A line of mice selected for high blood ethanol concentrations shows drinking in the dark to intoxication.
- Authors
- Crabbe, John C; Metten, Pamela; Rhodes, Justin S; Yu, Chia-Hua; Brown, Lauren Lyon; Phillips, Tamara J; Finn, Deborah A
- Year
- 2009
- Journal
- Biological psychiatry
- PMID
- 19095222
- DOI
- 10.1016/j.biopsych.2008.11.002
- PMCID
- PMC3330756
BACKGROUND: Many animal models of alcoholism have targeted aspects of excessive alcohol intake (abuse) and dependence. In the rodent, models aimed at increasing alcohol self-administration have used genetic or environmental manipulations, or their combination. Strictly genetic manipulations (e.g., comparison of inbred strains or targeted mutants, selective breeding) have not yielded rat or mouse genotypes that will regularly and voluntarily drink alcohol to the point of intoxication. Although some behavioral manipulations (e.g., scheduling or limiting access to alcohol, adding a sweetener) will induce mice or rats to drink enough alcohol to become intoxicated, these typically require significant food or water restriction or a long time to develop. We report progress toward the development of a new genetic animal model for high levels of alcohol drinking. METHODS: High Drinking in the Dark (HDID-1) mice have been selectively bred for high blood ethanol concentrations (BEC, ideally exceeding 100 mg%) resulting from the ingestion of a 20% alcohol solution. RESULTS: After 11 generations of selection, more than 56% of the population now exceeds this BEC after a 4-hour drinking session in which a single bottle containing 20% ethanol is available. The dose of ethanol consumed also produced quantifiable signs of intoxication. CONCLUSIONS: These mice will be useful for mechanistic studies of the biological and genetic contributions to excessive drinking.
Response to selection for high blood ethanol concentration (BEC) across 11 selected generations in High Drinking in the Dark (HDID-1) mice. (A) Mean Β± SEM BEC is shown. Solid circles represent the total population tested each generation. Open inverted triangles give values of the animals chosen as parents from the preceding generation: their offspring are represented in solid circles directly below. For numbers of mice, see Table 1. (B) Corresponding ethanol intake (g/kg) for the mice depicted in panel A is shown. (C) Increase in the frequency of HDID-1 subjects with BEC > 1.0 mg/mL across generations is shown. Solid circles depict females, inverted triangles depict males.
Realized response to selection in High Drinking in the Dark (HDID-1) mice. Total realized response to selection in each generation (R) is plotted versus the cumulative selection differential (S) at that generation. RN is the difference between population mean BEC at the Nth generation and mean BEC in generation S0. S is the difference between BEC of individuals selected as parents and the population from which they were selected (see Figure 1A, Table 1). Thus, for example, as described in the text, the mean BEC of generation S4 was .43, whereas that of the foundation population was .30 (see Table 1). The fourth dot from the left depicts R4, the total realized response to selection for S0βS4, as .13 mg/mL. The values for S can be estimated from Figure 1A as the difference between the SN parents (inverted open triangle) minus the SN population mean (black dot), or [(.97β.30) = .67] for S0. This value is added to [(.78 β.32) = .46], [(.77β.37) = .40], [(1.09 β.60) = .49] to obtain cumulated S4 = 2.02. This value appears on the Γ axis for generation S4. The linear regression of R on cumulative S values is shown. From the slope of this line, heritability is estimated to be h2 = .096. Data from males and females were combined for this estimate and are given in Table 1. Units for both axes are in mg EtOH/ml blood, but axes of R on S plots are usually not labeled as such by convention. As explained in Supplement 1, the goodness of fit to a linear regression (r = .91, p < .0001) is an indication that additive genetic variability has not yet been exhausted by selective pressure and that the line will continue to show increased response. Once additive variability begins to diminish significantly, the R/S plot will begin to flatten as it reaches an asymptote, and this method of estimating heritability will no longer be valid.
