摘要
目的 观测新型的ATP敏感钾通道开放剂EMD56431(EMD) 的平喘作用,并与钙通道阻滞剂粉防己碱(tetrandrine,Tet)比较。方法 豚鼠离体气管法和整体药物引喘法。结果 EMD 能抑制KCl 所致豚鼠气管螺旋条的收缩反应,其抑制作用随[K+]o 浓度的增高而减弱;EMD 能浓度依赖性地使氨甲酰胆碱和组胺的量效曲线右移,最大效应降低,均表现为非竞争性拮抗,pD′2 值分别为4-45 和4-40 ;组胺喷雾引起的豚鼠哮喘模型中,EMD 灌胃能剂量依赖性地使豚鼠的引喘潜伏期延长,抽搐动物数亦随剂量增加而减少(n = 8 ,P< 0-05)。结论 EMD 的支气管扩张作用在于开放钾通道,其作用强于Tet,两者具有协同作用。EMD 单用或与Tet
AIM To elucidate the effects of EMD 56431 (EMD) on guinea pig airway smooth muscle and compare with tetrandrine (Tet). METHODS The methods of isolated guinea pig trachea and the whole animals asthma in conscious guinea pigs were used to observe antiasthmatic effect. RESULTS EMD inhibited KCl induced contraction in guinea pig isolated tracheal spirals. Its effect decreased while[K+]Oconcentrationsincreased.EMDcouldmarkedlyinhibitthecontractionoftrachealspiralsinducedbycarbacholandhistaminerespectivelyinaconcentrationdependentmanner,shiftedthecumulativedoseresponsecurvesofcarbacholandhistaminetoright,andreducedthemaximalefficacyofcontractioninanoncompetitiveantagonisticmanner.ThepD′2valuesofcarbacholandhistaminewere4-45and4-40respectively.EMDinadosedependentmannerprolongedthetimebeforeconsciousguineapigcollapsedinresponsetohistamineaerosolandreducedthenumberofanimalscollapsedduring6min(n=8,P<0-05).CONCLUSIONSEMDinhibitsairwaysmoothmusclecontractionthroughitspotassiumchannelopeningeffectandhasgreatereffectsthanTetasabronchodilatorintheguineapig.TheressynergismbetweenEMDandTet.
出处
《中国药理学通报》
CAS
CSCD
北大核心
1999年第5期440-443,共4页
Chinese Pharmacological Bulletin