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花生四烯酸代谢抑制剂对猪离体气管平滑肌药物诱导收缩的影响。

The effect of inhibitors of arachidonic acid metabolism on drug-induced contractions in isolated tracheal smooth muscle of the pig.

作者信息

Mitchell H W

出版信息

Br J Pharmacol. 1982 Jan;75(1):129-36. doi: 10.1111/j.1476-5381.1982.tb08765.x.

Abstract

1 The regulation of drug-induced tone in airways smooth muscle was examined in an isolated preparation of swine tracheal smooth muscle. 2 The trachea contracted (isometric) to histamine, 2-pyridylethylamine (2-PEA), acetylcholine and K+ but no response to histamine H2-receptor agonists were observed. 3 Histamine-induced contractions (100 microM) were potentiated by 213.3% by indomethacin (1 microM) and by 126.9% by sodium salicylate (250 microM). These inhibitors had only slight or no effects on acetylcholine-induced tone. 2-PEA responses were also potentiated by indomethacin but there were no changes in the response to H2-receptor agonists in the presence of indomethacin. The indomethacin-mediated potentiation of histamine was blocked by 5, 8, 11, 14-eicosatetraynoic acid (10 microM). FPL 55712 had no effect on these responses. 4 Mepacrine (100 microM) inhibited responses to histamine but not those to acetylcholine. No effect was observed with dexamethasone (up to 100 microM). 5 Prostaglandin E2 caused relaxation but arachidonic acid did not. 6 The possibility that histamine H1-agonist-induced contractions are regulated by contractile products of the arachidonic acid lipoxygenase pathway is discussed.

摘要

1 在猪气管平滑肌的离体标本中研究了气道平滑肌中药物诱导张力的调节。2 气管对组胺、2-吡啶乙胺(2-PEA)、乙酰胆碱和K+产生收缩(等长收缩),但未观察到对组胺H2受体激动剂的反应。3 吲哚美辛(1 μM)使组胺诱导的收缩(100 μM)增强213.3%,水杨酸钠(250 μM)使其增强126.9%。这些抑制剂对乙酰胆碱诱导的张力只有轻微影响或无影响。吲哚美辛也增强了2-PEA的反应,但在吲哚美辛存在下,对H2受体激动剂的反应没有变化。吲哚美辛介导的组胺增强作用被5,8,11,14-二十碳四烯酸(10 μM)阻断。FPL 55712对这些反应无影响。4 甲氯喹啉(100 μM)抑制对组胺的反应,但不抑制对乙酰胆碱的反应。地塞米松(高达100 μM)未观察到影响。5 前列腺素E2引起舒张,但花生四烯酸没有。6 讨论了组胺H1激动剂诱导的收缩是否受花生四烯酸脂氧合酶途径收缩产物调节的可能性。

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