Increase in intake from S0 to S11 in High Drinking in the Dark mice. Each bar represents the mean Β± SEM ethanol intake (g/kg) during the 2-hour drinking in the dark (DID; Day 1) and the first and last 2 hours of the 4-hour DID test on Day 2. Inset gives key. Data for all generations for total intake on Day 2 are provided in Table 1. For statistical analyses, see Results.
Blood ethanol concentration (BEC) at the end of drinking in the dark testing displayed versus ethanol intake in 163 High Drinking in the Dark mice from generation S11. Individual BECs are plotted versus intake during hours 2β4 (left panel) or hours 0β4 (right panel). Data from males and females are combined, and the linear regression lines are depicted.
Blood ethanol concentration (BEC) at four time points after 2g/kg ethanol (intraperitoneal) in High Drinking in the Dark (HDID-1) mice from S11 and HS/Npt mice. Closed circles depict HS/Npt mice. Open circles depict HDID-1 mice. Symbols and y-error bars represent the mean Β± SEM BEC for each group at each time point. For statistical comparisons, see Results.
Comparison of intake and blood ethanol concentration (BEC) in High Drinking in the Dark mice from S9 with a single-bottle or two-bottle tests (see inset key). Closed circles depict mice tested with a single ethanol tube (standard drinking in the dark [DID] test) and the linear regression of their BEC on their intake (solid line). Open circles depict mice also offered a tube containing water, with a dashed line reflecting the linear regression of their BEC and intake. Symbols with x- and y-error bars represent the mean Β± SEM intake and BEC for each group. For statistical comparisons, see Results.
Intoxication on the balance beam in High Drinking in the Dark mice following drinking in the dark testing. Mean Β± SEM foot slip errors are shown for mice offered ethanol versus those offered water (Control). For statistical comparisons, see Results.
Intoxication on the accelerating rotarod in High Drinking in the Dark mice following drinking in the dark testing in groups offered ethanol versus water. The improvement in rotarod performance is given as the increase in latency to fall (sec) between the third and first trial. Mice tested first on the balance beam are shown in the left panel, and those tested first on the rotarod on the right. For statistical comparisons, see Results.
| Name | Type |
|---|---|
| 20% ethanol solution local | drug |
| Accelerating rotarod local | phenotype |
| alcohol | phenotype |
| alcohol dependence | phenotype |
| Alcoholic drinking local | phenotype |
| Alcohol intake (final 2 hours) local | phenotype |
| alcohol intoxication | phenotype |
| alcohol-related phenotypes | phenotype |
| Alcohol Use | phenotype |
| Balance beam local | phenotype |
| Balance beam performance local | phenotype |
| BECs | phenotype |
| binge drinking episodes | phenotype |
| blood alcohol levels | phenotype |
| blood ethanol concentration | phenotype |
| body weight | phenotype |
| C57BL/6J | cohort |
| circadian dark local | phenotype |
| control group | cohort |
| DID model local | cohort |
| DID test local | phenotype |
| DID test (two-bottle preference version) local | phenotype |
| drinking in the dark | phenotype |
| Drinking in the Dark test local | cohort |
| Ethanol (20% v/v) local | drug |
| ethanol consumption | phenotype |
| ethanol preference drinking local | phenotype |
| excessive alcohol consumption | phenotype |
| first litters of HDID-1 mice local | cohort |
| fluid consumption local | phenotype |
| foot slips local | phenotype |
| Foundational population local | cohort |
| foundation population local | cohort |
| Generation 9 (S9) local | cohort |
