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四种不同近交系小鼠青少年和成年期可卡因急性运动反应。

Acute locomotor responses to cocaine in adolescents vs. adults from four divergent inbred mouse strains.

机构信息

Department of Psychology, The Beckman Institute, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

出版信息

Genes Brain Behav. 2010 Nov;9(8):892-8. doi: 10.1111/j.1601-183X.2010.00630.x.

Abstract

Growing evidence suggests that adolescent mice display differential sensitivity to the acute locomotor activating effects of cocaine as compared to adults, but the direction of the difference varies across studies and the reasons are not clear. Few studies have directly examined genetic contributions to age differences in locomotor stimulation from cocaine. The goal of this study was to determine the extent to which reduced stimulation in C57BL/6J adolescents as compared to adults generalizes to other strains. Therefore, we examined male and female mice from four genetically divergent inbred stains (BALB/cByJ, C57BL/6J, DBA/2J and FVB/NJ) at two ages, postnatal day 30 and postnatal day 65. Mice received either saline or cocaine (15 or 30 mg/kg), and then immediately were placed back into their home cages. Locomotor activity was recorded continuously in the home cage by video tracking. Adolescents displayed reduced stimulation as compared to adults for C57BL/6J, BALB/cByJ and female FVB/NJ mice. No age differences were observed for DBA/2J or male FVB/NJ. No main effects of sex were observed. Strain differences in pharmacokinetics, neural development or physiology could contribute to the observed differences between ages across strains. Future comparative studies could discover biological differences between strains that explain age differences in cocaine sensitivity.

摘要

越来越多的证据表明,与成年人相比,青春期小鼠对可卡因的急性运动激活作用表现出不同的敏感性,但这种差异在不同的研究中方向不同,原因尚不清楚。很少有研究直接研究基因对可卡因引起的运动刺激的年龄差异的贡献。本研究的目的是确定与成年小鼠相比,C57BL/6J 青春期小鼠的刺激减少程度是否普遍适用于其他品系。因此,我们在两个年龄(出生后第 30 天和第 65 天)检查了来自四个遗传上不同的近交系(BALB/cByJ、C57BL/6J、DBA/2J 和 FVB/NJ)的雄性和雌性小鼠。小鼠接受生理盐水或可卡因(15 或 30mg/kg),然后立即放回其巢箱。通过视频跟踪在巢箱中连续记录运动活动。与成年小鼠相比,青春期小鼠的 C57BL/6J、BALB/cByJ 和雌性 FVB/NJ 小鼠的刺激减少。未观察到 DBA/2J 或雄性 FVB/NJ 的年龄差异。未观察到性别主效应。药物代谢动力学、神经发育或生理学方面的品系差异可能导致不同品系之间的年龄差异。未来的比较研究可能会发现解释可卡因敏感性年龄差异的品系之间的生物学差异。

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