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作 者:李惠兰[1] 王方材[1] 侯云成[1] 梁红媛[1]
机构地区:[1]昆明医学院药理教研室,云南中医学院
出 处:《昆明医学院学报》1994年第2期36-39,共4页Journal of Kunming Medical College
摘 要:用离体实验法研究ι─荷包牡丹碱对豚鼠结肠带收缩的影响,结果发现:ι─荷包牡丹碱明显拮抗组织胺及ca2+引起的收缩,呈现非竞争性拮抗方式,pD'2分别为4.92及5.43.在无ca2+液中,ι─荷包牡丹碱与罂粟碱相似,能抑制组织胺诱发的结肠带收缩.提示两药对结肠带依赖细胞内Ca2+所致的收缩均有明显的抑制,当恢复细胞外Ca2+浓度后,两药对依赖细胞外Ca2+经ROC内流所致的收缩无影响.The contractions induced by histamine or Ca2+ after high K+ depolarization in isolatedguinea─pig taenia coli were markedly inhibited by ι─dicentrine or papaverine. It causedrightward displacement of the dose─response curve for histamine or CaCl2 ι─dicentrinesignificantly depressed maximal response,showing a non─competitive antagonism. The PD2value of ι─dicentrine was 4.92 and 5.3 respectively. in Ca2+ free solution,ι─Dicentrine issimilar to papavering inhibited histamine─induced contraction of guinea─pig taenia coli,which is dependent on Ca2+ released from intracellular store. After Ca2+ concentration inbath solution was restored,ι─dicentrine did not influence the contraction of taenia coli de-pending on extracellular Ca2+.
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