| Generation S0 local | cohort |
| Generation S1 local | cohort |
| Generation S11 local | cohort |
| Generation S2 local | cohort |
| HDID-1 local | cohort |
| HDID-1 line local | cohort |
| HDID-1 mice local | cohort |
| HDID-1 mouse local | cohort |
| HDID-2 local | cohort |
| HDID-2 mice local | cohort |
| HDID phenotype local | phenotype |
| high DID local | phenotype |
| higher BEC local | phenotype |
| higher intake local | phenotype |
| higher rotarod performance local | phenotype |
| high intake lines local | cohort |
| HS/Npt | cohort |
| HS/Npt mice local | cohort |
| impairment on fixed speed rotarod local | phenotype |
| inbred strains | cohort |
| Inbreeding coefficient local | phenotype |
| INIA-West local | cohort |
| intoxication | phenotype |
| lower BEC local | phenotype |
| lower intake local | phenotype |
| lower rotarod performance local | phenotype |
| maximal intakes local | phenotype |
| mice | cohort |
| mouse parvo virus local | drug |
| Naive HDID-1 mice local | cohort |
| Naive male mice (second litters, S9 generation) local | cohort |
| Naive mice local | cohort |
| OHSU local | cohort |
| Periorbital sinus local | anatomy |
| Rotarod performance | phenotype |
| S0 generation local | cohort |
| S0 mice | cohort |
| S1 local | cohort |
| S11 local | cohort |
| S11 generation local | cohort |
| S11 mice local | cohort |
| S2 local | cohort |
| S3 local | cohort |
| S4 generation | cohort |
| S5 local | cohort |
| S5 generation local | cohort |
| S6 local | cohort |
| S6βS11 local | cohort |
| S9 local | cohort |
| S9 generation local | cohort |
| S9 HDID-1 mice local | cohort |
| salt | drug |
| Second litters local | cohort |
| second litters of HDID-1 mice local | cohort |
| selected lines | cohort |
| Selfβintoxication local | phenotype |
| sex | phenotype |
| Single-bottle DID intake local | phenotype |
| single-bottle group local | cohort |
| standard DID local | cohort |
| Standard DID group local | cohort |
| sucrose | drug |
| sucrose preference drinking local | phenotype |
| sweet local | drug |
| taste local | phenotype |
| taste preferences local | phenotype |
| taste sensitivity | phenotype |
| two-bottle choice local | cohort |
| Two-bottle choice DID group local | cohort |
| Two-bottle DID intake local | phenotype |
| two-bottle ethanol preference drinking local | phenotype |
| two-bottle group local | cohort |
| VA | cohort |
| voluntary alcohol consumption | phenotype |
| water | drug |
No uploaded files.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Adaptive Serum Biochemistry Responses to Ethanol Administration in a Mouse Model: Implications for Metabolic Regulation Under Analgesia. | Witek B et al. | β | 2025 | β |
| Age-Dependent Differences in Cerebellar CB1 Receptor Expression and Its Association With Impulsivity and Alcohol Intake in Rats. | GΓ³mez-Villatoro JP et al. | β | 2025 | β |
| Animal Models of Excessive Alcohol Consumption in Rodents. | Becker HC et al. | β | 2025 | β |
| A Selective GSK3Ξ² Inhibitor, Tideglusib, Decreases Intermittent Access and Binge Ethanol Self-Administration in C57BL/6J Mice. | Gottlieb S et al. | β | 2025 | β |
| Effect of acute alcohol consumption in a novel rodent model of decision-making. | Giri A et al. | β | 2025 | β |
| Ethanol Increases Diffuse Amyloid Plaque Load and Impairs Memory in the 5xFAD Mouse Model of Alzheimer's Disease. | Le L et al. | β | 2025 | β |
| Genomic and Behavioral Signatures of Selection for Ethanol Preference from the Heterogeneous Stock Collaborative Cross Mice - The Central Nucleus of the Amygdala. | Anderson JQ et al. | β | 2025 | β |
