Department of Pharmacology, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Synapse. 2012 Oct;66(10):858-69. doi: 10.1002/syn.21576. Epub 2012 Jun 26.
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.
在我们之前的研究中,我们首先证明了右美沙芬(DM)在吗啡依赖大鼠吗啡戒断期间给药时对吗啡觅药行为有显著影响。使用相同的条件位置偏好(CPP)范式修改来测量与药物寻求相关的行为,我们进一步研究了 DM 对 MA 依赖大鼠 MA 觅药的可能影响。我们的数据表明,DM 也可以在 MA 戒断期间给药时有效抑制 MA 的觅药行为。这表明 DM 可能具有预防一般成瘾药物觅药行为的药理学特性。为了研究 DM 在大脑中的作用部位,将 DM 微注射到 VTA 或 NAc 中,并测试其在戒断期间对 MA 觅药的作用。VTA 内和 NAc 内注射 DM 均可阻断 MA 觅药,表明 DM 具有双重作用部位。在我们的神经化学结果中,DM 内注射到 NAc 可明显降低 MA 戒断期间刺激引起的 NAc 和 mPFC 中的 DA 周转率,与行为结果相符。然而,VTA 内注射 DM 降低了 mPFC 中的 DA 周转率,但对 NAc 中的 DA 周转率没有影响。尽管可能需要进一步的研究来验证我们的神经化学和行为结果之间的联系,但本研究强调了 DM 在抗 MA 觅药行为中的治疗潜力,其机制可能与其对中脑边缘和中脑皮质多巴胺能通路的影响有关。