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2
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J Psychopharmacol. 2010 Sep;24(9):1411-7. doi: 10.1177/0269881109106976. Epub 2009 Nov 25.
3
Neurobehavioral effects of environmental enrichment and drug abuse vulnerability.环境富集与药物滥用易感性的神经行为效应
Pharmacol Biochem Behav. 2009 May;92(3):377-82. doi: 10.1016/j.pbb.2009.01.016. Epub 2009 Jan 31.
4
Principles of laboratory assessment of drug abuse liability and implications for clinical development.药物滥用倾向的实验室评估原则及其对临床开发的影响。
Drug Alcohol Depend. 2009 Dec 1;105 Suppl 1:S14-25. doi: 10.1016/j.drugalcdep.2009.04.003. Epub 2009 May 14.
5
Different affective response to opioid withdrawal in adolescent and adult mice.青少年和成年小鼠对阿片类药物戒断的不同情感反应。
Life Sci. 2009 Jan 2;84(1-2):52-60. doi: 10.1016/j.lfs.2008.11.002. Epub 2008 Nov 12.
6
Early-onset drug use and risk for drug dependence problems.早期药物使用与药物依赖问题风险
Addict Behav. 2009 Mar;34(3):319-22. doi: 10.1016/j.addbeh.2008.10.021. Epub 2008 Nov 1.
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Increased elevated plus maze open-arm time in mice during spontaneous morphine withdrawal.小鼠在自发吗啡戒断期间高架十字迷宫开放臂停留时间增加。
Behav Brain Res. 2009 Feb 11;197(2):454-6. doi: 10.1016/j.bbr.2008.09.035. Epub 2008 Oct 8.

社会因素对青春期雌性吗啡敏化的影响。

Social influences on morphine sensitization in adolescent females.

机构信息

Behavioral and Cellular Neuroscience, Department of Psychology, Texas A&M University, College Station, TX 77843, USA.

出版信息

Drug Alcohol Depend. 2010 Aug 1;110(3):263-6. doi: 10.1016/j.drugalcdep.2010.03.009. Epub 2010 Apr 24.

DOI:10.1016/j.drugalcdep.2010.03.009
PMID:20456874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2946073/
Abstract

We recently observed that social interactions influence morphine responsiveness in adolescent males. Given sex-related differences in both social interactions and responses to morphine, the present study examines social influences on morphine sensitization in adolescent female mice. Four experimental groups were examined: (1) morphine-treated mice (twice daily, 10-40 mg/kg, s.c.) housed physically and visually separated from saline-treated mice ('morphine only'), (2) morphine-treated mice housed together with saline-treated mice ('morphine cage-mates (of saline)'), (3) saline-treated mice housed together with morphine-treated mice ('saline cage-mates (of morphine)'), and (4) saline-treated mice housed physically and visually separated from morphine-treated mice ('saline only'). Following the treatment period, mice were tested individually for their locomotor response to 20 mg/kg morphine (s.c.). There were no significant differences in morphine-induced hyper-locomotion between saline only and saline cage-mates (of morphine) female adolescent mice. Notably, morphine only mice exhibited significantly greater morphine sensitization as compared to morphine cage-mates (of saline). Thus, this study demonstrates social influences on morphine sensitization in adolescent females. Drug use during early adolescence is a key predictor of later drug abuse and dependence during adulthood. Thus, understanding the specific vulnerabilities to drug use in this age group may represent a first step in helping develop more effective treatment programs.

摘要

我们最近观察到,社交互动会影响青少年男性对吗啡的反应。鉴于社交互动和对吗啡的反应在性别上存在差异,本研究探讨了社交互动对青春期雌性小鼠吗啡敏化的影响。研究考察了四个实验组:(1)吗啡处理的小鼠(每天两次,10-40mg/kg,皮下注射)与生理盐水处理的小鼠在身体和视觉上分开饲养(“仅吗啡”),(2)与生理盐水处理的小鼠一起饲养的吗啡处理的小鼠(“吗啡笼伴(生理盐水)”),(3)与吗啡处理的小鼠一起饲养的生理盐水处理的小鼠(“吗啡笼伴(吗啡)”),以及(4)与吗啡处理的小鼠在身体和视觉上分开饲养的生理盐水处理的小鼠(“仅生理盐水”)。治疗期结束后,对小鼠进行 20mg/kg 吗啡(皮下注射)的单独运动反应测试。仅生理盐水和吗啡笼伴(生理盐水)的雌性未成年小鼠的吗啡诱导过度活跃无显著差异。值得注意的是,仅吗啡的小鼠表现出与吗啡笼伴(吗啡)相比明显更大的吗啡敏化。因此,本研究证明了社交互动对青春期雌性小鼠吗啡敏化的影响。青少年时期的药物使用是成年后药物滥用和依赖的关键预测因素。因此,了解这一年龄组对药物使用的具体脆弱性可能是制定更有效的治疗计划的第一步。