Literature DB >> 8949958

Self-administration of ethanol: towards the location of predisposing polygenes in quasi-congenic animal models.

C Vadász1, A Fleischer, J LaFrancois, R F Mao.   

Abstract

Alcohol consumption by C57BL/6By background and BALB/cJ donor strains, and by two recently developed quasi-congenic QTL-introgression strains, which share about 96% of their genes with the background strain, was studied in a limited access paradigm. Alcohol and water were offered for 60 min per day using modified pipettes on a drinking cage. Increasing concentration of alcohol solutions, 3, 6, and 12%, were given for days 1-7, 8-14, and 15-22, respectively. Consumption of the 12% alcohol solution was highest in C57BL/6By (0.72 g/kg/h), lowest in BALB/cJ (0.14 g/kg/h). The B6.Cb4i5 beta 13 quasi-congenic strain, in spite of its genetic similarity to the C57BL/6By background strain, consumed significantly less alcohol (0.41 g/kg/h) than the background strain. The results suggest that polygenes that reduce alcohol consumption were introgressed from the BALB/cJ donor strain into the C57BL/6By background strain, and that the b4i5 series of the B6.C quasi-congenic QTL-introgression strains may be useful in mapping genes that influence alcohol-related behaviors. Locations of the introgressed candidate polygenes were tentatively identified by analyzing microsatellite maps of two of the quasi-congenic strains.

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Year:  1996        PMID: 8949958     DOI: 10.1016/s0741-8329(96)00082-1

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  4 in total

1.  Mapping of QTLs for oral alcohol self-administration in B6.C and B6.I quasi-congenic RQI strains.

Authors:  Csaba Vadasz; Mariko Saito; Beatrix M Gyetvai; Melinda Oros; Istvan Szakall; Krisztina M Kovacs; Vidudala V T S Prasad; Grant Morahan; Reka Toth
Journal:  Neurochem Res       Date:  2007-02-02       Impact factor: 3.996

2.  In vivo Proton NMR spectroscopy of genetic mouse models BALB/cJ and C57BL/6By: variation in hippocampal glutamate level and the metabotropic glutamate receptor, subtype 7 (Grm7) gene.

Authors:  David N Guilfoyle; Scott Gerum; Csaba Vadasz
Journal:  J Mol Neurosci       Date:  2014-01-05       Impact factor: 3.444

3.  Selective reduction of cerebral cortex GABA neurons in a late gestation model of fetal alcohol spectrum disorder.

Authors:  John F Smiley; Mariko Saito; Cynthia Bleiwas; Kurt Masiello; Babak Ardekani; David N Guilfoyle; Scott Gerum; Donald A Wilson; Csaba Vadasz
Journal:  Alcohol       Date:  2015-07-21       Impact factor: 2.405

4.  Mesencephalic dopamine neuron number and tyrosine hydroxylase content: Genetic control and candidate genes.

Authors:  C Vadasz; J F Smiley; K Figarsky; M Saito; R Toth; B M Gyetvai; M Oros; K K Kovacs; P Mohan; R Wang
Journal:  Neuroscience       Date:  2007-07-17       Impact factor: 3.590

  4 in total

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