Harris R A, Hood W F
J Pharmacol Exp Ther. 1980 Jun;213(3):562-8.
In vitro addition of ethanol or pentobarbital to synaptosomes isolated from rat or mouse brain inhibited the depolarization-dependent uptake of calcium without affecting uptake under nondepolarizing conditions. Ethanol inhibited the uptake in a concentration-dependent manner over the range of 45 to 720 mM. Analysis of the effects of ethanol and pentobarbital on calcium uptake at different temperatures indicated that the drugs did not change the activation energy of the process but shifted the Arrhenius curves toward higher temperatures. Synaptosomes isolated from mice chronically ingesting ethanol were found to be tolerant to the inhibitory effects of ethanol and pentobarbital but not tolerant to the inhibitory effects of acetaldehyde. Synaptosomes from ethanol tolerant-dependent mice accumulated less calcium in the absence of ethanol than did synaptosomes from control mice. This depression of uptake was reversed by in vitro exposure of the synaptosomes to a low concentration of ethanol, suggesting that it represents a biochemical response to withdrawal of alcohol. A single acute injection of ethanol 1 hr before sacrifice did not alter the calcium uptake activity or the drug sensitivity of the synaptosomes. These results suggest that the known inhibitory effects of ethanol and pentobarbital on the stimulated release of neurotransmitters and the development of tolerance of these effects may be mediated by the inhibition of the depolarization-dependent influx of calcium by these drugs.
在从大鼠或小鼠脑部分离出的突触体中体外添加乙醇或戊巴比妥,会抑制去极化依赖性钙摄取,而不影响非去极化条件下的摄取。乙醇在45至720 mM范围内以浓度依赖性方式抑制摄取。对乙醇和戊巴比妥在不同温度下对钙摄取的影响分析表明,这些药物不会改变该过程的活化能,但会将阿累尼乌斯曲线移向更高温度。发现长期摄入乙醇的小鼠分离出的突触体对乙醇和戊巴比妥的抑制作用具有耐受性,但对乙醛的抑制作用不耐受。在无乙醇的情况下,来自乙醇耐受性依赖小鼠的突触体比来自对照小鼠的突触体积累的钙更少。突触体在体外暴露于低浓度乙醇后,这种摄取抑制作用得到逆转,表明这代表了对戒酒的生化反应。在处死前1小时单次急性注射乙醇不会改变突触体的钙摄取活性或药物敏感性。这些结果表明,乙醇和戊巴比妥对神经递质刺激释放的已知抑制作用以及对这些作用的耐受性发展可能是由这些药物抑制去极化依赖性钙内流介导的。