Cesano L, Vietti Ramus G, Barbalonga A
Minerva Med. 1985 Sep 15;76(34-35):1549-52.
Verapamil in cultures of mammary carcinoma MCF7 cells and Jurkat A.L.L. cells decreased the 3H-TdR incorporation. The action of Verapamil is dose-dependent. The inhibition percentage of 3H-TdR incorporation into Jurkat cells by Verapamil was lower than into MCF7 cells. No change of the mitotic inhibition was observed with higher Ca++ concentration in the medium. Modification of the Na++ and K++ content in the medium did not change action of Verapamil; this is in agreement with the independence of neoplastic cells from the culture medium. Our investigation suggests that Verapamil does not work through a block of transmembrane Ca++ flux, but rather through an intracellular interaction.
维拉帕米作用于乳腺癌MCF7细胞和Jurkat A.L.L.细胞培养物时,会降低3H-胸腺嘧啶核苷(3H-TdR)的掺入量。维拉帕米的作用具有剂量依赖性。维拉帕米对Jurkat细胞3H-TdR掺入的抑制百分比低于对MCF7细胞的抑制百分比。培养基中较高的钙离子(Ca++)浓度未观察到有丝分裂抑制的变化。培养基中钠离子(Na++)和钾离子(K++)含量的改变并未改变维拉帕米的作用;这与肿瘤细胞对培养基的独立性相符。我们的研究表明,维拉帕米并非通过阻断跨膜Ca++通量起作用,而是通过细胞内相互作用发挥作用。