Manzini S, Maggi C A, Meli A
J Pharmacol Methods. 1982 Aug;8(1):47-57. doi: 10.1016/0160-5402(82)90007-9.
Although the response of vascular smooth muscle to norepinephrine (NE) is biphasic in nature, there is no simple procedure for the separate quantitative analysis of intracellular and extracellular Ca++ dependent NE-induced contractions. Intraluminal NE in high-K+Ca++-free medium produces a dose-dependent contraction which is selectively antagonized by procaine (1 X 10(-3) M--5 X 10(-3) M). Subsequent reperfusion with normal Krebs of NE-pretreated arterial segments results in a dose-dependent contraction which is strictly related to extracellular Ca++ concentration and is selectively inhibited by verapamil (5 X 10(-6) M--5 X 10(-5) M). These results can be interpreted as an indication that this procedure is suitable for the separate analysis of the capability of vasoactive drugs to differentially mobilize cellular and extracellular Ca++ pools in perfused rabbit ear artery preparations.
尽管血管平滑肌对去甲肾上腺素(NE)的反应本质上是双相的,但对于细胞内和细胞外Ca++依赖性NE诱导的收缩进行单独定量分析,尚无简单的方法。在高钾无钙培养基中的腔内NE产生剂量依赖性收缩,可被普鲁卡因(1×10(-3)M - 5×10(-3)M)选择性拮抗。随后用正常的Krebs液对NE预处理的动脉段进行再灌注,会产生剂量依赖性收缩,这与细胞外Ca++浓度密切相关,并被维拉帕米(5×10(-6)M - 5×10(-5)M)选择性抑制。这些结果可以解释为,该方法适用于在灌注兔耳动脉制剂中,对血管活性药物差异性动员细胞内和细胞外Ca++池的能力进行单独分析。