Lee S L, Long K, Ueda S, Fanburg B L
J Cell Physiol. 1987 Jul;132(1):178-82. doi: 10.1002/jcp.1041320126.
Verapamil inhibited Na+-dependent uptake of serotonin (5-HT) by bovine pulmonary artery endothelial cells in culture both exposed to room air and stimulated by prior exposure to anoxia. The effect of verapamil occurred even in the absence of Ca2+ from the assay medium. Although absence of Ca2+ from the medium moderately reduced 5-HT uptake, stimulation of uptake was nevertheless observed for cells previously exposed to anoxia. Verapamil altered the Km, but not the Vmax, of 5-HT uptake. There was no change in 45Ca2+ uptake or release by cells previously exposed to anoxia as compared to those exposed to room air and verapamil did not influence 45Ca2+ fluxes by either set of cells. It is concluded that verapamil inhibits 5-HT uptake by endothelial cells through a mechanism other than Ca2+ channel blockade; the results are consistent with competitive inhibition of a 5-HT carrier. The stimulatory effect of anoxia on 5-HT uptake does not occur through a change in Ca2+ fluxes.
维拉帕米抑制培养的牛肺动脉内皮细胞对5-羟色胺(5-HT)的钠依赖性摄取,这些细胞既暴露于室内空气,又因先前暴露于缺氧环境而受到刺激。即使在测定培养基中不存在Ca2+的情况下,维拉帕米的作用依然出现。尽管培养基中不存在Ca2+会适度降低5-HT摄取,但对于先前暴露于缺氧环境的细胞,仍观察到摄取的刺激作用。维拉帕米改变了5-HT摄取的米氏常数(Km),但未改变最大反应速度(Vmax)。与暴露于室内空气的细胞相比,先前暴露于缺氧环境的细胞对45Ca2+的摄取或释放没有变化,并且维拉帕米对这两组细胞的45Ca2+通量均无影响。得出的结论是,维拉帕米通过一种不同于Ca2+通道阻断的机制抑制内皮细胞对5-HT的摄取;结果与对5-HT载体的竞争性抑制一致。缺氧对5-HT摄取的刺激作用并非通过Ca2+通量的改变而发生。