Suppr超能文献

渥曼青霉素对主动致敏的棕色挪威大鼠支气管收缩反应中腺苷作用的影响。

Effects of wortmannin on bronchoconstrictor responses to adenosine in actively sensitised Brown Norway rats.

作者信息

Tigani B, Hannon J P, Mazzoni L, Fozard J R

机构信息

Research Department, Novartis Pharma AG, 4002, Basel, Switzerland.

出版信息

Eur J Pharmacol. 2000 Oct 20;406(3):469-76. doi: 10.1016/s0014-2999(00)00705-6.

Abstract

The bronchoconstrictor response to adenosine in the actively sensitised Brown Norway rat is markedly augmented following low level allergen (ovalbumin) challenge. The response reflects activation of the A(2B) receptor subtype and is mediated by 5-hydroxytryptamine (5-HT) released as a consequence of mast cell activation. We describe here the effects of wortmannin, a potent inhibitor of phosphatidylinositol-3-kinase and mast cell exocytosis, on the response to adenosine. Bronchoconstrictor responses to adenosine elicited 3 h following ovalbumin challenge were markedly and dose-dependently reduced by wortmannin given intratracheally (i. t.), 1 h prior to or 2 h post-allergen challenge. Responses to methacholine, which activates bronchial smooth muscle directly, and 5-HT were also reduced following wortmannin but to a lesser extent than those to adenosine. Bronchoconstrictor responses to adenosine 3 h post-challenge with vehicle were also markedly reduced by wortmannin given intratracheally (i.t.), 1 h prior to the "sham" challenge. Plasma histamine and 5-HT levels increased in response to adenosine given 3 h following ovalbumin challenge. The increases were suppressed by wortmannin given i.t., 2 h post-ovalbumin challenge. A reduction in the sensitivity of the airways to 5-HT explains in part the reduced bronchoconstrictor response to adenosine induced by wortmannin. A direct action to suppress 5-HT release from airway mast cells induced by adenosine also contributes to the reduction in the response. Inhibition of phosphatidylinositol-3-kinase is the presumed mechanistic basis for the observed effects.

摘要

在低水平变应原(卵清蛋白)激发后,主动致敏的棕色挪威大鼠对腺苷的支气管收缩反应显著增强。该反应反映了A(2B)受体亚型的激活,并且由肥大细胞激活后释放的5-羟色胺(5-HT)介导。我们在此描述渥曼青霉素(一种磷脂酰肌醇-3-激酶和肥大细胞胞吐作用的强效抑制剂)对腺苷反应的影响。在卵清蛋白激发前1小时或激发后2小时经气管内(i.t.)给予渥曼青霉素,可显著且剂量依赖性地降低卵清蛋白激发3小时后引发的对腺苷的支气管收缩反应。对直接激活支气管平滑肌的乙酰甲胆碱和5-HT的反应在渥曼青霉素处理后也有所降低,但程度小于对腺苷的反应。在“假”激发前1小时经气管内(i.t.)给予渥曼青霉素,也可显著降低用赋形剂激发3小时后对腺苷的支气管收缩反应。卵清蛋白激发3小时后给予腺苷会使血浆组胺和5-HT水平升高。卵清蛋白激发后2小时经气管内(i.t.)给予渥曼青霉素可抑制这种升高。气道对5-HT敏感性的降低部分解释了渥曼青霉素诱导的对腺苷的支气管收缩反应减弱。直接抑制腺苷诱导的气道肥大细胞释放5-HT也有助于反应的减弱。磷脂酰肌醇-3-激酶的抑制是观察到的这些效应的推测机制基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验