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维拉帕米通过一种与钙通道阻滞无关的机制抑制培养的内皮细胞摄取5-羟色胺。

Verapamil inhibits serotonin uptake of endothelial cells in culture by a mechanism unrelated to Ca2+ channel blockade.

作者信息

Lee S L, Long K, Ueda S, Fanburg B L

出版信息

J Cell Physiol. 1987 Jul;132(1):178-82. doi: 10.1002/jcp.1041320126.

Abstract

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.

摘要

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。

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