| Genomic and Behavioral Signatures of Selection for Ethanol Preference from the Heterogeneous Stock Collaborative Cross Mice β The Central Nucleus of the Amygdala | Anderson JQ et al. | β | 2025 | β |
| Modeling Brain Gene Expression in Alcohol Use Disorder with Genetic Animal Models. | Hitzemann R et al. | β | 2025 | β |
| Nucleus accumbens core chemogenetic excitation in male mice and chemogenetic inhibition in female mice reduced ethanol reward. | Chan AE et al. | β | 2025 | β |
| Sex differences in nucleus accumbens circuitry engaged with binge-like ethanol drinking. | Chan AE et al. | β | 2025 | β |
| Voluntary wheel-running reduces harmful drinking in a genetic risk model for drinking to intoxication. | Grigsby K et al. | β | 2025 | β |
| Cholinergic interneurons in the shell region of the nucleus accumbens regulate binge alcohol consumption: A chemogenetic and genetic lesion study. | Sharma R et al. | β | 2024 | β |
| Effects of metformin on binge-like ethanol drinking and adenosine monophosphate kinase signaling in inbred high drinking in the dark line 1 mice. | Grigsby K et al. | β | 2024 | β |
| Forced Abstinence from Volitional Ethanol Intake Drives a Vulnerable Period of Hyperexcitability in BNST-Projecting Insular Cortex Neurons. | Taylor A et al. | β | 2024 | β |
| Sex Differences in Mouse Models of Voluntary Alcohol Drinking and Abstinence-Induced Negative Emotion. | Salazar AL et al. | β | 2024 | β |
| Chemical Genetic Identification of PKC Epsilon Substrates in Mouse Brain. | Dugan MP et al. | β | 2023 | β |
| Cyfip2 allelic variation in C57BL/6J and C57BL/6NJ mice alters free-choice ethanol drinking but not binge-like drinking or wheel-running activity. | Hartmann MC et al. | β | 2023 | β |
| Development and implementation of a Dependable, Simple, and Cost-effective (DSC), open-source running wheel in High Drinking in the Dark and Heterogeneous Stock/Northport mice. | Grigsby K et al. | β | 2023 | β |
| Longitudinal assessment of strength and body composition in a mouse model of chronic alcohol-related myopathy. | Ganjayi MS et al. | β | 2023 | β |
| Sex differences in neuronal activation during aversion-resistant alcohol consumption. | Arnold ME et al. | β | 2023 | β |
| Corticosterone Levels and Glucocorticoid Receptor Gene Expression in High Drinking in the Dark Mice and Their Heterogeneous Stock (HS/NPT) Founder Line. | Savarese AM et al. | β | 2022 | β |
| FACTORS CONTRIBUTING TO THE ESCALATION OF ALCOHOL CONSUMPTION. | Bowen MT et al. | β | 2022 | β |
| Long-term alcohol drinking in High Drinking in the Dark mice is stable for many months and does not show alcohol deprivation effects. | Crabbe JC et al. | β | 2022 | β |
| Midazolam, methamphetamine, morphine and nicotine intake in high-drinking-in-the-dark mice. | Savarese AM et al. | β | 2022 | β |
| Systemic administration of racemic baclofen reduces both acquisition and maintenance of alcohol consumption in male and female mice. | Bauer MR et al. | β | 2022 | β |
| Targeting the Maladaptive Effects of Binge Drinking on Circadian Gene Expression. | Grigsby K et al. | β | 2022 | β |
| Chemogenetic manipulation of astrocytic signaling in the basolateral amygdala reduces binge-like alcohol consumption in male mice. | Nwachukwu KN et al. | β | 2021 | β |
| Ethanol-Related Behaviors in Mouse Lines Selectively Bred for Drinking to Intoxication. | Jensen BE et al. | β | 2021 | β |
| Genotype-dependent epigenetic regulation of DLGAP2 in alcohol use and dependence. | Meng W et al. | β | 2021 | β |
| On the Use of Heterogeneous Stock Mice to Map Transcriptomes Associated With Excessive Ethanol Consumption. | Hitzemann R et al. | β | 2021 | β |
| Recent Perspectives on Sex Differences in Compulsion-Like and Binge Alcohol Drinking. | Radke AK et al. | β | 2021 | β |
