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The Effect of Chronic Alcohol on Cognitive Decline: Do Variations in Methodology Impact Study Outcome? An Overview of Research From the Past 5 Years.慢性酒精对认知衰退的影响:研究方法的差异会影响研究结果吗?过去5年研究综述
Front Neurosci. 2022 Mar 10;16:836827. doi: 10.3389/fnins.2022.836827. eCollection 2022.
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Alcoholics Anonymous and other 12-step programs for alcohol use disorder.戒酒互助会及其他针对酒精使用障碍的12步康复计划。
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Chronic moderate alcohol drinking alters insulin release without affecting cognitive and emotion-like behaviors in rats.慢性中度饮酒改变胰岛素释放,而不影响大鼠的认知和类情绪行为。
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[Cognitive impairments in alcohol dependence: From screening to treatment improvements].[酒精依赖中的认知障碍:从筛查到治疗改善]
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引用本文的文献

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Int J Mol Sci. 2024 Aug 5;25(15):8526. doi: 10.3390/ijms25158526.
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Chronic alcohol-induced long-lasting working memory deficits are associated with altered histone H3K9 dimethylation in the prefrontal cortex.慢性酒精诱导的长期工作记忆缺陷与前额叶皮质中组蛋白H3K9二甲基化改变有关。
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3
Chronic alcohol consumption shifts learning strategies and synaptic plasticity from hippocampus to striatum-dependent pathways.长期饮酒会使学习策略和突触可塑性从海马体依赖途径转变为纹状体依赖途径。
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4
Lipidomic changes of cerebral cortex in aldehyde dehydrogenase-2 knock-in heterozygote mice after chronic alcohol exposure.慢性酒精暴露后醛脱氢酶-2基因敲入杂合子小鼠大脑皮质的脂质组学变化
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本文引用的文献

1
N-acetylcysteine reduces addiction-like behaviour towards high-fat high-sugar food in diet-induced obese rats.N-乙酰半胱氨酸可减少饮食诱导肥胖大鼠对高脂肪高糖食物的成瘾样行为。
Eur J Neurosci. 2021 Aug;54(3):4877-4887. doi: 10.1111/ejn.15321. Epub 2021 Jun 17.
2
Three Weeks of Binge Alcohol Drinking Generates Increased Alcohol Front-Loading and Robust Compulsive-Like Alcohol Drinking in Male and Female C57BL/6J Mice. binge alcohol drinking 是豪饮 binge drinking 的名词形式,因此,译文“Three Weeks of Binge Alcohol Drinking”可处理为“连续三周豪饮酒精”。此外,原文中的“front-loading”通常被翻译为“前置加载”,但结合语境,这里指的是“饮酒量前置增加”,因此,译文将其处理为“饮酒量前置增加”。 综上,译文为: 连续三周豪饮酒精可导致雄性和雌性 C57BL/6J 小鼠酒精摄入量前置增加和强迫性觅酒行为增强。
Alcohol Clin Exp Res. 2021 Mar;45(3):650-660. doi: 10.1111/acer.14563. Epub 2021 Feb 17.
3
Impact of sex, strain, and age on blood ethanol concentration and behavioral signs of intoxication during ethanol vapor exposure.性别、品系和年龄对乙醇蒸气暴露期间血乙醇浓度和醉酒行为体征的影响。
Neuropharmacology. 2021 Feb 15;184:108393. doi: 10.1016/j.neuropharm.2020.108393. Epub 2020 Nov 19.
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Double-blind, placebo-controlled trial of mifepristone on cognition and depression in alcohol dependence.米非司酮治疗酒精依赖认知和抑郁的双盲、安慰剂对照试验。
Trials. 2020 Sep 16;21(1):796. doi: 10.1186/s13063-020-04726-z.
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7,8-Dihydroxyflavone alleviated the high-fat diet and alcohol-induced memory impairment: behavioral, biochemical and molecular evidence.7,8-二羟基黄酮可缓解高脂饮食和酒精诱导的记忆障碍:行为学、生化和分子证据。
Psychopharmacology (Berl). 2020 Jun;237(6):1827-1840. doi: 10.1007/s00213-020-05502-2. Epub 2020 Mar 23.
6
Kissorphin improves spatial memory and cognitive flexibility impairment induced by ethanol treatment in the Barnes maze task in rats.亲吻素可改善乙醇处理诱导的大鼠巴恩斯迷宫任务中的空间记忆和认知灵活性损伤。
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7
Long-term effects of alcohol consumption on cognitive function: a systematic review and dose-response analysis of evidence published between 2007 and 2018.长期饮酒对认知功能的影响:2007 年至 2018 年期间发表的证据的系统评价和剂量反应分析。
Syst Rev. 2020 Feb 13;9(1):33. doi: 10.1186/s13643-019-1220-4.
8
Behavioral Flexibility in Alcohol-Drinking Monkeys: The Morning After.饮酒猴的行为灵活性:宿醉之后。
Alcohol Clin Exp Res. 2020 Mar;44(3):729-737. doi: 10.1111/acer.14289. Epub 2020 Feb 18.
9
Effects of aminooxyacetic acid on hippocampal mitochondria in rats with chronic alcoholism: the analysis of learning and memory-related genes.氨氧乙酸对慢性酒精中毒大鼠海马线粒体的影响:学习和记忆相关基因分析
J Integr Neurosci. 2019 Dec 30;18(4):451-462. doi: 10.31083/j.jin.2019.04.1119.
10
Chronic voluntary alcohol consumption causes persistent cognitive deficits and cortical cell loss in a rodent model.慢性自愿性饮酒会导致啮齿动物模型中持续的认知缺陷和皮质细胞丢失。
Sci Rep. 2019 Dec 9;9(1):18651. doi: 10.1038/s41598-019-55095-w.

