Fletcher E J, Church J, MacDonald J F
Department of Physiology, University of Toronto, Ont., Canada.
Eur J Pharmacol. 1994 Apr 15;267(2):249-52. doi: 10.1016/0922-4106(94)90178-3.
The Ca2+ channel antagonist action of the antipsychotic haloperidol was investigated using two functional assays of Ca2+ channel activity. Haloperidol dose dependently attenuated the rise in intracellular free Ca2+ ([Ca2+]i) evoked by 50 mM extracellular K+ in Fura-2 loaded cultured rat hippocampal neurones with an IC50 (+/- S.E.M.) of 7.8 +/- 0.5 microM and similarly reduced whole-cell Ba2+ currents (IBa) in voltage-clamped mouse hippocampal neurones with an IC50 value of 15.6 +/- 1.1 microM. Block of whole-cell IBa by haloperidol was rapid, fully reversible, and was greater at more depolarized membrane potentials. Our data indicate that haloperidol non-selectively blocks neuronal voltage-gated Ca2+ channels at micromolar concentrations.
利用两种钙离子通道活性功能测定方法,研究了抗精神病药物氟哌啶醇的钙离子通道拮抗作用。氟哌啶醇剂量依赖性地减弱了50 mM细胞外钾离子在Fura-2负载的培养大鼠海马神经元中诱发的细胞内游离钙离子浓度([Ca2+]i)升高,其半数抑制浓度(IC50,±标准误)为7.8±0.5 microM,同样地,在电压钳制的小鼠海马神经元中,氟哌啶醇也以15.6±1.1 microM的IC50值降低了全细胞钡离子电流(IBa)。氟哌啶醇对全细胞IBa的阻断迅速、完全可逆,且在膜电位去极化程度更高时作用更强。我们的数据表明,氟哌啶醇在微摩尔浓度下非选择性地阻断神经元电压门控钙离子通道。