| Shortening time for access to alcohol drives up front-loading behavior, bringing consumption in male rats to the level of females. | Flores-Bonilla A et al. | β | 2021 | β |
| Sucrose Consumption Alters Serotonin/Glutamate Co-localisation Within the Prefrontal Cortex and Hippocampus of Mice. | Beecher K et al. | β | 2021 | β |
| The impact of Drinking in the Dark (DID) procedural manipulations on ethanol intake in High Drinking in the Dark (HDID) mice. | Savarese AM et al. | β | 2021 | β |
| The Role of Neuropeptide Y in the Nucleus Accumbens. | Tanaka M et al. | β | 2021 | β |
| Alcohol Binge Drinking and Anxiety-Like Behavior in Socialized Versus Isolated C57BL/6J Mice. | Evans O et al. | β | 2020 | β |
| A prior history of binge-drinking increases sensitivity to the motivational valence of methamphetamine in female C57BL/6J mice. | Sern KR et al. | β | 2020 | β |
| Chronic Chemogenetic Stimulation of the Nucleus Accumbens Produces Lasting Reductions in Binge Drinking and Ameliorates Alcohol-Related Morphological and Transcriptional Changes. | Pozhidayeva DY et al. | β | 2020 | β |
| Chronic Voluntary Binge Ethanol Consumption Causes Sex-Specific Differences in Microglial Signaling Pathways and Withdrawal-associated Behaviors in Mice. | Rath M et al. | β | 2020 | β |
| Combined Effects of Repetitive Mild Traumatic Brain Injury and Alcohol Drinking on the Neuroinflammatory Cytokine Response and Cognitive Behavioral Outcomes. | Hoffman J et al. | β | 2020 | β |
| Effects of Alcohol and Cocaine in a Mutant Mouse Model of Predisposition to Post-Traumatic Stress Disorder. | Paizanis E et al. | β | 2020 | β |
| Effects of Pharmacologically Targeting Neuroimmune Pathways on Alcohol Drinking in Mice Selectively Bred to Drink to Intoxication. | Ozburn AR et al. | β | 2020 | β |
| Effects of Tacrolimus and Other Immune Targeting Compounds on Binge-Like Ethanol Drinking in High Drinking in the Dark Mice. | Grigsby KB et al. | β | 2020 | β |
| High-Intensity Drinking in Adult Australian Twins. | Dash GF et al. | β | 2020 | β |
| Increased Responding for Alcohol and Resistance to Aversion in Female Mice. | Sneddon EA et al. | β | 2020 | β |
| Leveraging Neural Networks in Preclinical Alcohol Research. | Smith LC et al. | β | 2020 | β |
| Sex Differences in the Neurobiology of Alcohol Use Disorder. | Flores-Bonilla A et al. | β | 2020 | β |
| Targeting the Glucocorticoid Receptor Reduces Binge-Like Drinking in High Drinking in the Dark (HDID-1) Mice. | Savarese AM et al. | β | 2020 | β |
| Tetracycline derivatives reduce binge alcohol consumption in High Drinking in the Dark mice. | Crabbe JC et al. | β | 2020 | β |
| A comparison of hippocampal microglial responses in aged and young rodents following dependent and non-dependent binge drinking. | Grifasi IR et al. | β | 2019 | β |
| Animal models of binge drinking, current challenges to improve face validity. | Jeanblanc J et al. | β | 2019 | β |
| Dissecting Brain Networks Underlying Alcohol Binge Drinking Using a Systems Genomics Approach. | Ferguson LB et al. | β | 2019 | β |
| Dynorphin-kappa opioid receptor activity in the central amygdala modulates binge-like alcohol drinking in mice. | Anderson RI et al. | β | 2019 | β |
| Ethanol Conditioned Taste Aversion in High Drinking in the Dark Mice. | Crabbe JC et al. | β | 2019 | β |
| Individual Differences in Ethanol Drinking and Seeking Behaviors in Rats Exposed to Chronic Intermittent Ethanol Vapor Exposure is Associated with Altered CaMKII Autophosphorylation in the Nucleus Accumbens Shell. | Somkuwar SS et al. | β | 2019 | β |
| Sex Differences in Binge-Like and Aversion-Resistant Alcohol Drinking in C57BL/6J Mice. | Sneddon EA et al. | β | 2019 | β |
