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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Additive effect of stress and drug cues on reinstatement of ethanol seeking: exacerbation by history of dependence and role of concurrent activation of corticotropin-releasing factor and opioid mechanisms.
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Additive effect of stress and drug cues on reinstatement of ethanol seeking: exacerbation by history of dependence and role of concurrent activation of corticotropin-releasing factor and opioid mechanisms.

机译:压力和药物提示对寻求乙醇的恢复的累加作用:因依赖史以及促肾上腺皮质激素释放因子和阿片类物质机制同时激活的作用而加剧。

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摘要

Stress and exposure to drug-related environmental stimuli have been implicated as critical factors in relapse to drug use. What has received little attention, however, is the significance of interactions between these factors for motivating drug-seeking behavior. To address this issue, a reinstatement model of relapse was used. Footshock stress and response-contingent presentation of an ethanol-associated light cue, acting as a conditioned stimulus (CS), effectively reinstated extinguished responding at a previously active, drug-paired lever in male Wistar rats. When response-contingent availability of the ethanol CS was preceded by footshock, additive effects of these stimuli on responding were observed. Both the individual and interactive effects of footshock and the CS were significantly greater in previously ethanol-dependent than in nondependent rats. Responding induced by the ethanol CS was selectively reversed by the nonselective opiate antagonist naltrexone, whereas the effects of footshock were selectively reversed by the corticotropin-releasing factor (CRF) antagonist d-Phe-CRF(12-41). However, both agents only partially reversed the enhanced drug-seeking response produced by the interactive effects of stress and the ethanol CS; full reversal required coadministration of d-Phe-CRF and naltrexone. The results document that stress and drug-related environmental stimuli interact to augment the resumption of drug seeking after extinction and suggest that this effect results from concurrent activation of opioid and CRF transmission.
机译:压力和暴露于药物相关的环境刺激已被认为是药物使用复发的关键因素。然而,很少引起注意的是这些因素之间的相互作用对于激发药物寻找行为的重要性。为了解决此问题,使用了恢复复发的模型。休克应激和乙醇相关的光提示,作为条件性刺激(CS),可有效恢复雄性Wistar大鼠在先前活跃的,与药物配对的杠杆作用下的熄灭反应。当发生休克之前,乙醇CS的响应可能获得可用性时,观察到了这些刺激对响应的累加效应。在以前乙醇依赖的情况下,休克和CS的个体和交互作用均显着大于非依赖大鼠。非选择性阿片拮抗剂纳曲酮可选择性逆转乙醇CS诱导的反应,而促肾上腺皮质激素释放因子(CRF)拮抗剂d-Phe-CRF(12-41)可选择性逆转足触的影响。然而,两种药物仅部分逆转了由应激和乙醇CS相互作用产生的增强的寻求药物反应。完全逆转需要d-Phe-CRF和纳曲酮共同给药。结果表明,压力和与药物有关的环境刺激相互作用,以增强灭绝后寻求药物的恢复,并表明这种作用是由同时激活阿片类药物和CRF传播引起的。

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