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DuP 753和EXP3174对猫肺血管床中血管紧张素II反应的抑制作用。

Inhibitory effects of DuP 753 and EXP3174 on responses to angiotensin II in pulmonary vascular bed of the cat.

作者信息

McMahon T J, Kaye A D, Hood J S, Minkes R K, Nossaman B D, Kadowitz P J

机构信息

Department of Pharmacology, Tulane University School of Medicine, New Orleans, Louisiana 70112.

出版信息

J Appl Physiol (1985). 1992 Nov;73(5):2054-61. doi: 10.1152/jappl.1992.73.5.2054.

DOI:10.1152/jappl.1992.73.5.2054
PMID:1474085
Abstract

The effects of the non-peptide antagonist DuP 753 and its metabolite EXP3174 on responses to angiotensin II were investigated in the pulmonary vascular bed of the intact-chest cat. Under conditions of controlled blood flow and constant left atrial pressure, injections of angiotensin II into the perfused lobar artery caused dose-related increases in lobar arterial pressure. Responses to angiotensin II were reproducible and were not changed by meclofenamate or prazosin, indicating that prostaglandin or norepinephrine release does not mediate or modulate pulmonary vascular responses to the peptide. DuP 753 (1-5 mg/kg iv) decreased responses to angiotensin II in a competitive manner, and the duration of the blockade was related to dose of the antagonist. DuP 753 had no significant effect on responses to U-46619, norepinephrine, serotonin, endothelin-1, vasopressin, or BAY K 8644. EXP3174 also decreased responses to angiotensin II without altering responses to agents that act by a variety of mechanisms. The inhibitory effect of EXP3174 (1 mg/kg iv) was not overcome by angiotensin II in the range of doses studied, and the shift to the right of the dose-response curve was nonparallel, suggesting that the blockade was noncompetitive. The blockade was long in duration, and, when the dose of EXP3174 was decreased to 0.1 mg/kg iv, the blockade was surmounted and the shift to the right of the dose-response relationship was parallel. DuP 753 and EXP3174 had little effect on mean baseline pressures in the cat.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在开胸猫的肺血管床中研究了非肽拮抗剂杜普753(DuP 753)及其代谢产物EXP3174对血管紧张素II反应的影响。在控制血流和恒定左心房压力的条件下,向灌注的叶动脉注射血管紧张素II可引起叶动脉压力的剂量相关增加。对血管紧张素II的反应具有可重复性,且不受甲氯芬那酸或哌唑嗪的影响,这表明前列腺素或去甲肾上腺素的释放不介导或调节肺血管对该肽的反应。静脉注射杜普753(1 - 5毫克/千克)以竞争性方式降低对血管紧张素II的反应,且阻断持续时间与拮抗剂剂量有关。杜普753对U - 46619、去甲肾上腺素、5 - 羟色胺、内皮素 - 1、血管加压素或BAY K 8644的反应无显著影响。EXP3174也降低对血管紧张素II的反应,而不改变通过多种机制起作用的药物的反应。在所研究的剂量范围内,血管紧张素II不能克服EXP3174(静脉注射1毫克/千克)的抑制作用,且剂量反应曲线向右移位不平行,提示该阻断为非竞争性。阻断持续时间长,当EXP3174剂量降至静脉注射0.1毫克/千克时,阻断作用被克服,剂量反应关系向右的移位呈平行。杜普753和EXP3174对猫的平均基线压力影响很小。(摘要截短于250字)

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