Greenberg D A, Cooper E C
Alcohol Clin Exp Res. 1984 Nov-Dec;8(6):568-71. doi: 10.1111/j.1530-0277.1984.tb05732.x.
We examined the effect of ethanol on [3H]nitrendipine binding to rat brain membranes, to investigate the possibility that voltage-dependent calcium channels are involved in synaptic actions of ethanol. Ethanol inhibited specific [3H]nitrendipine binding with Ki = 460 mM, by decreasing binding affinity without altering the maximal number of sites labeled. At a lower concentration (100 mM), ethanol had no effect on inhibition of binding by verapamil or diltiazem. The high concentrations of ethanol required to produce alterations in [3H]nitrendipine binding suggest that ethanol and classical calcium channel antagonists influence calcium-mediated synaptic processes by separate mechanisms.
我们研究了乙醇对[3H]尼群地平与大鼠脑膜结合的影响,以探讨电压依赖性钙通道是否参与乙醇的突触作用。乙醇通过降低结合亲和力而不改变标记位点的最大数量,抑制特异性[3H]尼群地平结合,其Ki = 460 mM。在较低浓度(100 mM)时,乙醇对维拉帕米或地尔硫卓抑制结合没有影响。产生[3H]尼群地平结合改变所需的高浓度乙醇表明,乙醇和经典钙通道拮抗剂通过不同机制影响钙介导的突触过程。