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1
Comparative Overview of Visuospatial Working Memory in Monkeys and Rats.猴子和大鼠视觉空间工作记忆的比较概述
Front Syst Neurosci. 2016 Dec 16;10:99. doi: 10.3389/fnsys.2016.00099. eCollection 2016.
2
Consequences of adolescent use of alcohol and other drugs: Studies using rodent models.青少年使用酒精和其他药物的后果:使用啮齿动物模型的研究。
Neurosci Biobehav Rev. 2016 Nov;70:228-243. doi: 10.1016/j.neubiorev.2016.07.026. Epub 2016 Jul 30.
3
A role for histone acetylation mechanisms in adolescent alcohol exposure-induced deficits in hippocampal brain-derived neurotrophic factor expression and neurogenesis markers in adulthood.组蛋白乙酰化机制在青少年酒精暴露所致成年期海马脑源性神经营养因子表达及神经发生标志物缺陷中的作用。
Brain Struct Funct. 2016 Dec;221(9):4691-4703. doi: 10.1007/s00429-016-1196-y. Epub 2016 Mar 3.
4
Involvement of TLR4 in the long-term epigenetic changes, rewarding and anxiety effects induced by intermittent ethanol treatment in adolescence.TLR4 在青春期间歇性乙醇处理引起的长期表观遗传变化、奖赏和焦虑效应中的作用。
Brain Behav Immun. 2016 Mar;53:159-171. doi: 10.1016/j.bbi.2015.12.006. Epub 2015 Dec 10.
5
Adolescent intermittent alcohol exposure: persistence of structural and functional hippocampal abnormalities into adulthood.青少年间歇性酒精暴露:海马体结构和功能异常持续至成年期。
Alcohol Clin Exp Res. 2015 Jun;39(6):989-97. doi: 10.1111/acer.12725. Epub 2015 Apr 27.
6
Potential role of adolescent alcohol exposure-induced amygdaloid histone modifications in anxiety and alcohol intake during adulthood.青少年酒精暴露诱导的杏仁核组蛋白修饰在成年期焦虑和酒精摄入中的潜在作用。
Neurobiol Dis. 2015 Oct;82:607-619. doi: 10.1016/j.nbd.2015.03.019. Epub 2015 Mar 24.
7
Binge ethanol exposure during adolescence leads to a persistent loss of neurogenesis in the dorsal and ventral hippocampus that is associated with impaired adult cognitive functioning.青春期期间暴饮乙醇会导致背侧和腹侧海马体中神经发生持续丧失,这与成年后认知功能受损有关。
Front Neurosci. 2015 Feb 12;9:35. doi: 10.3389/fnins.2015.00035. eCollection 2015.
8
Consequences of repeated ethanol exposure during early or late adolescence on conditioned taste aversions in rats.青春期早期或晚期反复接触乙醇对大鼠条件性味觉厌恶的影响。
Dev Cogn Neurosci. 2015 Dec;16:174-182. doi: 10.1016/j.dcn.2015.01.004. Epub 2015 Jan 23.
9
Adolescent alcohol exposure: Are there separable vulnerable periods within adolescence?青少年酒精暴露:青春期内是否存在不同的易受影响时期?
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10
Adolescent intermittent ethanol exposure is associated with increased risky choice and decreased dopaminergic and cholinergic neuron markers in adult rats.青春期间歇性乙醇暴露与成年大鼠的风险选择增加以及多巴胺能和胆碱能神经元标志物减少有关。
Int J Neuropsychopharmacol. 2014 Oct 31;18(2):pyu003. doi: 10.1093/ijnp/pyu003.

暴饮对发育中大脑的影响——动物模型

Binge Drinking's Effects on the Developing Brain-Animal Models.

作者信息

Hiller-Sturmhöfel Susanne, Spear Linda Patia

机构信息

Susanne Hiller-Sturmhöfel, Ph.D., is a science writer and editor affiliated with CSR Inc., Arlington, Virginia. Linda Patia Spear, Ph.D., is a distinguished professor, Department of Psychology, State University of New York, and the director of the Developmental Exposure Alcohol Research Center, Binghamton University, Binghamton, New York.

出版信息

Alcohol Res. 2018;39(1):77-86.

PMID:30557150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6104958/
Abstract

Adolescence typically is a time of experimentation, including alcohol use and, particularly, binge drinking. Because the brain is still developing during adolescence, such exposure could have long-lasting effects. Animal models and adolescent intermittent ethanol exposure (AIE) paradigms have been used to help elucidate the consequences of adolescent binge drinking. These studies have identified cognitive deficits, particularly in challenging cognitive tasks, and behavioral alterations such as greater risk preferences, impulsivity, and disinhibition. AIE also is associated with changes in affect when the animals reach adulthood, including increased social anxiety and, sometimes, general anxiety. Animal models have demonstrated that AIE can result in retention of certain alcohol-related adolescent phenotypes (i.e., reduced sensitivity to alcohol's aversive effects and increased sensitivity to alcohol's rewarding effects) into adulthood, which may motivate continued elevated alcohol use. The detrimental effects of adolescent alcohol exposure extend to a diversity of lasting alterations in the brain, including reduced neurogenesis, increased proinflammatory responses, changes in gene expression through epigenetic mechanisms, and alterations in the activities of various neurotransmitter systems. Further exploration of these mechanisms in animal models and humans may lead to improved prevention and intervention efforts.

摘要

青春期通常是一个进行各种尝试的时期,包括饮酒,尤其是酗酒。由于大脑在青春期仍在发育,这种接触可能会产生长期影响。动物模型和青少年间歇性乙醇暴露(AIE)范式已被用于帮助阐明青少年酗酒的后果。这些研究已经确定了认知缺陷,特别是在具有挑战性的认知任务中,以及行为改变,如更高的风险偏好、冲动性和去抑制。AIE还与动物成年后的情绪变化有关,包括社交焦虑增加,有时还有一般性焦虑。动物模型表明,AIE可导致某些与酒精相关的青少年表型(即对酒精厌恶作用的敏感性降低和对酒精奖励作用的敏感性增加)持续到成年期,这可能促使酒精使用持续增加。青少年酒精暴露的有害影响延伸到大脑中多种持久的改变,包括神经发生减少、促炎反应增加、通过表观遗传机制改变基因表达以及各种神经递质系统活动的改变。在动物模型和人类中对这些机制的进一步探索可能会导致预防和干预措施的改进。