| Voluntary elevated ethanol consumption in adolescent Sprague-Dawley rats: Procedural contributors and age-specificity. | HosovΓ‘ D et al. | β | 2019 | β |
| Gender-Specific Effects of Selection for Drinking in the Dark on the Network Roles of Coding and Noncoding RNAs. | Iancu OD et al. | β | 2018 | β |
| Genome-Wide Expression Profiles Drive Discovery of Novel Compounds that Reduce Binge Drinking in Mice. | Ferguson LB et al. | β | 2018 | β |
| Investigational drugs for alcohol use disorders: a review of preclinical data. | Ch'Ng SS et al. | β | 2018 | β |
| Alignment of the transcriptome with individual variation in animals selectively bred for High Drinking-In-the-Dark (HDID). | Hitzemann R et al. | β | 2017 | β |
| Environmental Enrichment Blunts Ethanol Consumption after Restraint Stress in C57BL/6 Mice. | Marianno P et al. | β | 2017 | β |
| High Drinking in the Dark (HDID) mice are sensitive to the effects of some clinically relevant drugs to reduce binge-like drinking. | Crabbe JC et al. | β | 2017 | β |
| Negative Affect and Excessive Alcohol Intake Incubate during Protracted Withdrawal from Binge-Drinking in Adolescent, But Not Adult, Mice. | Lee KM et al. | β | 2017 | β |
| Preclinical voluntary drinking models for alcohol abstinence-induced affective disturbances in mice. | Holleran KM et al. | β | 2017 | β |
| Rat animal models for screening medications to treat alcohol use disorders. | Bell RL et al. | β | 2017 | β |
| Critical needs in drug discovery for cessation of alcohol and nicotine polysubstance abuse. | Van Skike CE et al. | β | 2016 | β |
| Effects of Adolescent Intermittent Alcohol Exposure on the Expression of Endocannabinoid Signaling-Related Proteins in the Spleen of Young Adult Rats. | PavΓ³n FJ et al. | β | 2016 | β |
| Fear conditioning in mouse lines genetically selected for binge-like ethanol drinking. | Crabbe JC et al. | β | 2016 | β |
| Nest building is a novel method for indexing severity of alcohol withdrawal in mice. | Greenberg GD et al. | β | 2016 | β |
| Neuropeptide Y response to alcohol is altered in nucleus accumbens of mice selectively bred for drinking to intoxication. | Barkley-Levenson AM et al. | β | 2016 | β |
| Protein Kinase C Epsilon Activity in the Nucleus Accumbens and Central Nucleus of the Amygdala Mediates Binge Alcohol Consumption. | Cozzoli DK et al. | β | 2016 | β |
| Using In Vitro Electrophysiology to Screen Medications: Accumbal Plasticity as an Engram of Alcohol Dependence. | Renteria R et al. | β | 2016 | β |
| Binge alcohol drinking elicits persistent negative affect in mice. | Lee KM et al. | β | 2015 | β |
| Chronobiology of ethanol: animal models. | Rosenwasser AM | β | 2015 | β |
| Distinct ethanol drinking microstructures in two replicate lines of mice selected for drinking to intoxication. | Barkley-Levenson AM et al. | β | 2015 | β |
| Ethanol-induced epigenetic regulations at the Bdnf gene in C57BL/6J mice. | Stragier E et al. | β | 2015 | β |
| Genotypic and sex differences in anxiety-like behavior and alcohol-induced anxiolysis in High Drinking in the Dark selected mice. | Barkley-Levenson AM et al. | β | 2015 | β |
| Individual Variation in Alcohol Intake Predicts Reinforcement, Motivation, and Compulsive Alcohol Use in Rats. | Spoelder M et al. | β | 2015 | β |
| Influence of sex on genetic regulation of "drinking in the dark" alcohol consumption. | Vanderlinden LA et al. | β | 2015 | β |
| Rewarding and aversive effects of ethanol in High Drinking in the Dark selectively bred mice. | Barkley-Levenson AM et al. | β | 2015 | β |
| Alcohol binge drinking during adolescence or dependence during adulthood reduces prefrontal myelin in male rats. | Vargas WM et al. | β | 2014 | β |
