Chronic intermittent toluene inhalation initiated during adolescence in rats does not alter voluntary consumption of ethanol in adulthood

被引:5
|
作者
Dick, Alec L. W. [1 ,2 ]
Lawrence, Andrew J. [1 ,2 ]
Duncan, Jhodie R. [1 ,3 ]
机构
[1] Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[2] Florey Dept Neurosci & Mental Hlth, Heidelberg, Vic, Australia
[3] Univ Melbourne, Dept Anat & Neurosci, Parkville, Vic 3010, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
Inhalant abuse; 2-Bottle choice; Alcohol; Liver; NICOTINIC ACETYLCHOLINE-RECEPTORS; CROSS-SENSITIZATION; LOCOMOTOR-ACTIVITY; NUCLEUS-ACCUMBENS; ABUSED SOLVENT; TIME-COURSE; EXPOSURE; ACCESS; MISUSE; AMPHETAMINE;
D O I
10.1016/j.alcohol.2014.08.001
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Voluntary inhalation of organic solvents, such as toluene, is particularly prevalent in adolescent populations and is considered to be a contributing factor to substance use and dependence later in life. While inhalants are often the initial "drug" experienced during this period, alcohol is another substance readily abused by adolescent populations. Although both substances are thought to have similar actions within the brain, our understanding of the implications of adolescent inhalant abuse upon subsequent exposure to alcohol remains to be investigated. Thus, this study aimed to assess locomotor responses to acute ethanol and voluntary ethanol consumption following a period of toluene inhalation throughout adolescence/early adulthood. Adolescent male Wistar rats (postnatal day [PN] 27) inhaled air or toluene (3000 ppm) for I h/day, 3 days/week for 4 (PN 27-52) or 8 weeks (PN 27-80) to mimic the patterns observed in human inhalant abusers. Following the exposure period, cross-sensitization to acute ethanol challenge (0.5 g/kg, intraperitoneally [i.p.]), and voluntary consumption of 20% ethanol in a chronic intermittent 2-bottle choice paradigm, were assessed. Hepatic ethanol and acetaldehyde metabolism and liver histopathology were also investigated. Chronic intermittent toluene (CIT) exposure throughout adolescence for up to 8 weeks did not alter the behavioral response to acute ethanol or voluntary consumption of ethanol in adulthood, although an age-dependent effect on ethanol consumption was observed (p < 0.05). Both liver function and pathology did not differ between treatment groups. Thus, in the paradigm employed, CIT exposure throughout adolescence and early adulthood did not predispose rats to subsequent locomotor sensitivity or voluntary consumption of ethanol in adulthood. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:561 / 569
页数:9
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