Clark M, Dar M S
Department of Pharmacology, School of Medicine, East Carolina University, Greenville, NC 27858.
Life Sci. 1989;44(22):1625-35. doi: 10.1016/0024-3205(89)90479-7.
The effects of ethanol and adenosine receptor agonist R-PIA and antagonist theophylline on release of endogenous glutamate were tested in rat cerebellar synaptosomal preparation. Release was carried out for 5 to 60 sec after which time the released glutamate was separated from the synaptosomal membranes by rapid filtration. The amount of released glutamate in the filtrate was measured by an enzyme-linked fluorometric assay. Basal endogenous glutamate release was estimated as 3.7 +/- 0.3 nmol/mg protein/5 sec and was stimulated by high K+. Glutamate release consisted of an initial rapid phase for the first 10 sec that was followed by a relatively slower phase. Both Ca2+-dependent and Ca2+-independent glutamate release were observed which suggested the involvement of both neuronal and glial constituents of the synaptosomal preparation, respectively. Pharmacologically relevant concentrations of ethanol (25-100 mM) caused a trend toward a dose-dependent inhibition of glutamate release. R-PIA and theophylline inhibited and stimulated, respectively, basal release of glutamate and R-PIA-inhibited release was blocked by theophylline. Ethanol (25 mM) blocked the stimulatory effect of theophylline and the results of experiments following the inclusion of adenosine deaminase suggested the involvement of adenosine in this effect of ethanol. The results support our previous findings that suggest an involvement of cerebellar adenosine in the motor disturbing effects of acute ethanol and extend those findings by indicating that ethanol inhibits glutamate release from granule cells of the cerebellar cortex through an adenosine-sensitive mechanism.
在大鼠小脑突触体标本中测试了乙醇、腺苷受体激动剂R - PIA和拮抗剂茶碱对内源性谷氨酸释放的影响。释放过程持续5至60秒,之后通过快速过滤将释放的谷氨酸与突触体膜分离。滤液中释放的谷氨酸量通过酶联荧光测定法测量。基础内源性谷氨酸释放估计为3.7±0.3 nmol/mg蛋白质/5秒,并受到高钾离子的刺激。谷氨酸释放包括最初10秒的快速初始阶段,随后是相对较慢的阶段。观察到了钙离子依赖性和非钙离子依赖性谷氨酸释放,这分别表明突触体标本中的神经元和神经胶质成分都参与其中。药理学相关浓度的乙醇(25 - 100 mM)导致谷氨酸释放呈剂量依赖性抑制趋势。R - PIA和茶碱分别抑制和刺激谷氨酸的基础释放,且R - PIA抑制的释放被茶碱阻断。乙醇(25 mM)阻断了茶碱的刺激作用,并且在加入腺苷脱氨酶后的实验结果表明腺苷参与了乙醇的这种作用。这些结果支持了我们之前的发现,即小脑腺苷参与急性乙醇的运动干扰作用,并通过表明乙醇通过腺苷敏感机制抑制小脑皮质颗粒细胞的谷氨酸释放扩展了这些发现。