Kruk-Slomka Marta, Boguszewska-Czubara Anna, Slomka Tomasz, Budzynska Barbara, Biala Grazyna
Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Chodzki 4a Street, 20-093 Lublin, Poland.
Department of Medical Chemistry, Medical University of Lublin, Chodzki 4a Street, 20-093 Lublin, Poland.
Neural Plast. 2016;2016:9815092. doi: 10.1155/2016/9815092. Epub 2015 Dec 29.
The endocannabinoid system, through cannabinoid (CB) receptors, is involved in memory-related responses, as well as in processes that may affect cognition, like oxidative stress processes. The purpose of the experiments was to investigate the impact of CB1 and CB2 receptor ligands on the long-term memory stages in male Swiss mice, using the passive avoidance (PA) test, as well as the influence of these compounds on the level of oxidative stress biomarkers in the mice brain. A single injection of a selective CB1 receptor antagonist, AM 251, improved long-term memory acquisition and consolidation in the PA test in mice, while a mixed CB1/CB2 receptor agonist WIN 55,212-2 impaired both stages of cognition. Additionally, JWH 133, a selective CB2 receptor agonist, and AM 630, a competitive CB2 receptor antagonist, significantly improved memory. Additionally, an acute administration of the highest used doses of JWH 133, WIN 55,212-2, and AM 630, but not AM 251, increased total antioxidant capacity (TAC) in the brain. In turn, the processes of lipids peroxidation, expressed as the concentration of malondialdehyde (MDA), were more advanced in case of AM 251. Thus, some changes in the PA performance may be connected with the level of oxidative stress in the brain.
内源性大麻素系统通过大麻素(CB)受体参与与记忆相关的反应,以及可能影响认知的过程,如氧化应激过程。本实验的目的是使用被动回避(PA)试验研究CB1和CB2受体配体对雄性瑞士小鼠长期记忆阶段的影响,以及这些化合物对小鼠大脑中氧化应激生物标志物水平的影响。单次注射选择性CB1受体拮抗剂AM 251可改善小鼠PA试验中的长期记忆获得和巩固,而CB1/CB2受体混合激动剂WIN 55,212-2则损害认知的两个阶段。此外,选择性CB2受体激动剂JWH 133和竞争性CB2受体拮抗剂AM 630可显著改善记忆。此外,急性给予最高使用剂量的JWH 133、WIN 55,212-2和AM 630(但不包括AM 251)可增加大脑中的总抗氧化能力(TAC)。反过来,以丙二醛(MDA)浓度表示的脂质过氧化过程在AM 251的情况下更为明显。因此,PA表现的一些变化可能与大脑中的氧化应激水平有关。