Department of Drug Dependence Research, National Institute of Mental Health, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-higashi, Kodaira, Tokyo 187-8553, Japan.
Department of Drug Dependence Research, National Institute of Mental Health, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-higashi, Kodaira, Tokyo 187-8553, Japan.
Toxicol Appl Pharmacol. 2020 Dec 1;408:115283. doi: 10.1016/j.taap.2020.115283. Epub 2020 Oct 15.
Marijuana or synthetic cannabinoids and alcohol are often used together, with these combinations causing motor impairments that can subsequently lead to motor vehicle accidents. This study investigated the combined use of both synthetic cannabinoids and ethanol and their effect on motor coordination in mice in addition to examining the neurochemical changes in the cerebellum. Ethanol (2 g/kg, i.p.) significantly induced motor impairment in the accelerating rotarod test in mice. Furthermore, ethanol-induced motor impairments were further accentuated when combined with the synthetic cannabinoid, JWH-018 or AB-CHMINACA. The enhancement effects of the synthetic cannabinoids were completely antagonized by pretreatment with the selective CB receptor antagonist AM251, but not by the selective CB receptor antagonist AM630. Neurochemical study results showed that ethanol caused a reduction in the extracellular glutamate levels in the cerebellum during periods of ethanol-induced motor impairment. In addition to the enhanced motor impairment seen when ethanol was combined with JWH-018, these combinations also enhanced the reduction of the extracellular glutamate levels in the cerebellum. We additionally used microelectrode array recordings to examine the effects of ethanol and/or JWH-018 on the spontaneous network activity in primary cultures from mouse cerebellum. Results showed that ethanol combined with JWH-018 significantly reduced spontaneous neuronal network activity in the primary cerebellar culture. Our findings demonstrate that ethanol-induced motor impairments are enhanced by synthetic cannabinoids, with these effects potentially mediated by CB receptors. An accentuated reduction of neurotransmissions in the cerebellum may play an important role in motor impairments caused by ethanol combined with synthetic cannabinoids.
大麻或合成大麻素和酒精经常一起使用,这些组合会导致运动障碍,进而导致机动车事故。本研究调查了合成大麻素和乙醇的联合使用及其对小鼠运动协调的影响,此外还研究了小脑的神经化学变化。乙醇(2 g/kg,ip)显著诱导小鼠加速旋转棒测试中的运动障碍。此外,当与合成大麻素 JWH-018 或 AB-CHMINACA 联合使用时,乙醇引起的运动障碍进一步加重。合成大麻素的增强作用完全被选择性 CB 受体拮抗剂 AM251 预处理所拮抗,但不被选择性 CB 受体拮抗剂 AM630 拮抗。神经化学研究结果表明,乙醇在引起运动障碍期间导致小脑细胞外谷氨酸水平降低。除了与 JWH-018 联合使用时观察到的增强运动障碍外,这些组合还增强了小脑细胞外谷氨酸水平的降低。我们还使用微电极阵列记录来检查乙醇和/或 JWH-018 对来自小鼠小脑的原代培养物中自发性网络活动的影响。结果表明,乙醇与 JWH-018 联合显著降低了原代小脑培养物中的自发性神经元网络活动。我们的研究结果表明,乙醇诱导的运动障碍被合成大麻素增强,这些作用可能由 CB 受体介导。小脑神经传递的明显减少可能在乙醇与合成大麻素联合引起的运动障碍中发挥重要作用。