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在恐惧增强惊吓试验(一种用于探究与药物相关动机状态的跨学科测试)中观察到阿片类药物戒断的类焦虑效应。

Anxiogenic-like effects of opiate withdrawal seen in the fear-potentiated startle test, an interdisciplinary probe for drug-related motivational states.

作者信息

Fendt M, Mucha R F

机构信息

Tierphysiologie, Universität Tübingen, Germany.

出版信息

Psychopharmacology (Berl). 2001 May;155(3):242-50. doi: 10.1007/s002130100709.

Abstract

RATIONALE

Anxiety-like effects may be universal to withdrawal from drugs of abuse. The study of withdrawal would benefit from the acoustic startle response (ASR), a discrete, cross-species reflex which is increased by fear-related states. However, existing reports of opiate-related effects on baseline ASR have not validated ASR as a measure of drug-related motivation.

OBJECTIVE

The effects of opiate treatment and withdrawal were examined using fear-potentiated startle, a startle test more sensitive to fear than baseline changes.

METHODS

Fear-conditioned rats were treated with Alzet osmotic pumps delivering 0.25 mg/kg per day fentanyl or placebo pumps. Experiment I examined changes before and during opiate treatment on locomotor activity and baseline, prepulse inhibition, and fear-potentiated startle. Experiment 2 examined the same responses during withdrawal precipitated after 4-7 days of treatment using IV naloxone.

RESULTS

Experiment 1 revealed an attenuated fear-potentiated startle on the first test after the start of fentanyl treatment (4 h); this was not seen on subsequent tests and suggested tolerance to this acute effect. Experiment 2 found an enhancement of fear-potentiated startle precipitated in fentanyl-treated rats after injection of 0.025 and 0.16 mg/kg naloxone; this was not seen at 1 mg/kg naloxone, even though more physical withdrawal signs were most prevalent at this dose. In neither experiment did locomotor activity, baseline ASR, or prepulse inhibition of the ASR show any treatment effect.

CONCLUSIONS

Fear-potentiated startle may provide a specific and valid measure of anxiety-like effects of drug withdrawal. Discussed were conditions needed to see this effect and the relevance of the findings for different mechanisms of withdrawal discomfort.

摘要

原理

戒断滥用药物可能普遍会产生类似焦虑的效应。对戒断反应的研究可借助听觉惊吓反应(ASR),这是一种离散的、跨物种的反射,会因恐惧相关状态而增强。然而,现有关于阿片类药物对基线ASR影响的报告尚未验证ASR可作为药物相关动机的一种衡量指标。

目的

使用恐惧增强惊吓反应来研究阿片类药物治疗及戒断的效应,该惊吓测试对恐惧的敏感度高于基线变化。

方法

对恐惧条件化的大鼠使用Alzet渗透泵,每天给予0.25毫克/千克芬太尼或安慰剂泵。实验1研究阿片类药物治疗前及治疗期间在运动活动、基线、预脉冲抑制和恐惧增强惊吓反应方面的变化。实验2研究在4 - 7天治疗后使用静脉注射纳洛酮引发戒断期间的相同反应。

结果

实验1显示,芬太尼治疗开始后首次测试(4小时)时恐惧增强惊吓反应减弱;后续测试未出现此现象,提示对这种急性效应产生了耐受性。实验2发现,在芬太尼治疗的大鼠中,注射0.025毫克/千克和0.16毫克/千克纳洛酮后引发的恐惧增强惊吓反应增强;注射1毫克/千克纳洛酮时未出现此现象,尽管在此剂量下更多身体戒断症状最为普遍。在两个实验中,运动活动、基线ASR或ASR的预脉冲抑制均未显示出任何治疗效果。

结论

恐惧增强惊吓反应可能为药物戒断的类似焦虑效应提供一种特异且有效的衡量指标。讨论了出现此效应所需的条件以及这些发现与戒断不适不同机制的相关性。

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