Department of Psychobiology, Facultad de Psicología, Universitat de València, Avda. Blasco Ibáñez 21, 46010, Valencia, Spain.
Department of Physiology, School of Medicine, Universitat de Valencia, Avda. Blasco Ibáñez, 15, 46010, Valencia, Spain.
Behav Brain Funct. 2023 May 24;19(1):8. doi: 10.1186/s12993-023-00210-1.
The lipid oleoylethanolamide (OEA) has been shown to affect reward-related behavior. However, there is limited experimental evidence about the specific neurotransmission systems OEA may be affecting to exert this modulatory effect. The aim of this study was to evaluate the effects of OEA on the rewarding properties of cocaine and relapse-related gene expression in the striatum and hippocampus. For this purpose, we evaluated male OF1 mice on a cocaine-induced CPP procedure (10 mg/kg) and after the corresponding extinction sessions, we tested drug-induced reinstatement. The effects of OEA (10 mg/kg, i.p.) were evaluated at three different timepoints: (1) Before each cocaine conditioning session (OEA-C), (2) Before extinction sessions (OEA-EXT) and (3) Before the reinstatement test (OEA-REINST). Furthermore, gene expression changes in dopamine receptor D1 gene, dopamine receptor D2 gene, opioid receptor µ, cannabinoid receptor 1, in the striatum and hippocampus were analyzed by qRT-PCR. The results obtained in the study showed that OEA administration did not affect cocaine CPP acquisition. However, mice receiving different OEA treatment schedules (OEA-C, OEA-EXT and OEA-REINST) failed to display drug-induced reinstatement. Interestingly, the administration of OEA blocked the increase of dopamine receptor gene D1 in the striatum and hippocampus caused by cocaine exposure. In addition, OEA-treated mice exhibited reduced striatal dopamine receptor gene D2 and cannabinoid receptor 1. Together, these findings suggest that OEA may be a promising pharmacological agent in the treatment of cocaine use disorder.
油酰乙醇酰胺(OEA)已被证明会影响与奖励相关的行为。然而,关于 OEA 可能影响的特定神经传递系统以发挥这种调节作用的实验证据有限。本研究的目的是评估 OEA 对可卡因的奖赏特性和纹状体和海马中与复发相关的基因表达的影响。为此,我们在可卡因诱导的 CPP 程序(10mg/kg)中评估了雄性 OF1 小鼠,并且在相应的消退阶段之后,我们测试了药物诱导的复吸。OEA(10mg/kg,ip)的作用在三个不同时间点进行评估:(1)在每次可卡因条件作用阶段之前(OEA-C),(2)在消退阶段之前(OEA-EXT)和(3)在复吸测试之前(OEA-REINST)。此外,通过 qRT-PCR 分析了纹状体和海马中的多巴胺受体 D1 基因、多巴胺受体 D2 基因、阿片受体µ、大麻素受体 1 的基因表达变化。研究结果表明,OEA 给药不会影响可卡因 CPP 的获得。然而,接受不同 OEA 治疗方案(OEA-C、OEA-EXT 和 OEA-REINST)的小鼠未能显示出药物诱导的复吸。有趣的是,OEA 的给药阻止了可卡因暴露引起的纹状体和海马中多巴胺受体基因 D1 的增加。此外,OEA 处理的小鼠表现出纹状体多巴胺受体基因 D2 和大麻素受体 1 的减少。总之,这些发现表明 OEA 可能是治疗可卡因使用障碍的有前途的药物。