Hui K P, Ventresca P, Brown A C, Barnes P J, Chung K F
Department of Thoracic Medicine, National Heart & Lung Institute, Royal Brompton National Heart & Lung Hospital, London, UK.
Agents Actions. 1992 May;36(1-2):29-32. doi: 10.1007/BF01991224.
The effect of two beta 2-adrenoceptor agonists, salbutamol (100 micrograms/kg i.v.) and broxaterol (100 micrograms/kg i.v.), on airway microvascular leakage induced by vagal stimulation was studied in anaesthetised guinea pigs. Airway microvascular leakage was measured by Evans blue extravasation. Broxaterol, but not salbutamol, inhibited Evans blue dye extravasation at all airway levels, an effect prevented by pretreatment with propranolol (1 mg/kg). Neither of the beta 2-agonists had any effect on substance P-induced Evans blue dye extravasation. Broxaterol inhibits the prejunctional release of tachykinins from airway sensory nerves by stimulation of beta-receptors. The mechanism by which beta-adrenoceptor agonists prevent airway microvascular leakage deserves further study.
在麻醉的豚鼠中研究了两种β2肾上腺素能激动剂沙丁胺醇(静脉注射100微克/千克)和布地奈德(静脉注射100微克/千克)对迷走神经刺激诱导的气道微血管渗漏的影响。通过伊文思蓝外渗来测量气道微血管渗漏。布地奈德而非沙丁胺醇在所有气道水平均抑制伊文思蓝染料外渗,普萘洛尔(1毫克/千克)预处理可阻止该效应。两种β2激动剂对P物质诱导的伊文思蓝染料外渗均无影响。布地奈德通过刺激β受体抑制气道感觉神经中速激肽的节前释放。β肾上腺素能激动剂预防气道微血管渗漏的机制值得进一步研究。