• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

“黑暗中饮酒”(DID):一种简单的类似暴饮暴食式酒精摄入的小鼠模型。

"Drinking in the Dark" (DID): a simple mouse model of binge-like alcohol intake.

作者信息

Thiele Todd E, Crabbe John C, Boehm Stephen L

机构信息

Department of Psychology, University of North Carolina, Chapel Hill, North Carolina.

Portland Alcohol Research Center, Department of Behavioral Neuroscience, Oregon Health & Sciences University, and VA Medical Center, Portland, Oregon.

出版信息

Curr Protoc Neurosci. 2014 Jul 1;68:9.49.1-9.49.12. doi: 10.1002/0471142301.ns0949s68.

DOI:10.1002/0471142301.ns0949s68
PMID:24984686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4142649/
Abstract

One of the greatest challenges that scientists face when studying the neurobiology and/or genetics of alcohol (ethanol) consumption is that most preclinical animal models do not voluntarily consume enough ethanol to achieve pharmacologically meaningful blood ethanol concentrations (BECs). Recent rodent models have been developed that promote binge-like levels of ethanol consumption associated with high BECs (i.e., ≥100 mg/dl). This unit describes procedures for an animal model of binge-like ethanol drinking which has come to be called "drinking in the dark" (DID). The "basic" variation of DID involves replacing the water bottle with a bottle containing 20% ethanol for 2 to 4 hr, beginning 3 hr into the dark cycle, on cages of singly-housed C57BL/6J mice. Using this procedure, mice typically consume enough ethanol to achieve BECs >100 mg/dl and to exhibit behavioral evidence of intoxication. An alternative two-bottle (ethanol and water) procedure is also described.

摘要

科学家在研究酒精(乙醇)消费的神经生物学和/或遗传学过程中面临的最大挑战之一是,大多数临床前动物模型不会主动摄入足够的乙醇以达到具有药理学意义的血液乙醇浓度(BEC)。最近已开发出一些啮齿动物模型,这些模型能促进与高BEC(即≥100mg/dl)相关的类似暴饮水平的乙醇消费。本单元描述了一种类似暴饮式乙醇饮用动物模型的程序,该模型已被称为“黑暗中饮用”(DID)。DID的“基本”变体涉及在单笼饲养的C57BL/6J小鼠的笼子中,从黑暗周期开始3小时后,用装有20%乙醇的瓶子替换水瓶2至4小时。使用此程序,小鼠通常会摄入足够的乙醇以达到>100mg/dl的BEC,并表现出中毒的行为迹象。还描述了另一种双瓶(乙醇和水)程序。

相似文献

1
"Drinking in the Dark" (DID): a simple mouse model of binge-like alcohol intake.“黑暗中饮酒”(DID):一种简单的类似暴饮暴食式酒精摄入的小鼠模型。
Curr Protoc Neurosci. 2014 Jul 1;68:9.49.1-9.49.12. doi: 10.1002/0471142301.ns0949s68.
2
"Drinking in the dark" (DID) procedures: a model of binge-like ethanol drinking in non-dependent mice.“暗饮”(DID)程序:一种非依赖型小鼠 binge-like 乙醇饮用量模型。
Alcohol. 2014 May;48(3):235-41. doi: 10.1016/j.alcohol.2013.08.005. Epub 2013 Oct 29.
3
Repeated cycles of binge-like ethanol (EtOH)-drinking in male C57BL/6J mice augments subsequent voluntary EtOH intake but not other dependence-like phenotypes.雄性 C57BL/6J 小鼠反复 binge 样乙醇(EtOH)摄入会增加随后的自愿 EtOH 摄入,但不会增加其他依赖样表型。
Alcohol Clin Exp Res. 2013 Oct;37(10):1688-95. doi: 10.1111/acer.12145. Epub 2013 May 3.
4
Alcohol Binge Drinking and Anxiety-Like Behavior in Socialized Versus Isolated C57BL/6J Mice.社交化与隔离 C57BL/6J 小鼠的酒精 binge 饮酒和类似焦虑行为。
Alcohol Clin Exp Res. 2020 Jan;44(1):244-254. doi: 10.1111/acer.14236. Epub 2019 Dec 3.
5
Bidirectional enantioselective effects of the GABAB receptor agonist baclofen in two mouse models of excessive ethanol consumption.γ-氨基丁酸B(GABAB)受体激动剂巴氯芬在两种过量饮酒小鼠模型中的双向对映体选择性作用。
Alcohol. 2015 Feb;49(1):37-46. doi: 10.1016/j.alcohol.2014.11.005. Epub 2014 Dec 17.
6
Alcohol intake in two different mouse drinking models after recovery from the lipopolysaccharide-induced sickness reaction.脂多糖诱导的疾病反应恢复后,两种不同小鼠饮水模型中的酒精摄入量。
Alcohol. 2017 Dec;65:1-10. doi: 10.1016/j.alcohol.2017.06.002. Epub 2017 Sep 14.
7
Binge ethanol consumption-associated behavioral impairments in male mice using a gelatin-based drinking-in-the dark model.基于明胶的暗箱灌酒模型研究雄性小鼠 binge 型乙醇摄入相关的行为损伤。
Alcohol. 2021 Sep;95:25-36. doi: 10.1016/j.alcohol.2021.05.001. Epub 2021 May 23.
8
The neurobiology of binge-like ethanol drinking: evidence from rodent models. binge 样乙醇摄入的神经生物学:来自啮齿动物模型的证据。
Physiol Behav. 2012 Jun 6;106(3):325-31. doi: 10.1016/j.physbeh.2011.12.026. Epub 2012 Jan 8.
9
"Wired," yet intoxicated: modeling binge caffeine and alcohol co-consumption in the mouse.“兴奋”却又沉醉:建立小鼠咖啡因与酒精共饮的暴饮暴食模型
Alcohol Clin Exp Res. 2014 Aug;38(8):2269-78. doi: 10.1111/acer.12472. Epub 2014 Jun 24.
10
The development, but not expression, of alcohol front-loading in C57BL/6J mice maintained on LabDiet 5001 is abolished by maintenance on Teklad 2920x rodent diet.在喂以 Teklad 2920x 啮齿动物饲料而非 LabDiet 5001 的情况下,C57BL/6J 小鼠的酒精前负荷发展(而非表达)被消除。
Alcohol Clin Exp Res. 2022 Jul;46(7):1321-1330. doi: 10.1111/acer.14876. Epub 2022 Jun 8.

