Nicholson R A, Liao C, Zheng J, David L S, Coyne L, Errington A C, Singh G, Lees G
Department of Biological Sciences, Simon Fraser University, 8888 University Drive, Burnaby, BC, Canada V5A 1S6.
Brain Res. 2003 Jul 18;978(1-2):194-204. doi: 10.1016/s0006-8993(03)02808-7.
Anandamide is a prominent member of the endocannabinoids, a group of diffusible lipid molecules which influences neuronal excitability. In this context, endocannabinoids are known to modulate certain presynaptic Ca(2+) and K(+) channels, either through cannabinoid (CB1) receptor stimulation and second messenger pathway activation or by direct action. We investigated the susceptibility of voltage-sensitive sodium channels to anandamide and other cannibimimetics using both biochemical and electrophysiological approaches. Here we report that anandamide, AM 404 and WIN 55,212-2 inhibit veratridine-dependent depolarization of synaptoneurosomes (IC(50)s, respectively 21.8, 9.3 and 21.1 microM) and veratridine-dependent release of L-glutamic acid and GABA from purified synaptosomes [IC(50)s: 5.1 microM (L-glu) and 16.5 microM (GABA) for anandamide; 1.6 microM (L-glu) and 3.3 microM (GABA) for AM 404, and 12.2 (L-glu) and 14.4 microM (GABA) for WIN 55,212-2]. The binding of [3H]batrachotoxinin A 20-alpha-benzoate to voltage-sensitive sodium channels was also inhibited by low to mid micromolar concentrations of anandamide, AM 404 and WIN 55,212-2. In addition, anandamide (10 microM), AM 404 (10 microM) and WIN 55,212-2 (1 microM) were found to markedly block TTX-sensitive sustained repetitive firing in cortical neurones without altering primary spikes, consistent with a state-dependent mechanism. None of the inhibitory effects we demonstrate on voltage-sensitive sodium channels are attenuated by the potent CB1 antagonist AM 251 (1-2 microM). Anandamide's action is reversible and its effects are enhanced by fatty acid amidohydrolase inhibition. We propose that voltage-sensitive sodium channels may participate in a novel signaling pathway involving anandamide. This mechanism has potential to depress synaptic transmission in brain by damping neuronal capacity to support action potentials and reducing evoked release of both excitatory and inhibitory transmitters.
花生四烯乙醇胺是内源性大麻素中的一种重要成分,内源性大麻素是一类可扩散的脂质分子,会影响神经元的兴奋性。在这种情况下,已知内源性大麻素可通过大麻素(CB1)受体刺激和第二信使途径激活,或直接作用来调节某些突触前Ca(2+)和K(+)通道。我们使用生化和电生理方法研究了电压敏感性钠通道对花生四烯乙醇胺和其他大麻模拟物的敏感性。在此我们报告,花生四烯乙醇胺、AM 404和WIN 55,212-2可抑制藜芦碱依赖性的突触神经体去极化(IC(50)分别为21.8、9.3和21.1 microM),以及藜芦碱依赖性的从纯化突触体中释放L-谷氨酸和GABA [IC(50):花生四烯乙醇胺对L-谷氨酸为5.1 microM,对GABA为16.5 microM;AM 404对L-谷氨酸为1.6 microM,对GABA为3.3 microM;WIN 55,212-2对L-谷氨酸为12.2 microM,对GABA为14.4 microM]。低至中微摩尔浓度的花生四烯乙醇胺、AM 404和WIN 55,212-2也可抑制[3H]蛙皮毒素A 20-α-苯甲酸酯与电压敏感性钠通道的结合。此外,发现花生四烯乙醇胺(10 microM)、AM 404(10 microM)和WIN 55,212-2(1 microM)可显著阻断皮层神经元中TTX敏感的持续重复放电,而不改变初级动作电位,这与一种状态依赖性机制一致。我们所证明的对电压敏感性钠通道的抑制作用均未被强效CB1拮抗剂AM 251(1-2 microM)减弱。花生四烯乙醇胺的作用是可逆的,并且其脂肪酸酰胺水解酶抑制作用可增强其效果。我们提出,电压敏感性钠通道可能参与了一条涉及花生四烯乙醇胺的新型信号通路。这种机制有可能通过抑制神经元支持动作电位的能力以及减少兴奋性和抑制性递质的诱发释放来抑制大脑中的突触传递。