Razi Drug Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Department of Pharmacology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Psychopharmacology (Berl). 2024 Jan;241(1):139-152. doi: 10.1007/s00213-023-06469-6. Epub 2023 Sep 27.
Tramadol and ethanol, as psychoactive agents, are often abused. Discovering the molecular pathways of drug-induced memory creation may contribute to preventing drug addiction and relapse.
The tramadol- and ethanol-induced state-dependent memory (SDM) and cross-SDM retrieval between tramadol and ethanol were examined in this study. Moreover, because of the confirmed involvement of GABAA receptors and GABAergic neurotransmission in memory retrieval impairment, we assessed cross-SDM retrieval between tramadol and ethanol with a specific emphasis on the role of the GABAA receptors. The first hypothesis of this study was the presence of cross-SDM between tramadol and ethanol, and the second hypothesis was related to possible role of GABAA receptors in memory retrieval impairment within the dorsal hippocampus. The cannulae were inserted into the hippocampal CA1 area of NMRI mice, and a step-down inhibitory avoidance test was used to evaluate state dependence and memory recovery.
The post-training and/or pre-test administration of tramadol (2.5 and 5 mg/kg, i.p.) and/or ethanol (0.5 and 1 g/kg, i.p.) induced amnesia, which was restored after the administration of the drugs 24 h later during the pre-test period, proposing ethanol and tramadol SDM. The pre-test injection of ethanol (0.25 and 0.5 g/kg, i.p.) with tramadol at an ineffective dose (1.25 mg/kg) enhanced tramadol SDM. Moreover, tramadol injection (1.25 and 2.5 mg/kg) with ethanol at the ineffective dose (0.25 g/kg) promoted ethanol SDM. Furthermore, the pre-test intra-CA1 injection of bicuculline (0.0625, 0.125, and 0.25 μg/mouse), a GABAA receptor antagonist, 5 min before the injection of tramadol (5 mg/kg) or ethanol (1 g/kg) inhibited tramadol- and ethanol-induced SDM dose-dependently.
The findings strongly confirmed cross-SDM between tramadol and ethanol and the critical role of dorsal hippocampal GABAA receptors in the cross-SDM between tramadol and ethanol.
曲马多和乙醇作为精神活性物质,经常被滥用。发现药物诱导记忆产生的分子途径可能有助于预防药物成瘾和复发。
本研究旨在检测曲马多和乙醇诱导的状态依赖记忆(SDM)和曲马多与乙醇之间的交叉 SDM 检索。此外,由于 GABAA 受体和 GABA 能神经传递在记忆检索损伤中的作用已被证实,我们特别评估了曲马多和乙醇之间的交叉 SDM 检索,重点研究 GABAA 受体的作用。本研究的第一个假设是曲马多和乙醇之间存在交叉 SDM,第二个假设是 GABAA 受体在背侧海马记忆检索损伤中的可能作用。将导管插入 NMRI 小鼠的海马 CA1 区,使用下台阶抑制回避测试评估状态依赖性和记忆恢复。
曲马多(2.5 和 5 mg/kg,ip)和/或乙醇(0.5 和 1 g/kg,ip)在训练后和/或预测试时给药会导致健忘症,在预测试期间,在 24 小时后给予药物后会恢复,提出了乙醇和曲马多 SDM。预测试时给予无效剂量的曲马多(1.25 mg/kg)与乙醇(0.25 和 0.5 g/kg,ip)联合注射增强了曲马多 SDM。此外,给予无效剂量的乙醇(0.25 g/kg)与曲马多(1.25 和 2.5 mg/kg)联合注射促进了乙醇 SDM。此外,在注射曲马多(5 mg/kg)或乙醇(1 g/kg)前 5 分钟,在 CA1 内注射荷包牡丹碱(0.0625、0.125 和 0.25 μg/只),一种 GABAA 受体拮抗剂,可剂量依赖性地抑制曲马多和乙醇诱导的 SDM。
这些发现有力地证实了曲马多和乙醇之间的交叉 SDM,以及背侧海马 GABAA 受体在曲马多和乙醇之间的交叉 SDM 中的关键作用。