Snell L D, Jones S M, Johnson K M
Neurosci Lett. 1987 Aug 5;78(3):333-7. doi: 10.1016/0304-3940(87)90383-1.
This study examined the ability of phencyclidine (PCP) to inhibit the responses to N-methyl-D-aspartate (NMDA) in depolarizing concentrations of K+. The effects of PCP and Mg2+ on NMDA-induced norepinephrine release from hippocampal slices were measured during superfusion with various extracellular concentrations of K+. The IC50 values for Mg2+ and PCP were significantly higher in K+ concentrations above 6 mM. These data are supportive of the hypothesis that PCP produces a voltage-dependent blockade of NMDA-activated ion channels.
本研究检测了苯环己哌啶(PCP)在去极化浓度的钾离子(K⁺)中抑制对N-甲基-D-天冬氨酸(NMDA)反应的能力。在用不同细胞外浓度的K⁺进行灌流期间,测定了PCP和镁离子(Mg²⁺)对NMDA诱导的海马切片去甲肾上腺素释放的影响。在K⁺浓度高于6 mM时,Mg²⁺和PCP的半数抑制浓度(IC50)值显著更高。这些数据支持了以下假说:PCP对NMDA激活的离子通道产生电压依赖性阻断作用。