Ozaki H, Shibata S, Kitano H, Matsumoto P, Ishida Y
Blood Vessels. 1981;18(6):321-9. doi: 10.1159/000158365.
Relaxing effects of nitroprusside and verapamil on the resting or K-stimulated tension and 45Ca uptake in human umbilical vessels were investigated. Both nitroprusside and verapamil reduced the resting and K-stimulated tensions in a dose-dependent manner. Nitroprusside was much more effective than verapamil in reducing resting tension. However, verapamil caused a greater relaxation of the K-induced contraction than nitroprusside. In a Ca2+-free medium, K+ still caused a small and sustained contraction. Nitroprusside abolished the contraction in the Ca2+-free medium, which verapamil failed to inhibit. Neither nitroprusside nor verapamil affected the resting 45Ca uptake measured by a lanthanum method. The K-induced increase in 45Ca uptake was inhibited by verapamil, but not by nitroprusside. The results suggest that nitroprusside unlike verapamil does not act as a Ca2+ influx inhibitor resulting in the relaxation of human umbilical vessels.
研究了硝普钠和维拉帕米对人脐血管静息或钾刺激张力及45钙摄取的舒张作用。硝普钠和维拉帕米均以剂量依赖方式降低静息和钾刺激张力。硝普钠在降低静息张力方面比维拉帕米有效得多。然而,维拉帕米比硝普钠能更有效地舒张钾诱导的收缩。在无钙培养基中,钾仍引起小而持续的收缩。硝普钠消除了无钙培养基中的收缩,而维拉帕米未能抑制。硝普钠和维拉帕米均不影响用镧法测定的静息45钙摄取。维拉帕米抑制钾诱导的45钙摄取增加,但硝普钠无此作用。结果表明,与维拉帕米不同,硝普钠不作为钙内流抑制剂导致人脐血管舒张。