Satayavivad J, Wongsawatkul O, Bunnag D, Tan-ariya P, Brockelman C R
Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Southeast Asian J Trop Med Public Health. 1987 Jun;18(2):253-8.
Using pharmacological properties in relation to the biochemistry of P. falciparum, verapamil, flunarizine, and chlorpromazine which are calcium blockers were selected to test for their antimalarial activity against P. falciparum in vitro. Results revealed that the drugs inhibited parasite population growth in the following order of IC50: verapamil 1 X 10(-6) M, chlorpromazine 3.5 X 10(-6) M, and flunarizine 5 X 10(-6) M. These three calcium blockers have antimalarial effects on chloroquine resistant parasite (alone T9/94) but are less potent when compared with the efficacy of quinine or mefloquine in vitro.
利用与恶性疟原虫生物化学相关的药理特性,选择钙阻滞剂维拉帕米、氟桂利嗪和氯丙嗪,在体外测试它们对恶性疟原虫的抗疟活性。结果显示,这些药物抑制寄生虫群体生长的IC50顺序如下:维拉帕米1×10(-6)M、氯丙嗪3.5×10(-6)M和氟桂利嗪5×10(-6)M。这三种钙阻滞剂对氯喹抗性寄生虫(单独的T9/94)有抗疟作用,但与奎宁或甲氟喹在体外的疗效相比,效力较低。