Siegl P K, Rossi G V, Orzechowski R F
Eur J Pharmacol. 1979 Feb 15;54(1-2):1-7. doi: 10.1016/0014-2999(79)90400-x.
Isolated lung strips of guinea pigs were examined as an in vitro model for assessing the direct effect of beta-adrenergic drugs at the level of peripheral airways. Changes in intrinsic tone of thin strips of lung parenchyma were measured with an isometric force transducer. Isoproterenol, a nonselective beta-adrenergic agonist, and several beta-adrenergic agonists, soterenol, salbutamol, metaproterenol and ritodrine elicited a dose-related relaxation of lung strip. Responses to isoproterenol were antagonized by propranolol and the selective beta blocking agents butoxamine (beta2) and practolol (beta1). These results were compared to data obtained with the same compounds on isolated guinea pig atria. All agonists except ritodrine were full agonists in the lung strip whereas isoproterenol and metaproterenol were the only full agonists in the atrial preparation. In the atria, practolol was a more effective blocker of isoproterenol responses than butoxamine, and the reverse was true for the lung strip.
将豚鼠的离体肺条作为体外模型,用于评估β-肾上腺素能药物在外周气道水平的直接作用。用等长力传感器测量肺实质细条的内在张力变化。异丙肾上腺素(一种非选择性β-肾上腺素能激动剂)以及几种β-肾上腺素能激动剂索特仑、沙丁胺醇、间羟异丙肾上腺素和利托君均可引起肺条剂量相关的舒张。普萘洛尔以及选择性β受体阻滞剂布托沙明(β2)和普拉洛尔(β1)可拮抗对异丙肾上腺素的反应。将这些结果与用相同化合物在豚鼠离体心房上获得的数据进行比较。除利托君外,所有激动剂在肺条中均为完全激动剂,而异丙肾上腺素和间羟异丙肾上腺素在心房标本中是仅有的完全激动剂。在心房中,普拉洛尔比布托沙明更有效地阻断异丙肾上腺素反应,而在肺条中情况则相反。