College of Life Sciences and Key Laboratory of Modern Teaching Technology, Shaanxi Normal University, Xian, China.
Cell. 2012 Mar 2;148(5):1039-50. doi: 10.1016/j.cell.2012.01.037.
Impairment of working memory is one of the most important deleterious effects of marijuana intoxication in humans, but its underlying mechanisms are presently unknown. Here, we demonstrate that the impairment of spatial working memory (SWM) and in vivo long-term depression (LTD) of synaptic strength at hippocampal CA3-CA1 synapses, induced by an acute exposure of exogenous cannabinoids, is fully abolished in conditional mutant mice lacking type-1 cannabinoid receptors (CB(1)R) in brain astroglial cells but is conserved in mice lacking CB(1)R in glutamatergic or GABAergic neurons. Blockade of neuronal glutamate N-methyl-D-aspartate receptors (NMDAR) and of synaptic trafficking of glutamate α-amino-3-hydroxy-5-methyl-isoxazole propionic acid receptors (AMPAR) also abolishes cannabinoid effects on SWM and LTD induction and expression. We conclude that the impairment of working memory by marijuana and cannabinoids is due to the activation of astroglial CB(1)R and is associated with astroglia-dependent hippocampal LTD in vivo.
工作记忆损伤是大麻中毒对人类产生的最重要的有害影响之一,但目前其潜在机制尚不清楚。在这里,我们证明了由外源性大麻素急性暴露引起的空间工作记忆(SWM)损伤和海马 CA3-CA1 突触处突触强度的体内长时程抑制(LTD),在大脑星形胶质细胞中缺乏 1 型大麻素受体(CB1R)的条件性突变小鼠中完全消除,但在缺乏谷氨酸能或 GABA 能神经元中 CB1R 的小鼠中保留。阻断神经元谷氨酸 N-甲基-D-天冬氨酸受体(NMDAR)和谷氨酸 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)的突触转运也消除了大麻素对 SWM 和 LTD 诱导和表达的影响。我们得出结论,大麻和大麻素对工作记忆的损伤是由于星形胶质细胞 CB1R 的激活所致,并且与体内星形胶质细胞依赖性海马 LTD 相关。