Animal models that explore differential sensitivity to the effects of acute and  repeated exposure of alcohol (ethanol) may be influenced by both the  developmental and genetic profile of the population. 
Therefore, we sought to compare the influence of ontogeny on sensitivity to ethanol-induced locomotor stimulation and on the induction of locomotor sensitization to this effect across 2 inbred strains of mice; the ethanol consuming C57BL/6J and the ethanol avoiding DBA/2J strains.
Therefore, we sought to compare the influence of ontogeny on sensitivity to ethanol-induced locomotor stimulation and on the induction of locomotor sensitization to this effect across 2 inbred strains of mice; the ethanol consuming C57BL/6J and the ethanol avoiding DBA/2J strains.
 C57BL/6J and DBA/2J adults (postnatal day [PD] 60 to 80) and  adolescents (PD 30 ± 2) were assessed for basal activity, acute response to  2.0 g/kg ethanol, and the expression of locomotor sensitization following  repeated administration of 2.5, 3.0, or 3.5 g/kg ethanol.
 Basal activity was different across development for the  C57BL/6J, but not DBA/2J, with adult B6 mice showing persistently greater  baseline activity. Adolescents of both strains were more sensitive than adults  to acute ethanol-induced locomotor stimulation; adults exhibited a decrease in  their acute response across the testing session. Adolescent DBA/2J mice  developed less ethanol sensitization compared to adults, with significant  sensitization observed only following repeated administration of the lowest  ethanol dose (2.5 g/kg), whereas DBA/2J adults sensitized to all doses. Age did  not influence the development of ethanol sensitization for the C57BL/6J strain,  as both adults and adolescents displayed a sensitized response following all  ethanol doses.
 These results suggest that the developmental pattern of  locomotor sensitivity to ethanol is unique to the genotypic profile of the  animal model.
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Request Reprint E-Mail: cmelon@iupui.edu
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Request Reprint E-Mail: cmelon@iupui.edu
