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白三烯D4和前列腺素F2α诱导豚鼠气流阻塞和气道血浆渗出:血栓素及其受体的作用

Leukotriene D4- and prostaglandin F2 alpha-induced airflow obstruction and airway plasma exudation in guinea-pig: role of thromboxane and its receptor.

作者信息

Arakawa H, Lötvall J, Kawikova I, Löfdahl C G, Skoogh B E

机构信息

Division of Clinical Pharmacology (Department of Pharmacology), Göteborg University, Sweden.

出版信息

Br J Pharmacol. 1993 Sep;110(1):127-32. doi: 10.1111/j.1476-5381.1993.tb13781.x.

DOI:10.1111/j.1476-5381.1993.tb13781.x
PMID:8220872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2176029/
Abstract
  1. We studied the effects of a thromboxane A2 receptor (TP receptor) antagonist, ICI-192,605 (0.5 mg kg-1, i.v.) and a selective thromboxane (Tx) synthetase inhibitor, OKY-046 (30 mg kg-1, i.v.), on airway responses induced by leukotriene D4 (LTD4; 0.2 nmol) or prostaglandin F2 alpha (PGF2 alpha; 20 nmol) instilled via the airways route to anaesthetized guinea-pigs. For a comparison, airway responses to a TxA2-mimetic, U-46619 (0.02 nmol) were also studied. We measured both lung resistance (RL) to monitor airflow obstruction, and extravasation of Evans Blue dye to quantify airway plasma exudation. 2. Instilled LTD4 into the tracheal lumen induced an immediate peak and subsequently persistent increase in RL and produced a large amount of extravasation of Evans Blue dye at all airway levels. Both ICI-192,605 and OKY-046 significantly attenuated the persistent increase in RL following the immediate response and reduced LTD4-induced extravasation of Evans Blue dye in the trachea and proximal intrapulmonary airway. Instilled LTD4 produced significant increases in immunoreactive TxB2 in bronchoalveolar lavage fluid obtained 1.5 min after instillation of LTD4. 3. Instilled PGF2 alpha into the tracheal lumen induced an immediate increase in RL which peaked at approximately 15 s. We also observed a delayed sustained increase in RL, reaching a second peak at approximately 4 min. PGF2 alpha produced small but significant increases in the amount of Evans Blue dye at all airway levels. As with PGF2 alpha, instillation of U-46619 produced a biphasic increase in RL and extravasation of Evans Blue dye. The potency of PGF2a, in inducing these airway responses was about 1000 times less than U-46619. ICI-192,605 abolished both the immediate and the delayed increase in RL after PGF2a, and also blocked PGF2a,-induced extravasation of Evans Blue dye. However, OKY-046 had no inhibitory effects on these responses.4. We conclude that airflow obstruction and airway plasma exudation induced by instilled LTD4 is, in part, mediated via TxA2 generation and subsequent activation of TP-receptors. On the other hand,instilled PGF2a, while inducing similar responses, does so primarily by direct activation of TP receptors,rather than via TxA2 generation.
摘要
  1. 我们研究了血栓素A2受体(TP受体)拮抗剂ICI-192,605(0.5毫克/千克,静脉注射)和选择性血栓素(Tx)合成酶抑制剂OKY-046(30毫克/千克,静脉注射)对通过气道途径向麻醉豚鼠气道内滴注白三烯D4(LTD4;0.2纳摩尔)或前列腺素F2α(PGF2α;20纳摩尔)所诱导的气道反应的影响。为作比较,还研究了气道对TxA2模拟物U-46619(0.02纳摩尔)的反应。我们测量了肺阻力(RL)以监测气流阻塞情况,并测量伊文思蓝染料的渗出量以量化气道血浆渗出情况。2. 向气管腔内滴注LTD4可立即引起RL峰值,随后持续升高,并在所有气道水平均导致大量伊文思蓝染料渗出。ICI-192,605和OKY-046均能显著减轻即刻反应后RL的持续升高,并减少LTD4诱导的气管和肺内近端气道伊文思蓝染料的渗出。滴注LTD4后1.5分钟获得的支气管肺泡灌洗液中免疫反应性TxB2显著增加。3. 向气管腔内滴注PGF2α可立即引起RL升高,约15秒时达到峰值。我们还观察到RL有延迟的持续升高,约4分钟时达到第二个峰值。PGF2α在所有气道水平均使伊文思蓝染料渗出量有少量但显著的增加。与PGF2α一样,滴注U-46619也使RL和伊文思蓝染料渗出呈双相增加。PGF2α诱导这些气道反应的效力比U-46619约低1000倍。ICI-192,605消除了PGF2α后RL的即刻和延迟升高,也阻断了PGF2α诱导的伊文思蓝染料渗出。然而,OKY-046对这些反应无抑制作用。4. 我们得出结论,滴注LTD4所诱导的气流阻塞和气道血浆渗出部分是通过TxA2生成及随后TP受体的激活介导的。另一方面,滴注PGF2α虽然诱导类似反应,但其主要是通过直接激活TP受体,而非通过TxA2生成来实现的。

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Nanomolar concentrations of prostaglandin F2 alpha potentiate cholinergic contractions of rabbit isolated tracheal muscle.纳摩尔浓度的前列腺素F2α可增强兔离体气管肌肉的胆碱能收缩。
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