首页> 外文期刊>Psychopharmacology >Assessment of the aversive and rewarding effects of alcohol in Fischer and Lewis rats.
【24h】

Assessment of the aversive and rewarding effects of alcohol in Fischer and Lewis rats.

机译:评估酒精对费舍尔和刘易斯大鼠的厌恶和奖励作用。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

RATIONALE: Application of the Fischer-Lewis genetic model of drug abuse to the study of alcohol's motivational properties has been limited. OBJECTIVES: To assess the aversive and rewarding effects of ethanol in Fischer and Lewis rats. MATERIALS AND METHODS: Fischer and Lewis rats underwent a four-trial combined conditioned taste aversion/conditioned place preference procedure (CTA/CPP; 0, 1, 1.25, or 1.5 g/kg IP ethanol). Others received 0, 1, or 1.5 g/kg followed by tail blood sampling at 15-, 60- and 180-min post-injection. In additional groups, hypothermia to 0, 1.5, and 3 g/kg was assessed before and 30- and 60-min post-injection. RESULTS: All alcohol-treated groups except low-dose Lewis acquired CTA after one trial. Fischer rats developed stronger CTAs than Lewis at 1.25 and 1.5 g/kg. Ethanol-induced reward in taste or place conditioning was not evident in either strain. Lewis animals showed overall higher peak blood alcohol concentrations, but hypothermia did not vary by strain. CONCLUSION: Compared to Fischer, Lewis rats are less sensitive to alcohol's aversive effects as assessed in the CTA paradigm. The behavioral differences observed are not due to hypothermia, but pharmacokinetic differences may contribute. These data underscore the importance of genetic factors and the aversive effects of initial drug exposures in modeling vulnerability to abuse. In addition to its application with other drugs, the Fischer-Lewis model may be useful for investigating the biobehavioral bases of alcohol abuse.
机译:理由:滥用药物的费歇尔-刘易斯遗传模型在研究酒精动机特性方面的应用受到限制。目的:评估乙醇对费希尔和刘易斯大鼠的厌恶和奖励作用。材料与方法:Fischer和Lewis大鼠进行了四次组合式条件厌恶/条件位置偏爱程序(CTA / CPP; 0、1、1.25或1.5 g / kg IP乙醇)。其他人接受0、1或1.5 g / kg,然后在注射后15分钟,60分钟和180分钟进行尾血采样。在另外的组中,在注射前以及注射后30分钟和60分钟评估低温至0、1.5和3 g / kg。结果:除低剂量刘易斯外,所有酒精治疗组均在一项试验后获得了CTA。 Fischer大鼠在1.25和1.5 g / kg时比Lewis产生更强的CTAs。在这两种菌株中,乙醇诱导的味道或位置调节奖励均不明显。刘易斯动物总体上显示出较高的峰值血液酒精浓度,但体温过低不会因品系而异。结论:与Fischer相比,Lewis大鼠对酒精的厌恶作用不那么敏感,如CTA范例所评估。观察到的行为差异不是由于体温过低引起的,而是可能导致药代动力学差异。这些数据强调了遗传因素的重要性以及初始药物暴露对建模滥用行为的厌恶作用。 Fischer-Lewis模型除了与其他药物一起使用外,还可用于研究酗酒的生物行为基础。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号