慢性酒精对认知衰退的影响:研究方法的差异会影响研究结果吗?过去5年研究综述

The Effect of Chronic Alcohol on Cognitive Decline: Do Variations in Methodology Impact Study Outcome? An Overview of Research From the Past 5 Years.

作者信息

Charlton Annai J, Perry Christina J

机构信息

Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia.

Florey Department of Neuroscience and Mental Health, University of Melbourne, Parkville, VIC, Australia.

出版信息

Front Neurosci. 2022 Mar 10;16:836827. doi: 10.3389/fnins.2022.836827. eCollection 2022.

DOI:10.3389/fnins.2022.836827
PMID:35360176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8960615/
Abstract

Excessive alcohol use is often associated with accelerated cognitive decline, and extensive research using animal models of human alcohol consumption has been conducted into potential mechanisms for this relationship. Within this literature there is considerable variability in the types of models used. For example, alcohol administration style (voluntary/forced), length and schedule of exposure and abstinence period are often substantially different between studies. In this review, we evaluate recent research into alcohol-induced cognitive decline according to methodology of alcohol access, as well as cognitive behavioral task employed. Our aim was to query whether the nature and severity of deficits observed may be impacted by the schedule and type of alcohol administration. We furthermore examined whether there is any apparent relationship between the amount of alcohol consumed and the severity of the deficit, as well as the potential impact of abstinence length, and other factors such as age of administration, and sex of subject. Over the past five years, researchers have overwhelmingly used non-voluntary methods of intake, however deficits are still found where intake is voluntary. Magnitude of intake and type of task seem most closely related to the likelihood of producing a deficit, however even this did not follow a consistent pattern. We highlight the importance of using systematic and clear reporting styles to facilitate consistency across the literature in this regard. We hope that this analysis will provide important insights into how experimental protocols might influence findings, and how different patterns of consumption are more or less likely to produce an addiction-vulnerable cognitive phenotype in animal models.

摘要

过量饮酒往往与认知能力加速衰退有关,并且已经利用人类饮酒的动物模型对这种关系的潜在机制进行了广泛研究。在这些文献中,所使用模型的类型存在很大差异。例如,酒精给药方式(自愿/强制)、暴露时间和戒酒期的长度和时间表在不同研究之间往往有很大不同。在本综述中,我们根据酒精摄入方法以及所采用的认知行为任务来评估近期关于酒精诱导认知衰退的研究。我们的目的是探究所观察到的缺陷的性质和严重程度是否可能受到酒精给药的时间表和类型的影响。我们还研究了饮酒量与缺陷严重程度之间是否存在明显关系,以及戒酒期长度和其他因素(如给药年龄和受试对象性别)的潜在影响。在过去五年中,研究人员绝大多数使用非自愿摄入方法,然而在自愿摄入的情况下仍发现存在缺陷。摄入量的大小和任务类型似乎与产生缺陷的可能性最密切相关,不过即便如此也没有遵循一致的模式。我们强调使用系统且清晰的报告方式以促进这方面文献一致性的重要性。我们希望这一分析将为实验方案如何影响研究结果以及不同饮酒模式在动物模型中产生成瘾易感性认知表型的可能性大小提供重要见解。