Motor impairment: a new ethanol withdrawal phenotype in mice

Alcoholism is a complex disorder with genetic and environmental risk factors. The presence of withdrawal symptoms is one criterion for alcohol dependence. Genetic animal models have followed a reductionist approach by quantifying various effects of ethanol withdrawal separately. Different ethanol withdrawal symptoms may have distinct genetic etiologies, and therefore differentiating distinct neurobiological mechanisms related to separate signs of withdrawal would increase our understanding of various aspects of the complex phenotype. This study establishes motor incoordination as a new phenotype of alcohol withdrawal in mice. Mice were made physically dependent on ethanol by exposure to ethanol vapor for 72 h. The effects of ethanol withdrawal in mice from different genetic backgrounds were measured on the accelerating rotarod, a simple motor task. Ethanol withdrawal disrupted accelerating rotarod behavior in mice. The disruptive effects of withdrawal suggest a performance rather than a learning deficit. Inbred strain comparisons suggest genetic differences in magnitude of this withdrawal phenotype. The withdrawal-induced deficits were not correlated with the selection response difference in handling convulsion severity in selectively bred Withdrawal Seizure-Prone and Withdrawal Seizure-Resistant lines. The accelerating rotarod seems to be a simple behavioral measure of ethanol withdrawal that is suitable for comparing genotypes.

[1]  S. Qian,et al.  Exploratory activity, motor coordination, and spatial learning in Mchr1 knockout mice , 2007, Behavioural Brain Research.

[2]  S. Al-Rejaie,et al.  Possible role of mouse cerebellar nitric oxide in the behavioral interaction between chronic intracerebellar nicotine and acute ethanol administration: Observation of cross-tolerance , 2006, Neuroscience.

[3]  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.

[4]  S. Al-Rejaie,et al.  Behavioral interaction between nicotine and ethanol: possible modulation by mouse cerebellar glutamate. , 2006, Alcoholism, clinical and experimental research.

[5]  S. Al-Rejaie,et al.  Antagonism of ethanol ataxia by intracerebellar nicotine: Possible modulation by mouse cerebellar nitric oxide and cGMP , 2006, Brain Research Bulletin.

[6]  J. Crabbe,et al.  Alcohol withdrawal severity in inbred mouse (Mus musculus) strains. , 2005, Behavioral neuroscience.

[7]  Robert Lalonde,et al.  Exploratory activity and motor coordination in wild-type SOD1/SOD1 transgenic mice , 2005, Brain Research Bulletin.

[8]  J. Crabbe,et al.  An analysis of the genetics of alcohol intoxication in inbred mice , 2005, Neuroscience & Biobehavioral Reviews.

[9]  C. L. Kliethermes Anxiety-like behaviors following chronic ethanol exposure , 2005, Neuroscience & Biobehavioral Reviews.

[10]  G. Koob,et al.  Allostasis and dysregulation of corticotropin-releasing factor and neuropeptide Y systems: implications for the development of alcoholism , 2004, Pharmacology Biochemistry and Behavior.

[11]  J. Crabbe,et al.  Genetic Analysis of Rapid Tolerance to Ethanol's Incoordinating Effects in Mice: Inbred Strains and Artificial Selection , 2004, Behavior genetics.

[12]  J. Crabbe,et al.  Strain differences in three measures of ethanol intoxication in mice: the screen, dowel and grip strength tests , 2003, Genes, brain, and behavior.

[13]  R. Harris,et al.  Deletion of the fyn-kinase gene alters behavioral sensitivity to ethanol. , 2003, Alcoholism, clinical and experimental research.

[14]  J. Crabbe,et al.  Assessment of genetic susceptibility to ethanol intoxication in mice , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Crabbe Alcohol and genetics: new models. , 2002, American journal of medical genetics.

[16]  M. Dar Mouse cerebellar adenosine-glutamate interactions and modulation of ethanol-induced motor incoordination. , 2002, Alcoholism, clinical and experimental research.

[17]  J. Crabbe,et al.  Sensitivity and tolerance to ethanol-induced incoordination and hypothermia in HAFT and LAFT mice , 2001, Pharmacology Biochemistry and Behavior.

[18]  Janan T. Eppig,et al.  A mouse phenome project , 2000, Mammalian Genome.

[19]  Maja Bucan,et al.  Behavior and mutagenesis screens: the importance of baseline analysis of inbred strains , 2000, Mammalian Genome.

[20]  J. Crabbe,et al.  Sensitivity to ethanol-induced motor incoordination in 5-HT(1B) receptor null mutant mice is task-dependent: implications for behavioral assessment of genetically altered mice. , 2000, Behavioral neuroscience.

[21]  J. Crabbe,et al.  Genetic Determinants of Severity of Acute Withdrawal From Diazepam in Mice Commonality With Ethanol and Pentobarbital , 1999, Pharmacology Biochemistry and Behavior.

