Kannan M S, Davis C
Department of Veterinary Biology, College of Veterinary Medicine, University of Minnesota, St. Paul 55108.
Respir Physiol. 1988 Oct;74(1):15-23. doi: 10.1016/0034-5687(88)90136-3.
Calcium antagonists have been shown to inhibit exercise-induced asthma. The mechanism of inhibition is unclear, but may involve inhibition of mediator release and/or blockade of the mediator effects. We studied the effects of methoxyverapamil (D600) on human airway responses to spasmogens as well as on histamine release from passively sensitized human lung challenged with ragweed antigen. The concentrations of D600 required to inhibit 50% of the spasmogen responses (IC50) were calculated from the concentration-response relationships and were: histamine 4 x 10(-6) M; KCl 7 x 10(-7) M; leukotriene C4 4 x 10(-5) M; electrical field stimulation 5 x 10(-5) M; and for ragweed antigen in passively sensitized muscle 2 x 10(-6) M. Histamine release by antigen challenge from sensitized lung fragments was not blocked by D600, up to a concentration of 10(-5) M. The data suggest that the contractile effects of agonists are mediated through voltage- and receptor-operated calcium channels. The differential inhibitory effects of D600 on antigen-induced mediator release vs the smooth muscle effects of the various agonists may suggest multiple mechanisms of release or sources of mediators in human airway anaphylaxis.
钙拮抗剂已被证明可抑制运动诱发的哮喘。其抑制机制尚不清楚,但可能涉及抑制介质释放和/或阻断介质的作用。我们研究了甲氧基维拉帕米(D600)对人气道对致痉剂的反应以及对豚草抗原激发的被动致敏人肺组织中组胺释放的影响。根据浓度-反应关系计算出抑制50%致痉剂反应所需的D600浓度(IC50),结果如下:组胺4×10⁻⁶ M;氯化钾7×10⁻⁷ M;白三烯C4 4×10⁻⁵ M;电场刺激5×10⁻⁵ M;对于被动致敏肌肉中的豚草抗原为2×10⁻⁶ M。在浓度高达¹⁰⁻⁵ M时,D600并未阻断抗原激发致敏肺组织片段释放组胺。数据表明,激动剂的收缩作用是通过电压门控和受体操纵的钙通道介导的。D600对抗原诱导的介质释放与各种激动剂对平滑肌的作用具有不同的抑制作用,这可能提示人气道过敏反应中介质释放或介质来源的多种机制。