DePietro F R, Byrd J C
Department of Psychiatry, University of Pittsburgh, Pennsylvania.
J Mol Neurosci. 1990;2(1):45-52. doi: 10.1007/BF02896925.
Phencyclidine (PCP) binds with high affinity to the ion channel associated with the NMDA receptor. The binding of the PCP receptor-specific ligand TCP is greatly reduced at temperatures between 2 degrees C and 6 degrees C, at which the plasma membrane is in a rigid state. However, membrane rigidity alone does not appear to cause the reduced TCP binding, since the membrane fluidizing agent A2C did not increase TCP binding at 4 degrees C; instead, it decreased binding at 21 degrees C. This inhibitory effect of A2C on TCP binding was dose dependent and was highly correlated with A2C-induced increases in membrane fluidity. The IC50 of A2C inhibition was 8.9 mM, with a pseudo-Hill coefficient of -0.24. Scatchard analysis demonstrated that this effect was the result of an increase in the apparent KD of [3H]TCP for the PCP receptor, with no effect on the Bmax. These results suggest that the function of the NMDA-PCP receptor complex is impaired by increases in membrane fluidity. These findings may be pharmacologically relevant in understanding the mechanism of action of such agents as general anesthetics and ethanol, which cause increases in plasma membrane fluidity.
苯环己哌啶(PCP)与与N-甲基-D-天冬氨酸(NMDA)受体相关的离子通道具有高亲和力结合。PCP受体特异性配体TCP的结合在2摄氏度至6摄氏度之间的温度下大幅降低,此时质膜处于刚性状态。然而,单独的膜刚性似乎并不会导致TCP结合减少,因为膜流化剂A2C在4摄氏度时并未增加TCP结合;相反,它在21摄氏度时降低了结合。A2C对TCP结合的这种抑制作用是剂量依赖性的,并且与A2C诱导的膜流动性增加高度相关。A2C抑制的半数抑制浓度(IC50)为8.9毫摩尔,假希尔系数为-0.24。斯卡查德分析表明,这种效应是[3H]TCP对PCP受体的表观解离常数(KD)增加的结果,而对最大结合容量(Bmax)没有影响。这些结果表明,膜流动性增加会损害NMDA-PCP受体复合物的功能。这些发现可能在药理学上与理解全身麻醉剂和乙醇等药物的作用机制相关,这些药物会导致质膜流动性增加。