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机构地区:[1]河南医科大学药理教研室 [2]新乡医学院药理教研室
出 处:《中药药理与临床》1997年第4期19-21,共3页Pharmacology and Clinics of Chinese Materia Medica
摘 要:用细胞内微电极技术观察了马钱子碱(brucine)对离体豚鼠乳头肌高K+除极异丙肾上腺素(Iso)和组织胺(His)诱发的慢反应动作电位(SAP)的影响。结果表明,低浓度的brucine延长慢反应动作电位50%、90%动作电位时程(APD50、APD90),较高浓度的brucine则抑制SAP的幅度(APA)、O期最大上升速率(Vmax)以及收缩力(Fc)。将台氏液中Ca2+浓度由2.0mmol/L提高至4.0mmol/L时,brucine对组织胺诱发SAP的APA、Vmax以及Fc的抑制作用反转,提示brucine可能阻滞心肌Ca2+通道。The effects of Brucine were studied on the slow action potentials induced by isoprenaline and histamine in high K + depolarized guinea pig papillary muscles by means of conventional glass microelectrodes. It was demonstrated that Brucine prolonged the slow action potential duration at 50% and 90% repolarization (APD 50 ,APD 90 ).At high concetration, Brucine suppressed the maximal upstroke velocity (Vmax),action potential amplitude (APA) and contractile force(Fc). The inhibitory effects of Brucine on the APA, Vmax and Fc were antagonised partially by the elevation of the extracellular concentration of calcium from 2.0 to 4.0mmol/L. These results indicated that Brucine could block the Ca 2+ channels.
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