Rawls Scott M, Gomez Teresa, Raffa Robert B
Department of Pharmaceutical Sciences, Temple University School of Pharmacy, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Pharmacol Biochem Behav. 2007 Mar;86(3):499-504. doi: 10.1016/j.pbb.2007.01.010. Epub 2007 Jan 20.
The mechanisms that facilitate the development and expression of cannabinoid physical dependence in humans and other mammals are poorly understood. The present experiments used a planarian model to provide evidence that pharmacological antagonism of NMDA receptors significantly attenuates the development of cannabinoid physical dependence. Abstinence-induced withdrawal from the cannabinoid agonist WIN 55212-2 (10 microM) was manifested as a significant (P<0.05) decrease in the rate of planarian spontaneous locomotor velocity (pLMV) when WIN 55212-2 (10 microM)-exposed planarians were placed into drug-free water. No change in pLMV occurred when WIN 55212-2 (10 microM)-exposed planarians were placed into water containing WIN 55212-2 (10 microM). WIN 55212-2 (10 microM)-exposed planarians placed into water containing LY 235959 (1 or 10 microM) did not display withdrawal (no significant difference, P>0.05, in pLMV). In addition, withdrawal was not observed (no significant difference, P>0.05, in pLMV) in planarians that were co-exposed to a solution containing WIN 55212-2 (10 microM) and LY 235959 (10 microM). The present results reveal that NMDA receptor activation mediates the development of cannabinoid physical dependence and the expression of cannabinoid withdrawal in planarians.
促进人类和其他哺乳动物中大麻素身体依赖性发展和表现的机制目前仍知之甚少。本实验使用涡虫模型来提供证据,证明NMDA受体的药理学拮抗作用可显著减弱大麻素身体依赖性的发展。当将暴露于WIN 55212-2(10微摩尔)的涡虫放入无药水中时,从大麻素激动剂WIN 55212-2(10微摩尔)戒断诱导的戒断表现为涡虫自发运动速度(pLMV)显著降低(P<0.05)。当将暴露于WIN 55212-2(10微摩尔)的涡虫放入含有WIN 55212-2(10微摩尔)的水中时,pLMV没有变化。将暴露于WIN 55212-2(10微摩尔)的涡虫放入含有LY 235959(1或10微摩尔)的水中时,未表现出戒断(pLMV无显著差异,P>0.05)。此外,在同时暴露于含有WIN 55212-2(10微摩尔)和LY 235959(10微摩尔)溶液的涡虫中也未观察到戒断(pLMV无显著差异,P>0.05)。目前的结果表明,NMDA受体激活介导了涡虫中大麻素身体依赖性的发展和大麻素戒断的表现。