Shimamoto H, Bourreau J P, Kwan C Y, Daniel E E
Department of Biomedical Sciences, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
J Pharmacol Exp Ther. 1992 Mar;260(3):1119-27.
The interactions between UK-14304 and other vasoconstrictor agents were investigated using isolated canine mesenteric vascular rings mounted in tissue baths for the measurement of isometric contraction. In the mesenteric artery, exposure to UK-14304 caused a small contraction, producing 8% of the KCl maximal response. In the presence of either 20 mM KCl or 10(-9) M endothelin-1, which had small contractile effects, UK-14304 produced a biphasic concentration-response curve; 10(-7) M rauwolscine inhibited the responses to low concentrations of UK-14304 and 10(-7) M prazosin blocked the responses to high concentrations of UK-14304. In the presence of 10(-8) M Bay K 8644, UK-14304 elicited a monophasic concentration-dependent contraction that was antagonized by 10(-7) M prazosin, not by 10(-7) M rauwolscine. In the mesenteric vein, UK-14304 elicited concentration-dependent contractions, producing 63% of the KCl maximal response. The lower part of the biphasic concentration-response curve was inhibited by 10(-7) M rauwolscine and the upper part of the curve was antagonized by 10(-7) M prazosin. The presence in the medium of 20 mM KCl, 10(-11) M endothelin-1 or 10(-9) M Bay K 8644, which increased resting tension less than 10% of the KCl maximal response, markedly enhanced the responses to UK-14304 primarily at concentrations lower than 10(-6) M. The enhancement of responses were prazosin (10(-7) M)-resistant and rauwolscine (10(-7) M)-sensitive.(ABSTRACT TRUNCATED AT 250 WORDS)
使用安装在组织浴槽中的离体犬肠系膜血管环来测量等长收缩,以此研究UK - 14304与其他血管收缩剂之间的相互作用。在肠系膜动脉中,暴露于UK - 14304会引起轻微收缩,产生的收缩幅度为氯化钾最大反应的8%。在存在20 mM氯化钾或10(-9) M内皮素 - 1(二者收缩作用轻微)的情况下,UK - 14304产生双相浓度 - 反应曲线;10(-7) M萝芙木碱抑制对低浓度UK - 14304的反应,而10(-7) M哌唑嗪阻断对高浓度UK - 14304的反应。在存在10(-8) M Bay K 8644的情况下,UK - 14304引发单相浓度依赖性收缩,该收缩被10(-7) M哌唑嗪拮抗,而非被10(-7) M萝芙木碱拮抗。在肠系膜静脉中,UK - 14304引发浓度依赖性收缩,产生的收缩幅度为氯化钾最大反应的63%。双相浓度 - 反应曲线的下部被10(-7) M萝芙木碱抑制,曲线的上部被10(-7) M哌唑嗪拮抗。培养基中存在20 mM氯化钾、10(-11) M内皮素 - 1或10(-9) M Bay K 8644(它们使静息张力增加幅度小于氯化钾最大反应的10%)时,主要在浓度低于10(-6) M时显著增强对UK - 14304的反应。反应增强对哌唑嗪(10(-7) M)有抗性,对萝芙木碱(10(-7) M)敏感。(摘要截取自250字)