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豚鼠离体气管中所选收缩激动剂的功能相互作用分析

An analysis of the functional interactions of selected contractile agonists in the guinea pig isolated trachea.

作者信息

Undem B J, Adams G K

机构信息

Johns Hopkins University School of Medicine, Good Samaritan Hospital, Baltimore, Maryland.

出版信息

J Pharmacol Exp Ther. 1988 Jul;246(1):47-53.

PMID:2839671
Abstract

Functional interactions between several contractile agonists were examined in the guinea pig isolated trachea. Cumulative concentration-response effects of agonist A were obtained in the absence and presence of steady-state contractions induced by agonist B. The agonists examined included histamine, prostaglandin D2, platelet activating factor, leukotrienes E4 and D4 and carbamylcholine. We found that none of the agonists studied caused a leftward shift in the concentration-response curve of a second agonist, nor did any agonist decrease the concentration of a second agonist required to evoke a maximum response. In general the functional interactions fit the predictions based on the early models of functional additivity. However, the interactions deviated categorically from this model in that there was less than predicted additivity at concentrations of the interactants that alone induced greater than a 50% response. The degree to which this deviation occurred was agonist dependent. The results suggest that in the guinea pig trachea a contractile agonist does not uncover or increase a reserve in the receptor-subeffect-response chain of a second contractile agonist. The findings that the quantitative nature of the interactions were somewhat agonist dependent supports the hypothesis that more than one biochemical mechanism is involved in the receptor-mediated contraction of airway smooth muscle.

摘要

在豚鼠离体气管中研究了几种收缩激动剂之间的功能相互作用。在不存在和存在由激动剂B诱导的稳态收缩的情况下,获得了激动剂A的累积浓度-反应效应。所研究的激动剂包括组胺、前列腺素D2、血小板活化因子、白三烯E4和D4以及氨甲酰胆碱。我们发现,所研究的激动剂均未导致第二种激动剂的浓度-反应曲线向左移动,也没有任何激动剂降低引发最大反应所需的第二种激动剂的浓度。一般来说,功能相互作用符合基于早期功能相加模型的预测。然而,这些相互作用与该模型有明显偏差,因为在单独诱导大于50%反应的相互作用剂浓度下,相加性低于预测值。这种偏差发生的程度取决于激动剂。结果表明,在豚鼠气管中,一种收缩激动剂不会揭示或增加第二种收缩激动剂的受体-亚效应-反应链中的储备。相互作用的定量性质在一定程度上取决于激动剂这一发现支持了这样的假设,即气道平滑肌受体介导的收缩涉及不止一种生化机制。

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