Kruk-Slomka Marta, Biala Grażyna
Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Chodzki 4a Street, 20-093 Lublin, Poland.
Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Chodzki 4a Street, 20-093 Lublin, Poland.
Behav Brain Res. 2016 Mar 15;301:84-95. doi: 10.1016/j.bbr.2015.12.023. Epub 2015 Dec 19.
The endocannabinoid system, through the cannabinoid type 1 (CB1) and 2 (CB2) receptors modulates many physiological functions, including different aspects of memory-related processes. The aim of the present experiments was to explore the role of the endocannabinoid system, through CB1 receptors in the different stages of short-term (acquisition, retention and retrieval) and long-term (acquisition, consolidation and retrieval) memory-related responses, using the inhibitory avoidance (IA) test in mice. Our results revealed that an acute injection of oleamide (10 and 20mg/kg), a CB1 receptor agonist, impairs the short-term or/and long-term acquisition, retention/consolidation, retrieval memory and learning processes in the IA test in mice. In turn, in this test an acute injection of AM 251 (1 and 3mg/kg), a CB1 receptor antagonist, improves the short-term or/and long-term memory stages, described above. Moreover, this memory impairment induced by effective dose of oleamide (20mg/kg) is reversed by non-effective dose of AM 251 (0.25mg/kg) in the IA task, which proves the selectivity of oleamide to CB1 receptors and confirms that the CB1 receptor-related mechanism is one of the possible mechanisms, responsible for memory and learning responses. Obtained results provide clear evidence that the endocannabinoid system, through CB1 receptors, participates in the different stages of short- and long-term memory-related behavior. This knowledge may open in the future new possibilities for the development of CB-based therapies, especially for memory impairment human disorders.
内源性大麻素系统通过1型(CB1)和2型(CB2)大麻素受体调节许多生理功能,包括记忆相关过程的不同方面。本实验的目的是通过CB1受体,利用小鼠抑制性回避(IA)试验,探索内源性大麻素系统在短期(获取、保持和提取)和长期(获取、巩固和提取)记忆相关反应不同阶段中的作用。我们的结果显示,急性注射CB1受体激动剂油酰胺(10和20mg/kg)会损害小鼠IA试验中的短期或/和长期获取、保持/巩固、提取记忆及学习过程。反之,在该试验中,急性注射CB1受体拮抗剂AM 251(1和3mg/kg)可改善上述短期或/和长期记忆阶段。此外,在IA任务中,无效剂量的AM 251(0.25mg/kg)可逆转有效剂量油酰胺(20mg/kg)诱导的记忆损伤,这证明了油酰胺对CB1受体的选择性,并证实与CB1受体相关的机制是负责记忆和学习反应的可能机制之一。所得结果提供了明确证据,表明内源性大麻素系统通过CB1受体参与短期和长期记忆相关行为的不同阶段。这一知识未来可能为基于CB的疗法开发带来新的可能性,尤其是针对人类记忆障碍疾病。