| Alcohol, stress hormones, and the prefrontal cortex: a proposed pathway to the dark side of addiction. | Lu YL et al. | β | 2014 | β |
| Behavioral disinhibition in mice bred for high drinking in the dark (HDID) and HS controls increases following ethanol. | Tipps ME et al. | β | 2014 | β |
| Binge alcohol drinking by mice requires intact group 1 metabotropic glutamate receptor signaling within the central nucleus of the amygdala. | Cozzoli DK et al. | β | 2014 | β |
| Circadian rhythms and addiction: mechanistic insights and future directions. | Logan RW et al. | β | 2014 | β |
| "Drinking in the Dark" (DID): a simple mouse model of binge-like alcohol intake. | Thiele TE et al. | β | 2014 | β |
| "Drinking in the dark" (DID) procedures: a model of binge-like ethanol drinking in non-dependent mice. | Thiele TE et al. | β | 2014 | β |
| Genetic relationship between predisposition for binge alcohol consumption and blunted sensitivity to adverse effects of alcohol in mice. | Fritz BM et al. | β | 2014 | β |
| High drinking in the dark mice: a genetic model of drinking to intoxication. | Barkley-Levenson AM et al. | β | 2014 | β |
| Progress in a replicated selection for elevated blood ethanol concentrations in HDID mice. | Crabbe JC et al. | β | 2014 | β |
| Rodent models of genetic contributions to motivation to abuse alcohol. | Crabbe JC | β | 2014 | β |
| Use of animal models of alcohol-related behavior. | Crabbe JC | β | 2014 | β |
| Animal models of alcohol and drug dependence. | Planeta CS | β | 2013 | β |
| Chronic voluntary alcohol consumption results in tolerance to sedative/hypnotic and hypothermic effects of alcohol in hybrid mice. | Ozburn AR et al. | β | 2013 | β |
| Determining the heritability of ethanol-induced locomotor sensitization in mice using short-term behavioral selection. | Linsenbardt DN et al. | β | 2013 | β |
| Escalation of intake under intermittent ethanol access in diverse mouse genotypes. | Rosenwasser AM et al. | β | 2013 | β |
| Ethanol drinking in withdrawal seizure-prone and -resistant selected mouse lines. | Crabbe JC et al. | β | 2013 | β |
| Genetic studies of acute tolerance, rapid tolerance, and drinking in the dark in the LXS recombinant inbred strains. | Radcliffe RA et al. | β | 2013 | β |
| Modeling the diagnostic criteria for alcohol dependence with genetic animal models. | Crabbe JC et al. | β | 2013 | β |
| Pharmacological characterization of the 20% alcohol intermittent access model in Sardinian alcohol-preferring rats: a model of binge-like drinking. | Sabino V et al. | β | 2013 | β |
| Selection for drinking in the dark alters brain gene coexpression networks. | Iancu OD et al. | β | 2013 | β |
| Selective breeding for ethanol-related traits alters circadian phenotype. | McCulley WD et al. | β | 2013 | β |
| Animal models for medications development targeting alcohol abuse using selectively bred rat lines: neurobiological and pharmacological validity. | Bell RL et al. | β | 2012 | β |
| A transcriptional study in mice with different ethanol-drinking profiles: possible involvement of the GABA(B) receptor. | Ribeiro AF et al. | β | 2012 | β |
| Bridging Animal and Human Models: Translating From (and to) Animal Genetics. | Barkley-Levenson AM et al. | β | 2012 | β |
| Ethanol drinking-in-the-dark facilitates behavioral sensitization to ethanol in C57BL/6J, BALB/cByJ, but not in mu-opioid receptor deficient CXBK mice. | TarragΓ³n E et al. | β | 2012 | β |
| Ethanol drinking microstructure of a high drinking in the dark selected mouse line. | Barkley-Levenson AM et al. | β | 2012 | β |
| Ethanol sensitivity in high drinking in the dark selectively bred mice. | Crabbe JC et al. | β | 2012 | β |
