Department of Psychiatry, Division of Neuroscience, New England Primate Research Center, Beth Israel Deaconess Medical Center and Harvard Medical School, MA 01772, USA.
Neuropsychopharmacology. 2013 May;38(6):1006-14. doi: 10.1038/npp.2012.265. Epub 2012 Dec 27.
Benzodiazepines are prescribed widely but their utility is limited by unwanted side effects, including abuse potential. The mechanisms underlying the abuse-related effects of benzodiazepines are not well understood, although α1 subunit-containing GABAA receptors have been proposed to have a critical role. Here, we examine the reinforcing effects of several compounds that vary with respect to intrinsic efficacy at α2, α3, and α5 subunit-containing GABAA receptors but lack efficacy at α1 subunit-containing GABAA receptors ('α1-sparing compounds'): MRK-623 (functional selectivity for α2/α3 subunit-containing receptors), TPA023B (functional selectivity for α2/α3/α5 subunit-containing receptors), and TP003 (functional selectivity for α3 subunit-containing receptors). The reinforcing effects of the α1-sparing compounds were compared with those of the non-selective benzodiazepine receptor partial agonist MRK-696, and non-selective benzodiazepine receptor full agonists, midazolam and lorazepam, in rhesus monkeys trained to self-administer midazolam or cocaine, under a progressive-ratio schedule of intravenous (i.v.) drug injection. The α1-sparing compounds were self-administered significantly above vehicle levels in monkeys maintained under a midazolam baseline, but not under a cocaine baseline over the dose ranges tested. Importantly, TP003 had significant reinforcing effects, albeit at lower levels of self-administration than non-selective benzodiazepine receptor agonists. Together, these results suggest that α1 subunit-containing GABAA receptors may have a role in the reinforcing effects of benzodiazepine-type compounds in monkeys with a history of stimulant self-administration, whereas α3 subunit-containing GABAA receptors may be important mediators of the reinforcing effects of benzodiazepine-type compounds in animals with a history of sedative-anxiolytic/benzodiazepine self-administration.
苯二氮䓬类药物被广泛应用,但由于其副作用,包括滥用潜力,其应用受到限制。虽然含有α1 亚基的 GABA A 受体被认为具有关键作用,但苯二氮䓬类药物与滥用相关的作用机制尚未得到很好的理解。在这里,我们研究了几种化合物的强化作用,这些化合物在含有 α2、α3 和 α5 亚基的 GABA A 受体方面的内在效力不同,但在含有 α1 亚基的 GABA A 受体方面缺乏效力(“α1 节约化合物”):MRK-623(功能性选择性 α2/α3 亚基受体)、TPA023B(功能性选择性 α2/α3/α5 亚基受体)和 TP003(功能性选择性 α3 亚基受体)。将 α1 节约化合物的强化作用与非选择性苯二氮䓬受体部分激动剂 MRK-696、非选择性苯二氮䓬受体完全激动剂咪达唑仑和劳拉西泮的强化作用进行了比较,这些化合物在接受过咪达唑仑或可卡因自我给药训练的恒河猴中,根据静脉(i.v.)药物注射的递增比率方案进行。在接受咪达唑仑基线的猴子中,α1 节约化合物在猴子中的自我给药水平明显高于载体水平,但在接受可卡因基线的猴子中,在测试的剂量范围内没有自我给药。重要的是,TP003 具有显著的强化作用,尽管自我给药水平低于非选择性苯二氮䓬受体激动剂。综上所述,这些结果表明,在有兴奋剂自我给药史的猴子中,含有 α1 亚基的 GABA A 受体可能在苯二氮䓬类化合物的强化作用中起作用,而含有 α3 亚基的 GABA A 受体可能在有镇静-抗焦虑/苯二氮䓬类自我给药史的动物中对苯二氮䓬类化合物的强化作用具有重要的介导作用。