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血栓素受体拮抗剂对前列腺素D2和组胺所致人体支气管收缩的影响。

Effects of a thromboxane receptor antagonist on prostaglandin D2 and histamine induced bronchoconstriction in man.

作者信息

al Jarad N, Hui K P, Barnes N

机构信息

Department of Thoracic Medicine, London Chest Hospital.

出版信息

Br J Clin Pharmacol. 1994 Jan;37(1):97-100. doi: 10.1111/j.1365-2125.1994.tb04249.x.

Abstract

Many prostanoids including are prostaglandin (PG) F2 alpha and PGD2 are potent bronchoconstrictor agents. There is evidence to suggest that airway thromboxane (TP) receptor may act as a common receptor for their bronchoconstrictor actions. We tested the hypothesis that inhaled prostaglandin (PG) D2-induced bronchoconstriction is mediated by interacting with the TP receptor antagonist, ICI 192605, on the bronchoconstrictor response to inhaled PGD2 in a double-blind, placebo-controlled and crossed-over trial in normal subjects. The effect of ICI 192605 on histamine induced bronchoconstriction served as control for non-specific bronchodilatory actions. The study had two phases; the first consisted of two inhaled PGD2 challenge study days, and the second phase was that of inhaled histamine. Each study day was separated by at least a week. On each study day, the challenge tests were carried out 30 min after ingestion of 100 mg ICI 192605 or placebo. Doubling concentrations of agonist were given till more than 35% fall in post-diluent specific airway conductance (sGaw) occurred. The concentration needed to cause a fall in a sGaw of 35% post-diluent value (PC35sGaw) was then determined from linear interpolation of the log dose-response. Eight male subjects (median age 26, range 20-35 years) completed the study. ICI 192605 did not change baseline airway calibre 30 min after ingestion on either PGD2 or histamine study days. ICI 192605 significantly shifted the dose-response curve to inhaled PGD2 to the right by a median of 3.4 fold (Wilcoxon rank sign test, P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

包括前列腺素(PG)F2α和PGD2在内的许多类前列腺素都是强效支气管收缩剂。有证据表明,气道血栓素(TP)受体可能是它们发挥支气管收缩作用的共同受体。我们在一项针对正常受试者的双盲、安慰剂对照和交叉试验中,检验了吸入前列腺素(PG)D2诱导的支气管收缩是通过与TP受体拮抗剂ICI 192605相互作用介导的这一假设,该拮抗剂作用于吸入PGD2后的支气管收缩反应。ICI 192605对组胺诱导的支气管收缩的作用作为非特异性支气管扩张作用的对照。该研究有两个阶段;第一阶段包括两个吸入PGD2激发研究日,第二阶段是吸入组胺。每个研究日至少间隔一周。在每个研究日,在摄入100毫克ICI 192605或安慰剂30分钟后进行激发试验。给予双倍浓度的激动剂,直到稀释后特定气道传导率(sGaw)下降超过35%。然后通过对数剂量反应的线性插值法确定导致稀释后sGaw下降35%(PC35sGaw)所需的浓度。八名男性受试者(中位年龄26岁,范围20 - 35岁)完成了该研究。在PGD2或组胺研究日,摄入ICI 192605 30分钟后,其并未改变基线气道口径。ICI 192605使吸入PGD2的剂量反应曲线显著右移,中位数为3.4倍(Wilcoxon秩和检验,P < 0.05)。(摘要截短于250字)

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