| Ethanol tolerance and withdrawal severity in high drinking in the dark selectively bred mice. | Crabbe JC et al. | β | 2012 | β |
| Ethanol up-regulates nucleus accumbens neuronal activity dependent pentraxin (Narp): implications for alcohol-induced behavioral plasticity. | Ary AW et al. | β | 2012 | β |
| Ethanol Withdrawal-Associated Drinking and Drinking in the Dark: Common and Discrete Genetic Contributions. | Crabbe JC et al. | β | 2012 | β |
| GABA(B) receptor agonist only reduces ethanol drinking in light-drinking mice. | Villas Boas GR et al. | β | 2012 | β |
| Intermittent availability of ethanol does not always lead to elevated drinking in mice. | Crabbe JC et al. | β | 2012 | β |
| Nucleus accumbens mGluR5-associated signaling regulates binge alcohol drinking under drinking-in-the-dark procedures. | Cozzoli DK et al. | β | 2012 | β |
| Oral Nicotine Self-Administration in Rodents. | Collins AC et al. | β | 2012 | β |
| The neurobiology of binge-like ethanol drinking: evidence from rodent models. | Sprow GM et al. | β | 2012 | β |
| Translational behaviour-genetic studies of alcohol: are we there yet? | Crabbe JC | β | 2012 | β |
| Alcohol preference drinking in a mouse line selectively bred for high drinking in the dark. | Crabbe JC et al. | β | 2011 | β |
| Derivation and characterization of replicate high- and low-alcohol preferring lines of mice and a high-drinking crossed HAP line. | Oberlin B et al. | β | 2011 | β |
| Ethanol concentration-dependent effects and the role of stress on ethanol drinking in corticotropin-releasing factor type 1 and double type 1 and 2 receptor knockout mice. | Pastor R et al. | β | 2011 | β |
| Intermittent (every-other-day) drinking induces rapid escalation of ethanol intake and preference in adolescent and adult C57BL/6J mice. | Melendez RI | β | 2011 | β |
| Limited access ethanol drinking in the dark in adolescent and adult mice. | Metten P et al. | β | 2011 | β |
| Modeling binge-like ethanol drinking by peri-adolescent and adult P rats. | Bell RL et al. | β | 2011 | β |
| Molecular profiles of drinking alcohol to intoxication in C57BL/6J mice. | Mulligan MK et al. | β | 2011 | β |
| Preclinical studies of alcohol binge drinking. | Crabbe JC et al. | β | 2011 | β |
| The genetic basis of delay discounting and its genetic relationship to alcohol dependence. | Mitchell SH | β | 2011 | β |
| A method for mapping intralocus interactions influencing excessive alcohol drinking. | Phillips TJ et al. | β | 2010 | β |
| Consilience of rodent and human phenotypes relevant for alcohol dependence. | Crabbe JC | β | 2010 | β |
| Consilient research approaches in studying gene x environment interactions in alcohol research. | Sher KJ et al. | β | 2010 | β |
| Ethanol consumption: how should we measure it? Achieving consilience between human and animal phenotypes. | Leeman RF et al. | β | 2010 | β |
| Genetic research: who is at risk for alcoholism. | Foroud T et al. | β | 2010 | β |
| Genetic variation and brain gene expression in rodent models of alcoholism implications for medication development. | BjΓΆrk K et al. | β | 2010 | β |
| Increase in alcohol intake, reduced flexibility of alcohol drinking, and evidence of signs of alcohol intoxication in Sardinian alcohol-preferring rats exposed to intermittent access to 20% alcohol. | Loi B et al. | β | 2010 | β |
| The complexity of alcohol drinking: studies in rodent genetic models. | Crabbe JC et al. | β | 2010 | β |
| Binge drinking upregulates accumbens mGluR5-Homer2-PI3K signaling: functional implications for alcoholism. | Cozzoli DK et al. | β | 2009 | β |
| Review. Neurogenetic studies of alcohol addiction. | Crabbe JC | β | 2008 | β |