement in alcohol drinking.

作者信息

Froehlich J C, Li T K

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis 46202.

出版信息

Ann N Y Acad Sci. 1994 Oct 31;739:156-67. doi: 10.1111/j.1749-6632.1994.tb19817.x.

DOI:10.1111/j.1749-6632.1994.tb19817.x
PMID:7832469
Abstract

A large body of evidence indicates that the endogenous opioid system plays an important role in maintaining alcohol drinking behavior. Evidence is reviewed that indicates that the reinforcing properties of alcohol that lead to continued and repeated bouts of drinking may be due, in part, to alcohol-induced activation of the endogenous opioid system. Much of this evidence is pharmacologic in nature. Blocking the action of endogenous opioid peptides via administration of opioid antagonists significantly attenuates alcohol consumption in animals under a variety of experimental conditions. In clinical trials, opioid receptor antagonists decrease alcohol consumption, relapse rates, subjective high, and alcohol craving in outpatient alcoholics. The potential clinical utility of opioid receptor antagonists in the treatment of alcoholism and alcohol dependence is discussed.

摘要

大量证据表明,内源性阿片系统在维持饮酒行为中起重要作用。本文综述了相关证据,这些证据表明导致持续和反复饮酒发作的酒精强化特性可能部分归因于酒精对内源性阿片系统的激活。其中大部分证据本质上是药理学方面的。在各种实验条件下,通过给予阿片拮抗剂阻断内源性阿片肽的作用可显著减少动物的酒精摄入量。在临床试验中,阿片受体拮抗剂可减少门诊酗酒者的酒精摄入量、复发率、主观兴奋感和对酒精的渴望。本文还讨论了阿片受体拮抗剂在治疗酒精中毒和酒精依赖方面的潜在临床应用。

相似文献

1
Opioid involvement in alcohol drinking.阿片类物质与饮酒的关联。
Ann N Y Acad Sci. 1994 Oct 31;739:156-67. doi: 10.1111/j.1749-6632.1994.tb19817.x.
2
Recent developments in alcoholism:opioid peptides.酒精中毒的最新进展:阿片肽
Recent Dev Alcohol. 1993;11:187-205.
3
Genetics of alcoholism: role of the endogenous opioid system.酒精中毒的遗传学:内源性阿片系统的作用。
Metab Brain Dis. 1994 Jun;9(2):105-31. doi: 10.1007/BF01999765.
4
Influence of the endogenous opioid system on high alcohol consumption and genetic predisposition to alcoholism.内源性阿片系统对高酒精摄入量及酒精成瘾遗传易感性的影响。
J Psychiatry Neurosci. 2001 Sep;26(4):304-18.
5
Interactions between cannabinoid and opioid receptor systems in the mediation of ethanol effects.大麻素与阿片受体系统在介导乙醇效应中的相互作用。
Alcohol Alcohol. 2005 Jan-Feb;40(1):25-34. doi: 10.1093/alcalc/agh112. Epub 2004 Nov 18.
6
Opioids and alcoholism.阿片类药物与酒精成瘾
Physiol Behav. 2004 Apr;81(2):339-58. doi: 10.1016/j.physbeh.2004.02.008.
7
Endogenous opioid systems and alcohol addiction.内源性阿片系统与酒精成瘾。
Psychopharmacology (Berl). 1997 Jan;129(2):99-111. doi: 10.1007/s002130050169.
8
Genetic factors in alcohol self-administration.酒精自我给药中的遗传因素。
J Clin Psychiatry. 1995;56 Suppl 7:15-23.
9
The opioidergic-alcohol link : implications for treatment.阿片类物质与酒精的关联:对治疗的启示
CNS Drugs. 2005;19(8):693-707. doi: 10.2165/00023210-200519080-00005.
10
Ethanol-induced change in cardiac and endogenous opiate function and risk for alcoholism.乙醇引起的心脏和内源性阿片类物质功能变化与酒精中毒风险
Alcohol Clin Exp Res. 1996 Dec;20(9):1542-52. doi: 10.1111/j.1530-0277.1996.tb01697.x.

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Combining naltrexone and prazosin in a single oral medication decreases alcohol drinking more effectively than does either drug alone.将纳曲酮和普萘洛尔结合在单一口服药物中,比单独使用任何一种药物更能有效地减少饮酒量。
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Gestational naltrexone ameliorates fetal ethanol exposures enhancing effect on the postnatal behavioral and neural response to ethanol.妊娠纳曲酮可改善胎儿乙醇暴露对产后乙醇行为和神经反应的增强作用。
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