Listos Joanna, Talarek Sylwia, Fidecka Sylwia
Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Staszica 4, 20-081 Lublin, Poland.
Eur J Pharmacol. 2008 Jun 24;588(1):72-7. doi: 10.1016/j.ejphar.2008.04.011. Epub 2008 Apr 8.
In the present study, the effects of adenosine agonists on the development of sensitization to withdrawal signs precipitated after sporadic treatment with diazepam, in mice, were investigated. To obtain the sensitization, the animals were divided into groups: continuously and sporadically treated with diazepam (15.0 mg/kg, s.c.). The adenosine receptor agonists (CPA, CGS 21,680 and NECA) were administered in sporadically diazepam treated mice during two diazepam-free periods. Concomitant administration of pentetrazole (55.0 mg/kg, s.c.) with flumazenil (5.0 mg/kg, i.p.) after the last injection of diazepam or vehicle, induced the withdrawal signs, such as clonic seizures, tonic convulsion and death episodes. The major finding of our experiments is attenuation of withdrawal signs in sensitized mice, inducing by all adenosine agonists. Only higher dose of CPA produced significantly decreased the number of withdrawal incidents, while both used doses of CGS 21,680 and NECA produced more clear effects. These results support the hypothesis that adenosinergic system is involved in the mechanisms of sensitization to the benzodiazepine withdrawal signs, and adenosine A(2A) receptors play more important role in that process.
在本研究中,研究了腺苷激动剂对小鼠间歇性给予地西泮后诱发的戒断症状敏化发展的影响。为了诱导敏化,将动物分为几组:持续和间歇性给予地西泮(15.0 mg/kg,皮下注射)。在间歇性给予地西泮的小鼠的两个无地西泮期间,给予腺苷受体激动剂(CPA、CGS 21,680和NECA)。在最后一次注射地西泮或赋形剂后,将戊四氮(55.0 mg/kg,皮下注射)与氟马西尼(5.0 mg/kg,腹腔注射)联合使用,诱发戒断症状,如阵挛性惊厥、强直性惊厥和死亡发作。我们实验的主要发现是,所有腺苷激动剂均可减轻敏化小鼠的戒断症状。只有较高剂量的CPA显著减少了戒断事件的数量,而所用剂量的CGS 21,680和NECA均产生了更明显的效果。这些结果支持了以下假设:腺苷能系统参与了对苯二氮䓬类戒断症状敏化的机制,且腺苷A(2A)受体在该过程中发挥了更重要的作用。