High Drinking in the Dark (HDID) mice are sensitive to the effects of some clinically relevant drugs to reduce binge-like drinking
暂无分享,去创建一个
J. Crabbe | A. Ozburn | A. Barkley-Levenson | P. Metten | Lawrence C. Huang | J. Schlumbohm | S. Spence | Wyatt R. Hack
[1] S. Hauser,et al. Rat animal models for screening medications to treat alcohol use disorders , 2017, Neuropharmacology.
[2] R. Weinshilboum,et al. Combined Effects of Acamprosate and Escitalopram on Ethanol Consumption in Mice. , 2016, Alcoholism, clinical and experimental research.
[3] S. Boehm,et al. Rodent models and mechanisms of voluntary binge-like ethanol consumption: Examples, opportunities, and strategies for preclinical research , 2016, Progress in Neuro-Psychopharmacology and Biological Psychiatry.
[4] K. Mann,et al. Does Acamprosate Really Produce its Anti-Relapse Effects via Calcium? No Support from the PREDICT Study in Human Alcoholics , 2016, Neuropsychopharmacology.
[5] F. Carvajal,et al. Evidence that Melanocortin Receptor Agonist Melanotan-II Synergistically Augments the Ability of Naltrexone to Blunt Binge-Like Ethanol Intake in Male C57BL/6J Mice. , 2015, Alcoholism, clinical and experimental research.
[6] C. Whittington,et al. The efficacy of acamprosate and naltrexone in the treatment of alcohol dependence, Europe versus the rest of the world: a meta-analysis. , 2015, Addiction.
[7] P. Crowley. Long-term drug treatment of patients with alcohol dependence. , 2015, Australian prescriber.
[8] S. Boehm,et al. Bidirectional enantioselective effects of the GABAB receptor agonist baclofen in two mouse models of excessive ethanol consumption. , 2015, Alcohol.
[9] J. Crabbe,et al. Rewarding and aversive effects of ethanol in High Drinking in the Dark selectively bred mice , 2015, Addiction biology.
[10] P. Borro,et al. Treatment of alcohol dependence: recent progress and reduction of consumption. , 2014, Minerva medica.
[11] A. Heinz,et al. Predicting naltrexone response in alcohol-dependent patients: the contribution of functional magnetic resonance imaging. , 2014, Alcoholism, clinical and experimental research.
[12] S. Boehm,et al. Intra-nucleus accumbens shell injections of R(+)- and S(−)-baclofen bidirectionally alter binge-like ethanol, but not saccharin, intake in C57Bl/6J mice , 2014, Behavioural Brain Research.
[13] G. Bobashev,et al. Clinical and biological moderators of response to naltrexone in alcohol dependence: a systematic review of the evidence. , 2014, Addiction.
[14] J. Crabbe,et al. “Drinking in the Dark” (DID): A Simple Mouse Model of Binge‐Like Alcohol Intake , 2014, Current protocols in neuroscience.
[15] G. Colombo,et al. GABAB receptor ligands for the treatment of alcohol use disorder: preclinical and clinical evidence , 2014, Front. Neurosci..
[16] J. Crabbe,et al. High drinking in the dark mice: a genetic model of drinking to intoxication. , 2014, Alcohol.
[17] R. Spanagel,et al. Acamprosate Produces Its Anti-Relapse Effects Via Calcium , 2014, Neuropsychopharmacology.
[18] J. Crabbe,et al. Progress in a replicated selection for elevated blood ethanol concentrations in HDID mice , 2014, Genes, brain, and behavior.
[19] J. Crabbe. The Genetic Complexity of Alcohol Drinking in Rodents , 2014 .
[20] J. Crabbe,et al. Selection for drinking in the dark alters brain gene coexpression networks. , 2013, Alcoholism, clinical and experimental research.
[21] A. Tomie,et al. Effects of naltrexone on post-abstinence alcohol drinking in C57BL/6NCRL and DBA/2J mice , 2013, Progress in Neuro-Psychopharmacology and Biological Psychiatry.
[22] John P. Didion,et al. Deconstructing Mus gemischus: advances in understanding ancestry, structure, and variation in the genome of the laboratory mouse , 2013, Mammalian Genome.
[23] M. Olive,et al. Safety and Efficacy of Acamprosate for the Treatment of Alcohol Dependence , 2013, Substance abuse : research and treatment.
[24] L. Lumeng,et al. Animal models for medications development targeting alcohol abuse using selectively bred rat lines: Neurobiological and pharmacological validity , 2012, Pharmacology Biochemistry and Behavior.
[25] J. Crabbe,et al. Ethanol Withdrawal-Associated Drinking and Drinking in the Dark: Common and Discrete Genetic Contributions , 2012, Addiction genetics.
