Cross state-dependent memory retrieval between tramadol and ethanol: involvement of dorsal hippocampal GABAA receptors

• Published in: Psychopharmacology Vol. 241; no. 1; pp. 139 - 152
• Main Authors: Jafari-Sabet, Majid, Amiri, Shiva, Sheibani, Mohammad, Fatahi, Navid, Aghamiri, Helia
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 2024; Springer Nature B.V
• Subjects: Amnesia; Amnesia - chemically induced; Amnesia - metabolism; Animals; Avoidance Learning; Bicuculline; Biomedical and Life Sciences; Biomedicine; CA1 Region, Hippocampal; Drug addiction; Drug dosages; Ethanol; Ethanol - pharmacology; Hippocampus; Hypotheses; Injection; Memory; Mice; Mice, Inbred Strains; Neurosciences; Neurotransmission; Original Investigation; Pharmacology/Toxicology; Psychiatry; Receptors, GABA-A - metabolism; Tramadol; Tramadol - pharmacology; γ-Aminobutyric acid A receptors; State-dependent memory; Ethanol; Mouse; Tramadol; Bicuculline; Dorsal hippocampus
• ISSN: 0033-3158; 1432-2072
• DOI: 10.1007/s00213-023-06469-6

Rationale 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. Objective 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. Results 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. Conclusion 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.