引用本文的文献

1
Decoding the Liver-Heart Axis in Cardiometabolic Diseases.解读心脏代谢疾病中的肝心轴
Circ Res. 2025 May 23;136(11):1335-1362. doi: 10.1161/CIRCRESAHA.125.325492. Epub 2025 May 22.
2
A Selective GSK3β Inhibitor, Tideglusib, Decreases Intermittent Access and Binge Ethanol Self-Administration in C57BL/6J Mice.一种选择性GSK3β抑制剂, Tideglusib,可减少C57BL/6J小鼠的间歇性接触和暴饮乙醇自我给药行为。
Addict Biol. 2025 May;30(5):e70044. doi: 10.1111/adb.70044.
3
Evidence for independent actions of the CRF and ghrelin systems in binge-like alcohol drinking in mice.
促肾上腺皮质激素释放因子(CRF)和胃饥饿素系统在小鼠暴饮样饮酒行为中的独立作用证据。
Prog Neuropsychopharmacol Biol Psychiatry. 2025 Apr 2;138:111341. doi: 10.1016/j.pnpbp.2025.111341. Epub 2025 Mar 24.
4
Synaptic and synchronic impairments in subcortical brain regions associated with early non-cognitive dysfunction in Alzheimer's disease.与阿尔茨海默病早期非认知功能障碍相关的皮质下脑区的突触和同步性损伤。
Neural Regen Res. 2025 Jan 29;21(1):248-64. doi: 10.4103/NRR.NRR-D-24-01052.
5
Sex Differences in Contextual Extinction Learning After Single Binge-Like EtOH Exposure in Adolescent C57BL/6J Mice.青春期C57BL/6J小鼠单次暴饮样乙醇暴露后情境性消退学习中的性别差异
bioRxiv. 2024 Oct 26:2024.10.25.620195. doi: 10.1101/2024.10.25.620195.
6
Temporal differential effects of post-injury alcohol consumption in a mouse model of blast-induced traumatic brain injury.创伤性脑损伤爆炸诱导的小鼠模型中损伤后酒精摄入的时间差异效应。
Neuroscience. 2024 Dec 6;562:239-251. doi: 10.1016/j.neuroscience.2024.10.003. Epub 2024 Oct 5.
7
Dorsomedial striatal AMPA receptor antagonism increases alcohol binge drinking in selectively bred crossed high alcohol preferring mice.背内侧纹状体 AMPA 受体拮抗作用增加选择性繁殖的高酒精偏好小鼠的酒精 binge 饮用量。
Eur J Neurosci. 2024 Nov;60(9):6300-6311. doi: 10.1111/ejn.16555. Epub 2024 Oct 2.
8
GHSR blockade, but not reduction of peripherally circulating ghrelin via β-adrenergic receptor antagonism, decreases binge-like alcohol drinking in mice.胃饥饿素受体阻断而非通过β-肾上腺素能受体拮抗作用降低外周循环胃饥饿素,可减少小鼠的暴饮样饮酒行为。
Mol Psychiatry. 2025 Mar;30(3):1047-1056. doi: 10.1038/s41380-024-02713-3. Epub 2024 Sep 5.
9
Operant ethanol self-administration behaviors do not predict sex differences in continuous access home cage drinking.操作性乙醇自我给药行为无法预测连续接触笼内饮水的性别差异。
Alcohol. 2025 Mar;123:87-99. doi: 10.1016/j.alcohol.2024.08.004. Epub 2024 Aug 31.
10
Sodium Bicarbonate Decreases Alcohol Consumption in Mice.碳酸氢钠可减少小鼠的酒精摄入量。
Int J Mol Sci. 2024 May 3;25(9):5006. doi: 10.3390/ijms25095006.