Suppr超能文献

乙醇摄入:我们应该如何测量它?在人类和动物表型之间实现一致。

Ethanol consumption: how should we measure it? Achieving consilience between human and animal phenotypes.

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.

出版信息

Addict Biol. 2010 Apr;15(2):109-24. doi: 10.1111/j.1369-1600.2009.00192.x.

Abstract

There is only modest overlap in the most common alcohol consumption phenotypes measured in animal studies and those typically studied in humans. To address this issue, we identified a number of alcohol consumption phenotypes of importance to the field that have potential for consilience between human and animal models. These phenotypes can be broken down into three categories: (1) abstinence/the decision to drink or abstain; (2) the actual amount of alcohol consumed; and (3) heavy drinking. A number of suggestions for human and animal researchers are made in order to address these phenotypes and enhance consilience. Laboratory studies of the decision to drink or to abstain are needed in both human and animal research. In human laboratory studies, heavy or binge drinking that meets cut-offs used in epidemiological and clinical studies should be reported. Greater attention to patterns of drinking over time is needed in both animal and human studies. Individual differences pertaining to all consumption phenotypes should be addressed in animal research. Lastly, improved biomarkers need to be developed in future research for use with both humans and animals. Greater precision in estimating blood alcohol levels in the field, together with consistent measurement of breath/blood alcohol levels in human laboratory and animal studies, provides one means of achieving greater consilience of alcohol consumption phenotypes.

摘要

在动物研究中测量的最常见的酒精消费表型与通常在人类中研究的表型之间只有适度的重叠。为了解决这个问题,我们确定了一些对该领域很重要的酒精消费表型,这些表型有可能在人类和动物模型之间产生一致性。这些表型可以分为三类:(1) 禁欲/决定饮酒或禁欲;(2) 实际饮酒量;和 (3) 酗酒。为了解决这些表型并增强一致性,我们向人类和动物研究人员提出了一些建议。在人类和动物研究中都需要进行关于决定饮酒或禁欲的实验室研究。在人类实验室研究中,应报告符合流行病学和临床研究中使用的截止值的重度或 binge 饮酒。在动物和人类研究中,都需要更加关注随时间推移的饮酒模式。动物研究中需要解决与所有消费表型有关的个体差异。最后,未来的研究需要开发出用于人类和动物的改进的生物标志物。在现场更精确地估计血液酒精水平,并在人类实验室和动物研究中一致测量呼吸/血液酒精水平,是实现酒精消费表型一致性的一种手段。

相似文献

1
Ethanol consumption: how should we measure it? Achieving consilience between human and animal phenotypes.
Addict Biol. 2010 Apr;15(2):109-24. doi: 10.1111/j.1369-1600.2009.00192.x.
5
Human and laboratory rodent low response to alcohol: is better consilience possible?
Addict Biol. 2010 Apr;15(2):125-44. doi: 10.1111/j.1369-1600.2009.00191.x.
6
Absence of compulsive drinking phenotype in adult male rats exposed to ethanol in a binge-like pattern during adolescence.
Alcohol. 2019 Sep;79:93-103. doi: 10.1016/j.alcohol.2019.01.006. Epub 2019 Jan 18.
7
Face validity of a pre-clinical model of operant binge drinking: just a question of speed.
Addict Biol. 2019 Jul;24(4):664-675. doi: 10.1111/adb.12631. Epub 2018 Jun 4.
8
Genetic and Pharmacologic Manipulation of TLR4 Has Minimal Impact on Ethanol Consumption in Rodents.
J Neurosci. 2017 Feb 1;37(5):1139-1155. doi: 10.1523/JNEUROSCI.2002-16.2016. Epub 2016 Dec 16.
9
Increased delay discounting tracks with a high ethanol-seeking phenotype and subsequent ethanol seeking but not consumption.
Alcohol Clin Exp Res. 2014 Oct;38(10):2607-14. doi: 10.1111/acer.12523. Epub 2014 Oct 21.
10
Quantitative trait loci for sensitivity to acute ethanol and ethanol consummatory behaviors in rats.
Alcohol. 2018 Feb;66:55-67. doi: 10.1016/j.alcohol.2017.08.002. Epub 2017 Aug 12.

引用本文的文献

6
Chronic paternal alcohol exposures induce dose-dependent changes in offspring craniofacial shape and symmetry.
Front Cell Dev Biol. 2024 Jul 1;12:1415653. doi: 10.3389/fcell.2024.1415653. eCollection 2024.
7
High-intensity drinking and hours spent drinking.
Alcohol Clin Exp Res (Hoboken). 2023 Nov;47(11):2081-2089. doi: 10.1111/acer.15189. Epub 2023 Sep 21.
9
Blood Biomarkers of Alcohol Use: A Scoping Review.
Curr Addict Rep. 2021 Dec;8(4):500-508. doi: 10.1007/s40429-021-00402-7. Epub 2021 Oct 15.
10
A novel monobactam lacking antimicrobial activity, MC-100093, reduces sex-specific ethanol preference and depressive-like behaviors in mice.
Neuropharmacology. 2023 Jul 1;232:109515. doi: 10.1016/j.neuropharm.2023.109515. Epub 2023 Mar 29.

本文引用的文献

1
"My drink is larger than yours"? A literature review of self-defined drink sizes and standard drinks.
Curr Drug Abuse Rev. 2008 Jun;1(2):162-76. doi: 10.2174/1874473710801020162.
3
Developing a quantitative measure of alcohol consumption for genomic studies on prospective cohorts.
J Stud Alcohol Drugs. 2009 Mar;70(2):157-68. doi: 10.15288/jsad.2009.70.157.
4
Varenicline reduces alcohol self-administration in heavy-drinking smokers.
Biol Psychiatry. 2009 Jul 15;66(2):185-90. doi: 10.1016/j.biopsych.2009.01.029. Epub 2009 Feb 27.
5
A line of mice selected for high blood ethanol concentrations shows drinking in the dark to intoxication.
Biol Psychiatry. 2009 Apr 15;65(8):662-70. doi: 10.1016/j.biopsych.2008.11.002. Epub 2008 Dec 18.
7
Biomarkers for alcohol use and abuse--a summary.
Alcohol Res Health. 2004;28(1):30-7.
9
Drinking typography established by scheduled induction predicts chronic heavy drinking in a monkey model of ethanol self-administration.
Alcohol Clin Exp Res. 2008 Oct;32(10):1824-38. doi: 10.1111/j.1530-0277.2008.00765.x. Epub 2008 Aug 12.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验