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本文引用的文献

1
Chronic ethanol and withdrawal differentially modulate pre- and postsynaptic function at glutamatergic synapses in rat basolateral amygdala.慢性乙醇及其戒断对大鼠基底外侧杏仁核谷氨酸能突触的突触前和突触后功能有不同的调节作用。
J Neurophysiol. 2007 Dec;98(6):3185-96. doi: 10.1152/jn.00189.2007. Epub 2007 Sep 26.
2
Adolescent cortical development: a critical period of vulnerability for addiction.青少年皮质发育:成瘾易感性的关键时期。
Pharmacol Biochem Behav. 2007 Feb;86(2):189-99. doi: 10.1016/j.pbb.2006.12.001. Epub 2007 Jan 12.
3
A new measure of binge drinking: prevalence and correlates in a probability sample of undergraduates.一种新的暴饮行为衡量方法:本科生概率样本中的患病率及其相关因素
Alcohol Clin Exp Res. 2006 Nov;30(11):1896-905. doi: 10.1111/j.1530-0277.2006.00234.x.
4
Long-term potentiation in the amygdala: a cellular mechanism of fear learning and memory.杏仁核中的长时程增强:恐惧学习与记忆的细胞机制。
Neuropharmacology. 2007 Jan;52(1):215-27. doi: 10.1016/j.neuropharm.2006.06.022. Epub 2006 Aug 21.
5
Repeated withdrawal from ethanol spares contextual fear conditioning and spatial learning but impairs negative patterning and induces over-responding: evidence for effect on frontal cortical but not hippocampal function?反复戒断乙醇可保留情境恐惧条件反射和空间学习能力,但会损害负性模式并引发过度反应:这是对额叶皮质而非海马功能产生影响的证据吗?
Eur J Neurosci. 2006 Jul;24(1):205-16. doi: 10.1111/j.1460-9568.2006.04901.x.
6
Previous experience of ethanol withdrawal increases withdrawal-induced c-fos expression in limbic areas, but not withdrawal-induced anxiety and prevents withdrawal-induced elevations in plasma corticosterone.既往乙醇戒断经历会增加边缘系统区域戒断诱导的c-fos表达,但不会增加戒断诱导的焦虑,且可防止戒断诱导的血浆皮质酮升高。
Psychopharmacology (Berl). 2006 Apr;185(2):188-200. doi: 10.1007/s00213-005-0301-3. Epub 2006 Feb 10.
7
Synaptic mechanisms of associative memory in the amygdala.杏仁核中联想记忆的突触机制。
Neuron. 2005 Sep 15;47(6):783-6. doi: 10.1016/j.neuron.2005.08.009.
8
Neural circuits and mechanisms involved in Pavlovian fear conditioning: a critical review.参与巴甫洛夫恐惧条件反射的神经回路与机制:一项批判性综述。
Neurosci Biobehav Rev. 2006;30(2):188-202. doi: 10.1016/j.neubiorev.2005.06.005. Epub 2005 Aug 24.
9
Chronic ethanol exposure and protracted abstinence alter NMDA receptors in central amygdala.长期乙醇暴露和长期戒酒会改变中央杏仁核中的N-甲基-D-天冬氨酸受体。
Neuropsychopharmacology. 2006 May;31(5):988-96. doi: 10.1038/sj.npp.1300840.
10
Repeated ethanol exposure and withdrawal impairs human fear conditioning and depresses long-term potentiation in rat amygdala and hippocampus.反复接触乙醇并戒断会损害人类恐惧条件反射,并抑制大鼠杏仁核和海马体中的长时程增强效应。
Biol Psychiatry. 2005 Sep 1;58(5):392-400. doi: 10.1016/j.biopsych.2005.04.025.

综述:暴饮的认知和情感后果:杏仁核与前额叶皮质的作用

Review. Cognitive and emotional consequences of binge drinking: role of amygdala and prefrontal cortex.

作者信息

Stephens David N, Duka Theodora

机构信息

Department of Psychology, University of Sussex, Falmer, Brighton, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2008 Oct 12;363(1507):3169-79. doi: 10.1098/rstb.2008.0097.

DOI:10.1098/rstb.2008.0097
PMID:18640918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2607328/
Abstract

Binge drinking is an increasingly recognized problem within the UK. We have studied the relationship of binge drinking to cognitive and emotional functioning in young adults, and have found evidence for increased impulsivity, impairments in spatial working memory and impaired emotional learning. Since in human studies it is difficult to understand whether such behavioural changes pre-date or are a consequence of binge drinking, we have also studied parallel behaviours in a rodent model, in which rats are exposed to intermittent episodes of alcohol consumption and withdrawal. In this model, and in parallel with our findings in human binge drinkers, and alcoholic patients who have undergone multiple episodes of detoxification, we have found evidence for impairments in aversive conditioning as well as increased impulsivity. These behavioural changes are accompanied by facilitated excitatory neurotransmission and reduced plasticity (long-term potentiation (LTP)) in amygdala and hippocampus. The impaired LTP is accompanied by both impaired associative learning and inappropriate generalization of previously learned associations to irrelevant stimuli. We propose that repeated episodes of withdrawal from alcohol induce aberrant neuronal plasticity that results in altered cognitive and emotional competences.

摘要

狂饮在英国已成为一个日益受到关注的问题。我们研究了狂饮与年轻人认知和情绪功能之间的关系,发现了冲动性增加、空间工作记忆受损以及情绪学习障碍的证据。由于在人体研究中很难确定这些行为变化是先于狂饮出现还是狂饮的结果,我们还在啮齿动物模型中研究了类似行为,在该模型中,大鼠会经历间歇性饮酒和戒酒过程。在这个模型中,与我们在人类狂饮者以及经历过多次解毒的酒精性患者中的发现一致,我们发现了厌恶条件反射受损以及冲动性增加的证据。这些行为变化伴随着杏仁核和海马体中兴奋性神经传递的增强以及可塑性降低(长时程增强,LTP)。LTP受损伴随着联想学习受损以及将先前学到的联想不适当地泛化到无关刺激上。我们提出,反复戒酒会诱发异常的神经元可塑性,从而导致认知和情绪能力改变。