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机构地区:[1]山东省新药药理研究中心 [2]山东医科大学药学系药理教研室
出 处:《中国药理学通报》1997年第6期541-544,共4页Chinese Pharmacological Bulletin
摘 要:目的:研究关附乙酯(DGFA)对大鼠离体心房肌的作用。方法:常规离体器官实验法。结果:DGFA降低了大鼠离体右心房肌的收缩力(P<0.05)并呈浓度依赖性,对右心房的自律性无明显影响;4μmol·L-1DGFA能显著抑制肾上腺素诱发的大鼠离体左房肌的自律性,药前肾上腺素(AD)的浓度为7.92±2.75μmol·L-1,药后10min,AD的浓度升至16.77±6.12μmol·L-1(n=6,P<0.01);4μmol·L-1DGFA在药后10min,使大鼠离体左房的功能性不应期(FRP),由药前的130±12.6ms延长至150±12.6ms(n=6,P<0.05),但对离体大鼠左房肌的兴奋性无明显影响。结论:DGFA的抗心律失常作用可能与其抑制Na+、Ca2+跨膜转运有关。AIM: The effects of Diacetyl guanfu base A(DGFA) were investigated. METHODS: The contractility, automaticity, functional refractory period(FRP) and excitability of DGFA on isolated rat atrial muscle were studied according to the regular methods. RESULTS: DGFA could depress the contractility of isolated rat right atria in a concentrationmanner, but had little effect on its spontaneous rate compared with vehicle; DGFA (4 μmol·L-1) could remarkably depress the automaticity of isolated rat left atria induced by adrenaline(AD), the concentration of AD rose from 792±275 μmol·L-1 to 1677±612 μmol·L-1 (n=6,P<001); the functional refractory period (FRP) of preparation was prolonged from 130±126 ms to 150±126 ms, (n=6,P<005); but had little effect on the excitability of preparation. CONCLUSION: The antiarrhythmic mechanism of DGFA may be related to its inhibition on Na+ and Ca2+ transmembrane influx.
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