右美沙芬对大鼠甲基苯丙胺致药物寻找和行为致敏的后处理。

Synapse (New York, N.y.) Pub Date : 2012-10-01 Epub Date: 2012-06-26 DOI:10.1002/syn.21576
Pao-Pao Yang, Eagle Yi-Kung Huang, Yu-Ying Fu, Tsai-Shan Ho, Pao-Luh Tao
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引用次数: 5

摘要

在我们之前的研究中,我们首先证明了右美沙芬(DM)对吗啡依赖大鼠吗啡寻求行为的显著影响,当吗啡戒断时给予右美沙芬。采用同样的条件位置偏好(CPP)范式,我们进一步研究了DM对MA依赖大鼠甲基苯丙胺(MA)寻求的可能影响。我们的数据显示,在MA戒断期间服用右美沙芬也能有效抑制MA的觅药行为。这表明右美沙芬可能具有防止成瘾性药物寻求行为的药理学性质。为了检查DM在大脑中的作用部位,将DM微注射到VTA或NAc,并测试其对戒断期间ma寻求的影响。在vta内和nac内注射DM均能阻断ma寻找,提示DM具有双重作用位点。在我们的神经化学结果中,DM在NAc内注射显示出戒断期间对MA挑战的NAc和mPFC的DA周转率明显降低,这与行为结果相匹配。然而,vta内注射DM降低了mPFC的DA周转率,但对NAc的DA周转率没有影响。虽然我们的神经化学和行为结果之间的联系可能需要进一步的研究来验证,但本研究强调了DM在MA的抗药物寻求行为中的治疗潜力,其机制可能与其对中脑边缘和中脑皮层多巴胺能通路的影响有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-treatment of dextromethorphan on methamphetamine-induced drug-seeking and behavioral sensitization in rats.

In our previous study, we first demonstrated a significant effect of dextromethorphan (DM) on morphine-seeking behavior in morphine-dependent rats, when DM was given during morphine withdrawal. Using the same conditioned place preference (CPP) paradigm modified for measuring drug-seeking-related behavior, we further investigated the possible effect of DM on methamphetamine (MA)-seeking in MA-dependent rats. Our data showed that DM could also effectively suppress the drug-seeking behavior for MA, when administered during MA withdrawal. This suggests that DM may possess a pharmacological property to prevent drug-seeking behavior for addictive drugs in general. To examine the action sites of DM in the brain, DM was microinjected into the VTA or the NAc, and tested for its effect on MA-seeking during withdrawal. Both intra-VTA and intra-NAc injections of DM were able to block the MA-seeking, suggesting that DM has a dual action sites. In our neurochemical results, intra-NAc injection of DM showed a clear reduction of DA turnover rate at the NAc and the mPFC in response to MA challenge during withdrawal, which matched with the behavioral results. However, intra-VTA injection of DM reduced the DA turnover rate at the mPFC but did not have effect on the DA turnover rate at the NAc. Although further investigations may be needed to verify the connection between our neurochemical and behavioral results, the present study highlights the therapeutic potential of DM in antidrug-seeking behavior of MA and that the mechanism could be related to its effect on the mesolimbic and mesocortical dopaminergic pathways.

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