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酒精中毒的最新进展:阿片肽

Recent developments in alcoholism:opioid peptides.

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

Recent Dev Alcohol. 1993;11:187-205.

PMID:7901877
Abstract

A large body of evidence indicates that the endogenous opioid system plays an important role in maintaining alcohol drinking behavior. Research is reviewed indicating that the reinforcing properties of alcohol which lead to continued and repeated bouts of drinking are due, in part, to alcohol-induced activation of the endogenous opioid system. Opioid receptor antagonists decrease alcohol craving, alcohol consumption, and loss of control over drinking. The potential of opioid receptor antagonists to improve treatment outcome in comprehensive relapse prevention programs 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。本文综述了相关研究,表明酒精导致持续和反复饮酒发作的强化特性部分归因于酒精对内源性阿片系统的激活。阿片受体拮抗剂可减少对酒精的渴望、酒精摄入量以及饮酒失控。本文还讨论了阿片受体拮抗剂在综合预防复发项目中改善治疗效果的潜力。

相似文献

1
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.
2
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.
3
[Place of the opioid system in biology and treatment of Alcohol Use Disorder].[阿片类系统在酒精使用障碍生物学及治疗中的地位]
Encephale. 2014 Dec;40(6):457-67. doi: 10.1016/j.encep.2014.10.010. Epub 2014 Nov 22.
4
Effect of naltrexone on human alcohol consumption.纳曲酮对人类酒精摄入量的影响。
J Clin Psychiatry. 1995;56 Suppl 7:24-9.
5
Opioid antagonists in the treatment of alcohol dependence: clinical efficacy and prevention of relapse.阿片类拮抗剂在酒精依赖治疗中的应用:临床疗效及预防复发
Alcohol Alcohol. 1996 Mar;31 Suppl 1:77-81.
6
Treatment of alcoholism as a chronic disorder.将酗酒作为一种慢性疾病进行治疗。
EXS. 1994;71:349-59.
7
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.
8
Voluntary alcohol consumption and plasma beta-endorphin levels in alcohol-preferring rats chronically treated with naltrexone.用纳曲酮长期治疗的嗜酒大鼠的自愿饮酒行为和血浆β-内啡肽水平
Physiol Behav. 2008 Mar 18;93(4-5):1005-10. doi: 10.1016/j.physbeh.2008.01.007. Epub 2008 Jan 16.
9
Alcohol consumption is enhanced after naltrexone treatment.纳曲酮治疗后酒精摄入量增加。
Alcohol Clin Exp Res. 2007 Feb;31(2):260-4. doi: 10.1111/j.1530-0277.2006.00313.x.
10
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.

引用本文的文献

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Bupropion, Alone and in Combination with Naltrexone, Blunts Binge-Like Ethanol Drinking and Intake Following Chronic Intermittent Access to Ethanol in Male C57BL/6J Mice.安非他酮单独及与纳曲酮联合使用可抑制雄性 C57BL/6J 小鼠慢性间歇性乙醇摄入后类似 binge 的乙醇饮用量和摄入量。
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Alcohol Drinking and Blood Alcohol Concentration Revisited.饮酒与血液酒精浓度再探。
Alcohol Clin Exp Res. 2018 Feb;42(2):260-269. doi: 10.1111/acer.13549. Epub 2017 Dec 13.
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Combining Varenicline (Chantix) with Naltrexone Decreases Alcohol Drinking More Effectively Than Does Either Drug Alone in a Rodent Model of Alcoholism.
在酒精中毒的啮齿动物模型中,伐尼克兰(畅沛)与纳曲酮联合使用比单独使用任何一种药物更有效地减少酒精摄入。
Alcohol Clin Exp Res. 2016 Sep;40(9):1961-70. doi: 10.1111/acer.13157. Epub 2016 Jul 29.
4
Prazosin + Naltrexone Decreases Alcohol Drinking More Effectively Than Does Either Drug Alone in P Rats with a Protracted History of Extensive Voluntary Alcohol Drinking, Dependence, and Multiple Withdrawals.在有长期大量自愿饮酒、依赖和多次戒断史的P大鼠中,哌唑嗪 + 纳曲酮比单独使用任何一种药物更有效地减少酒精摄入量。
Alcohol Clin Exp Res. 2015 Sep;39(9):1832-41. doi: 10.1111/acer.12828. Epub 2015 Aug 11.
5
Evidence that Melanocortin Receptor Agonist Melanotan-II Synergistically Augments the Ability of Naltrexone to Blunt Binge-Like Ethanol Intake in Male C57BL/6J Mice.黑素皮质素受体激动剂黑素otan-II协同增强纳曲酮抑制雄性C57BL/6J小鼠暴饮暴食样乙醇摄入能力的证据。
Alcohol Clin Exp Res. 2015 Aug;39(8):1425-33. doi: 10.1111/acer.12774. Epub 2015 Jun 24.
6
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。
Alcohol Clin Exp Res. 2013 Oct;37(10):1763-70. doi: 10.1111/acer.12148. Epub 2013 Jul 22.
7
Decreased immunoreactivity of the polypeptide precursor pro-opiomelanocortin (POMC) and the prohormone convertase pc1/3 after chronic ethanol exposure in Sprague-Dawley rats.慢性乙醇暴露后 Sprague-Dawley 大鼠多肽前体 pro-opiomelanocortin(POMC)和前激素转化酶 pc1/3 的免疫反应性降低。
Alcohol Clin Exp Res. 2013 Mar;37(3):399-406. doi: 10.1111/j.1530-0277.2012.01951.x. Epub 2012 Oct 10.
8
Ethanol-induced increase of agouti-related protein (AgRP) immunoreactivity in the arcuate nucleus of the hypothalamus of C57BL/6J, but not 129/SvJ, inbred mice.乙醇诱导 C57BL/6J 而非 129/SvJ 近交系小鼠下丘脑弓状核中 Agouti 相关蛋白(AgRP)免疫反应性增加。
Alcohol Clin Exp Res. 2010 Apr;34(4):693-701. doi: 10.1111/j.1530-0277.2009.01138.x. Epub 2010 Jan 26.
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The neurobiology of alcoholism in genetically selected rat models.基因选择大鼠模型中的酒精中毒神经生物学
Alcohol Health Res World. 1997;21(2):169-76.
10
Opioid peptides.阿片肽
Alcohol Health Res World. 1997;21(2):132-6.