[26] P. Kalivas,et al. Glutamatergic medications for the treatment of drug and behavioral addictions , 2012, Pharmacology Biochemistry and Behavior.
[27] D. Goldman,et al. Pharmacogenetic approaches to the treatment of alcohol addiction , 2011, Nature Reviews Neuroscience.
[28] R. Prosser,et al. Circadian and Acamprosate Modulation of Elevated Ethanol Drinking in mPer2 Clock Gene Mutant Mice , 2011, Chronobiology international.
[29] J. Crabbe,et al. Alcohol preference drinking in a mouse line selectively bred for high drinking in the dark. , 2011, Alcohol.
[30] R. Prosser,et al. Acamprosate-responsive brain sites for suppression of ethanol intake and preference. , 2011, American journal of physiology. Regulatory, integrative and comparative physiology.
[31] N. Grahame,et al. Derivation and Characterization of Replicate High- and Low-Alcohol Preferring Lines of Mice and a High-Drinking Crossed HAP Line , 2011, Behavior genetics.
[32] M. Ford,et al. Assessment of GABA-B, metabotropic glutamate, and opioid receptor involvement in an animal model of binge drinking. , 2011, Alcohol.
[33] G. Koob,et al. Preclinical studies of alcohol binge drinking , 2011, Annals of the New York Academy of Sciences.
[34] D. Hommer,et al. Translating the neuroscience of alcoholism into clinical treatments: From blocking the buzz to curing the blues , 2010, Neuroscience & Biobehavioral Reviews.
[35] K. Mann,et al. Acamprosate: how, where, and for whom does it work? Mechanism of action, treatment targets, and individualized therapy. , 2010, Current pharmaceutical design.
[36] J. Crabbe,et al. A Line of Mice Selected for High Blood Ethanol Concentrations Shows Drinking in the Dark to Intoxication , 2009, Biological Psychiatry.
[37] D. Linsenbardt,et al. GABAergic modulation of binge-like ethanol intake in C57BL/6J mice , 2007, Pharmacology Biochemistry and Behavior.
[38] J. Crabbe,et al. Increased drinking during withdrawal from intermittent ethanol exposure is blocked by the CRF receptor antagonist D-Phe-CRF(12-41). , 2007, Alcoholism, clinical and experimental research.
[39] J. Rhodes,et al. Acute effects of Naltrexone and GBR 12909 on ethanol drinking-in-the-dark in C57BL/6J mice , 2007, Psychopharmacology.
[40] J. Crabbe,et al. Stability of inbred mouse strain differences in behavior and brain size between laboratories and across decades , 2006, Proceedings of the National Academy of Sciences.
[41] M. Egli. Can experimental paradigms and animal models be used to discover clinically effective medications for alcoholism? , 2005, Addiction biology.
[42] A. Sharpe,et al. Ataxia and c-Fos expression in mice drinking ethanol in a limited access session. , 2005, Alcoholism, clinical and experimental research.
[43] J. Crabbe,et al. A procedure to produce high alcohol intake in mice , 2005, Psychopharmacology.
[44] J. Crabbe,et al. Evaluation of a simple model of ethanol drinking to intoxication in C57BL/6J mice , 2005, Physiology & Behavior.
[45] J. Crabbe,et al. Genetic Analysis of Rapid Tolerance to Ethanol's Incoordinating Effects in Mice: Inbred Strains and Artificial Selection , 2004, Behavior genetics.
[46] J. Park,et al. Effect of the combination of naltrexone and acamprosate on alcohol intake in mice , 2004, Psychiatry and clinical neurosciences.
[47] W. Zieglgänsberger,et al. Pharmacological mechanisms of naltrexone and acamprosate in the prevention of relapse in alcohol dependence. , 2003, The American journal on addictions.
[48] C. Hodge,et al. Effects of acute acamprosate and homotaurine on ethanol intake and ethanol-stimulated mesolimbic dopamine release. , 2002, European journal of pharmacology.
[49] L. Toth,et al. Food and water restriction protocols: physiological and behavioral considerations. , 2000, Contemporary topics in laboratory animal science.
[50] R. Spanagel,et al. Acamprosate and alcohol: I. Effects on alcohol intake following alcohol deprivation in the rat. , 1996, European journal of pharmacology.
[51] J. Crabbe,et al. Estimation of genetic correlation: interpretation of experiments using selectively bred and inbred animals. , 1990, Alcoholism, clinical and experimental research.
[52] H. Grüneberg,et al. Introduction to quantitative genetics , 1960 .
[53] J. Crabbe. Use of animal models of alcohol-related behavior. , 2014, Handbook of clinical neurology.
[54] Gunter Schumann,et al. The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption , 2005, Nature Medicine.