Department of Psychological and Brain Sciences, Boston University, Boston, USA; Center for Systems Neuroscience, Boston University, Boston, USA.
Department of Psychological and Brain Sciences, Boston University, Boston, USA.
Behav Brain Res. 2020 Oct 1;395:112839. doi: 10.1016/j.bbr.2020.112839. Epub 2020 Aug 2.
Brief interventions of environmental enrichment (EE) or the glycine transporter-1 inhibitor Org24598 administered with cocaine-cue extinction training were shown previously to inhibit reacquisition of cocaine self-administration in male rats trained to self-administer a moderate 0.3 mg/kg dose of cocaine. Determining how EE and Org24598 synergize in combination in an animal model of cue exposure therapy is novel. Important changes made in this investigation were increasing the cocaine training dose to 1.0 mg/kg and determining sex differences. Adult male and female rats self-administering 1.0 mg/kg cocaine for 35-40 daily sessions exhibited an addiction-like phenotype under a second-order schedule of cocaine delivery and cue presentation. Rats next underwent 6 weekly extinction training sessions for which treatments consisted of EE or NoEE and Vehicle or Org24598 (3.0 mg/kg in males; 3.0 or 7.5 mg/kg in females). Rats then were tested for reacquisition of cocaine self-administration for 15 daily sessions. In males, the combined EE +3.0 mg/kg Org24598 treatment facilitated extinction learning and inhibited reacquisition of cocaine self-administration to a greater extent than no treatment and to individual EE or 3.0 mg/kg Org24598 treatments. In females, EE +7.5 mg/kg Org24598 facilitated extinction learning, but did not inhibit reacquisition of cocaine self-administration. Thus, there were sex differences in the ability of EE + Org24598 administered in conjunction with extinction training to inhibit cocaine relapse in rats exhibiting an addiction-like phenotype. These findings suggest that this multimodal treatment approach might be a feasible option during cue exposure therapy in cocaine-dependent men, but not women.
以前的研究表明,环境富集(EE)或甘氨酸转运体-1 抑制剂 Org24598 的简短干预措施,与可卡因线索消退训练一起使用,可以抑制在接受中等剂量 0.3 毫克/千克可卡因自我给药训练的雄性大鼠中可卡因自我给药的重新获得。在暴露于线索的动物模型中,确定 EE 和 Org24598 如何协同作用是新颖的。在这项研究中,进行了重要的改变,将可卡因训练剂量增加到 1.0 毫克/千克,并确定了性别差异。接受 1.0 毫克/千克可卡因 35-40 天的成年雄性和雌性大鼠,在可卡因给予和线索呈现的二阶时间表下表现出类似成瘾的表型。然后,大鼠接受了 6 周的消退训练,治疗方法包括 EE 或无 EE 和载体或 Org24598(雄性 3.0 毫克/千克;雌性 3.0 或 7.5 毫克/千克)。然后,大鼠进行了 15 天的可卡因自我给药重新获得测试。在雄性中,联合 EE +3.0 毫克/千克 Org24598 治疗促进了消退学习,并比不治疗和单独 EE 或 3.0 毫克/千克 Org24598 治疗更能抑制可卡因自我给药的重新获得。在雌性中,EE +7.5 毫克/千克 Org24598 促进了消退学习,但没有抑制可卡因自我给药的重新获得。因此,在表现出类似成瘾的表型的大鼠中,EE +Org24598 与消退训练联合给药抑制可卡因复吸的能力存在性别差异。这些发现表明,这种多模式治疗方法可能是可卡因依赖男性在暴露于线索治疗期间的可行选择,但不是女性。