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129X1/SvJ小鼠中可卡因觅求行为的恢复:可卡因激发、可卡因线索及食物剥夺的影响

Reinstatement of cocaine seeking in 129X1/SvJ mice: effects of cocaine priming, cocaine cues and food deprivation.

作者信息

Highfield David A, Mead Andy N, Grimm Jeffrey W, Rocha Beatriz A, Shaham Yavin

机构信息

Behavioral Neuroscience Branch, IRP/NIDA/NIH, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA.

出版信息

Psychopharmacology (Berl). 2002 Jun;161(4):417-24. doi: 10.1007/s00213-002-1047-9. Epub 2002 Apr 24.

Abstract

RATIONALE AND OBJECTIVES

The mechanisms underlying relapse to cocaine seeking induced by exposure to priming cocaine injections, cues associated with cocaine self-administration and environmental stressors have been studied in rats. Here we describe a reinstatement method for studying relapse to cocaine seeking in mice, a suitable species for studying the effect of genetic manipulations such as gene knockout or gene over-expression on compulsive drug use.

METHODS

Male mice of the 129X1/SvJ strain were trained for 14-16 days to self-administer cocaine (0.75 mg/kg/infusion; 4 h/day; fixed-ratio-1 schedule of reinforcement; infusions were paired with a light-tone compound cue). Next, the lever-pressing behavior was extinguished by removing the cocaine syringes in the presence (Exps. 1 and 3) or absence (Exp. 2) of the cocaine cue. Subsequently, tests for reinstatement were conducted after exposure to priming injections of cocaine (0, 1.5, 3.0 and 6.0 mg/kg, IV; Exp. 1), response-contingent presentations of the cocaine-associated cue (Exp. 2), or food deprivation stress (1 and 22 h; Exp. 3).

RESULTS

The effect of cocaine priming on reinstatement was modest and was only observed at the highest dose tested. On the other hand, reinstatement of cocaine seeking was observed following exposure to the cocaine-associated cue and food deprivation stress.

CONCLUSIONS

The present data suggest that factors contributing to relapse to drugs can be studied in the reinstatement model using the common 129X1/SvJ mouse inbred strain.

摘要

原理与目的

在大鼠中,已经对由接触引发性可卡因注射、与可卡因自我给药相关的线索以及环境应激源所诱导的可卡因觅求复发的潜在机制进行了研究。在此,我们描述一种用于研究小鼠可卡因觅求复发的复吸方法,小鼠是研究基因敲除或基因过表达等基因操作对强迫性药物使用影响的合适物种。

方法

对129X1/SvJ品系的雄性小鼠进行14 - 16天的训练,使其自我给药可卡因(0.75毫克/千克/输注;每天4小时;固定比率1强化程序;输注与轻音复合线索配对)。接下来,在存在(实验1和3)或不存在(实验2)可卡因线索的情况下,通过移除可卡因注射器来消除杠杆按压行为。随后,在接触引发性可卡因注射(0、1.5、3.0和6.0毫克/千克,静脉注射;实验1)、可卡因相关线索的反应性呈现(实验2)或食物剥夺应激(1和22小时;实验3)后进行复吸测试。

结果

可卡因引发对复吸的影响较小,仅在测试的最高剂量下观察到。另一方面,在接触可卡因相关线索和食物剥夺应激后观察到可卡因觅求的复吸。

结论

目前的数据表明,使用常见的129X1/SvJ近交系小鼠,可在复吸模型中研究导致药物复发的因素。

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