Raffa Robert B, Cavallo Federica, Capasso Anna
Department of Pharmaceutical Sciences, Temple University School of Pharmacy, 3307 N. Broad Street, Philadelphia, PA 19140, USA.
Eur J Pharmacol. 2007 Jun 14;564(1-3):88-93. doi: 10.1016/j.ejphar.2007.02.006. Epub 2007 Feb 16.
Two benzodiazepine (midazolam and clorazepate) and one non-benzodiazepine (zolpidem) benzodiazepine-receptor agonists produced dose-related physical dependence, as evidenced by abstinence-induced decrease in planarian locomotor velocity (pLMV) when drug-exposed planarians were placed into drug-free water, but not when they were placed into drug-containing water (i.e., an abstinence-induced withdrawal, since the effect was only obtained in the removal of drug and not in the continued presence of drug). We have previously shown that the decrease in pLMV is associated with specific and transient withdrawal signs. In the present study, the selective benzodiazepine-receptor antagonist flumazenil significantly antagonized (P<0.05), by co-application, the ability of each agonist to produce the withdrawal. These results: (1) suggest that benzodiazepine-receptor agonists, for two different chemical categories, produce dose-related physical dependence manifested as abstinence-induced withdrawal in this simple and convenient model, and (2) in the absence of cloning or radioligand binding literature, suggest a possible specific interaction site (receptor?) for these compounds in planarians.
两种苯二氮䓬类药物(咪达唑仑和氯氮䓬)以及一种非苯二氮䓬类药物(唑吡坦)这三种苯二氮䓬受体激动剂产生了剂量相关的身体依赖性,证据是当接触药物的涡虫被放入无药水中时,戒断诱导的涡虫运动速度(pLMV)降低,但当它们被放入含药水中时则不会(即戒断诱导的戒断反应,因为这种效应仅在去除药物时出现,而不是在药物持续存在时出现)。我们之前已经表明,pLMV的降低与特定的短暂戒断症状相关。在本研究中,选择性苯二氮䓬受体拮抗剂氟马西尼通过共同应用显著拮抗(P<0.05)了每种激动剂产生戒断反应的能力。这些结果:(1)表明两种不同化学类别的苯二氮䓬受体激动剂在这个简单便捷的模型中产生了剂量相关的身体依赖性,表现为戒断诱导的戒断反应;(2)在缺乏克隆或放射性配体结合文献的情况下,提示这些化合物在涡虫中可能存在一个特定的相互作用位点(受体?)。