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机构地区:[1]徐州医学院药理教研室
出 处:《药学学报》1994年第7期497-501,共5页Acta Pharmaceutica Sinica
摘 要:6β-乙酰氧基去甲托烷(6β-acetoxynortropane,6β-AN)是一种新型M2受体激动剂,兔10ug·kg-1iv,犬2,5,20ug·kg-1iv均导致呼吸频率、潮气量、每分通气量明显减少(P<0.05或0.01),呈剂量依赖关系。pO2降低,pCO2升高。较小剂量给兔0.5,1.0,2.0,4.0ug·kg-1iva和犬0.25,0.5,1.0ug·kg-1iva亦产生与静脉给药相似的呼吸抑制效应。AF-DX116能拮抗6β-AN的呼吸抑制作用,PZ则与6β-AN产生协同作用。表明6β-AN有呼吸抑制作用,并可能与其激动呼吸中枢M2受体有关。β-AN(6β-acetoxy nortropane),a novel selective M2-receptor agonist,causeddecrease in FR,TV,MVV and pO2 and increase of pCO2 when intravenous injection of 10 ug·kg-1in conscious rabbits or 2,5, 20 ug·kg-1 in conscious dogs was given(P<. 05 or 0.01).Theinhibitory effect on MVV exhibited a dose-dependent relationship.Small doses of 6β-AN icv(0.5,1,2,4 ug·kg-1 in the conscious rabbits)and iva(6.25,0.5 and 1.0 ug·kg-1 in anesthetized dogs)decreased FR,TV,MVV and pO2 and increased pCO2 as well.These results were reversed after admi-nistration of AF-DX116 and enhanced after administration of pirenzepine.Thus,it appears that theinhibitory action of 6β-AN on respiration might be related to stimulation of the inhibitory M2cholinergic receptor in respiratory center.
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