Torphy T J, Burman M, Schwartz L W, Wasserman M A
J Pharmacol Exp Ther. 1986 Apr;237(1):332-40.
The effects of leukotriene D4 and methacholine on cyclic nucleotide content and isoproterenol-induced relaxation were examined in the isolated opossum trachea. Although leukotriene D4 (-log EC50 = 6.70) was a more potent contractile agent than methacholine (-log EC50 = 5.78), the maximal response to leukotriene D4 was only 65% of the maximum response to methacholine. Contraction of tracheal strips with leukotriene D4 was accompanied by a 3-fold increase in cyclic GMP accumulation. Methacholine-induced contraction was not associated with an increase in cyclic GMP. Neither agent altered basal cyclic AMP content. Additional experiments were carried out to examine functional inhibitory interactions between bronchoconstricting and bronchodilating pathways. In these studies, cumulative isoproterenol concentration-response curves were constructed in tracheal strips contracted with three different concentrations of methacholine and in tissues contracted with three corresponding equieffective concentrations of leukotriene D4. Although the relaxant response to isoproterenol decreased as tissues were contracted with higher concentrations of either agent, the inhibitory effect of methacholine on isoproterenol-induced relaxation was much greater than the inhibitory effect of leukotriene D4. Previous studies from our laboratory suggested that a potential explanation for the greater inhibitory effect of methacholine on the mechanical response to isoproterenol was that methacholine may inhibit isoproterenol-stimulated cyclic AMP accumulation whereas leukotriene D4 may not. However, neither methacholine nor leukotriene D4 inhibited isoproterenol-stimulated cyclic AMP accumulation in the opossum trachea. The results of this study indicate that the sensitivity of airway smooth muscle to beta adrenoceptor agonists is influenced both by the initial contractile state of the tissue and by the type of agent used to induce tone.
在分离的负鼠气管中研究了白三烯D4和乙酰甲胆碱对环核苷酸含量及异丙肾上腺素诱导的舒张作用的影响。尽管白三烯D4(-log EC50 = 6.70)比乙酰甲胆碱(-log EC50 = 5.78)是更强效的收缩剂,但白三烯D4的最大反应仅为乙酰甲胆碱最大反应的65%。白三烯D4引起气管条收缩的同时,环鸟苷酸积累增加了3倍。乙酰甲胆碱诱导的收缩与环鸟苷酸增加无关。两种药物均未改变基础环磷酸腺苷含量。进行了额外实验以研究支气管收缩和舒张途径之间的功能抑制相互作用。在这些研究中,在分别用三种不同浓度的乙酰甲胆碱收缩的气管条以及用三种相应等效浓度的白三烯D4收缩的组织中构建了异丙肾上腺素累积浓度-反应曲线。尽管随着组织用更高浓度的任何一种药物收缩,对异丙肾上腺素的舒张反应降低,但乙酰甲胆碱对异丙肾上腺素诱导的舒张的抑制作用远大于白三烯D4的抑制作用。我们实验室先前的研究表明,乙酰甲胆碱对异丙肾上腺素机械反应具有更大抑制作用的一个潜在解释可能是乙酰甲胆碱可能抑制异丙肾上腺素刺激的环磷酸腺苷积累,而白三烯D4可能不会。然而,乙酰甲胆碱和白三烯D4均未抑制负鼠气管中异丙肾上腺素刺激的环磷酸腺苷积累。本研究结果表明,气道平滑肌对β肾上腺素能受体激动剂的敏感性受组织的初始收缩状态和用于诱导张力的药物类型的影响。