[22]  G. Mcclearn,et al.  High genetic susceptibility to ethanol withdrawal predicts low ethanol consumption , 1998, Mammalian Genome.

[23]  E. Saiff Pharmacological Effects of Ethanol on the Nervous System , 1997 .

[24]  M. Dar Mouse cerebellar adenosinergic modulation of ethanol-induced motor incoordination: possible involvement of cAMP , 1997, Brain Research.

[25]  J. Crabbe,et al.  Sensitivity to ethanol-induced ataxia in HOT and COLD selected lines of mice. , 1996, Alcoholism, clinical and experimental research.

[26]  J. Crabbe,et al.  Time course and genetic variation in the regulation of calcium channel antagonist binding sites in rodent tissues during the induction of ethanol physical dependence and withdrawal. , 1995, Alcohol and alcoholism.

[27]  R. Nicoll,et al.  Release of adenosine by activation of NMDA receptors in the hippocampus. , 1994, Science.

[28]  J. Crabbe,et al.  Common genetic determinants of severity of acute withdrawal from ethanol, pentobarbital and diazepam in inbred mice. , 1994, Behavioural pharmacology.

[29]  J. Crabbe,et al.  Indexing withdrawal in mice: matching genotypes for exposure in studies using ethanol vapor inhalation. , 1994, Alcoholism, clinical and experimental research.

[30]  E. Bowman,et al.  Intracerebellar nicotinic-cholinergic participation in the cerebellar adenosinergic modulation of ethanol-induced motor incoordination in mice , 1994, Brain Research.

[31]  J. Crabbe,et al.  Genetic determinants of sensitivity to ethanol in inbred mice. , 1994, Behavioral neuroscience.

[32]  E. Bowman,et al.  Central behavioral interactions between ethanol, (−)-nicotine, and (−)-cotinine in mice , 1993, Brain Research Bulletin.

[33]  J. Crabbe,et al.  Selective breeding for alcohol withdrawal severity , 1993, Behavior genetics.

[34]  J. Crabbe,et al.  Acute dependence on depressant drugs is determined by common genes in mice. , 1991, The Journal of pharmacology and experimental therapeutics.

[35]  J. Crabbe,et al.  Estimation of genetic correlation: interpretation of experiments using selectively bred and inbred animals. , 1990, Alcoholism, clinical and experimental research.

[36]  J. Crabbe,et al.  Selected mouse lines, alcohol and behavior , 1989, Experientia.

[37]  J. Crabbe,et al.  Ethanol withdrawal in mice bred to be genetically prone or resistant to ethanol withdrawal seizures. , 1986, The Journal of pharmacology and experimental therapeutics.

[38]  J. Crabbe,et al.  Bidirectional selection for susceptibility to ethanol withdrawal seizures inMus musculus , 1985, Behavior genetics.

[39]  V. Bogo,et al.  Comparison of accelerod and rotarod sensitivity in detecting ethanol- and acrylamide-induced performance decrement in rats: review of experimental considerations of rotating rod systems. , 1981, Neurotoxicology.

[40]  D. B. Goldstein Inherited Differences in Intensity of Alcohol Withdrawal Reactions in Mice , 1973, Nature.

[41]  D. B. Goldstein Relationship of alcohol dose to intensity of withdrawal signs in mice. , 1972, The Journal of pharmacology and experimental therapeutics.

[42]  D. B. Goldstein,et al.  Alcohol Dependence Produced in Mice by Inhalation of Ethanol: Grading the Withdrawal Reaction , 1971, Science.

[43]  D. Roberts,et al.  The quantitative measurement of motor inco‐ordination in naive mice using an accelerating rotarod , 1968 .

[44]  N W DUNHAM,et al.  A note on a simple apparatus for detecting neurological deficit in rats and mice. , 1957, Journal of the American Pharmaceutical Association. American Pharmaceutical Association.

[45]  Kenneth J Sher,et al.  The development of alcohol use disorders. , 2005, Annual review of clinical psychology.

[46]  H. Barry,et al.  Drug effects on motor coordination , 2004, Psychopharmacologia.

[47]  D. Roberts,et al.  A rotarod suitable for quantitative measurements of motor incoordination in naive mice , 2004, Naunyn-Schmiedebergs Archiv für Pharmakologie und experimentelle Pathologie.

[48]  Douglas Wahlsten,et al.  Different data from different labs: lessons from studies of gene-environment interaction. , 2003, Journal of neurobiology.

[49]  J. Crabbe Genetic contributions to addiction. , 2002, Annual review of psychology.

[50]  J. Crabbe,et al.  Alcohol dependence and withdrawal: a genetic animal model. , 1990, Annals of medicine.

[51]  D. Roberts,et al.  The quantiative measurement of motor inco-ordination in naive mice using an acelerating rotarod. , 1968, The Journal of pharmacy and pharmacology.