Miao H, Xiao W B, Qin B Y
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing, China.
Zhongguo Yao Li Xue Bao. 1990 Jul;11(4):300-3.
In isolated guinea pig right atria, 7-methoxy-4'-hydroxyl-3'-diethylaminomethylisoflavone (MHDF), a new synthetic isoflavone produced noncompetitive antagonisms to isoproterenol- and histamine-induced positive chronotropic actions with pD'2 values of 5.04 +/- 0.10 and 4.90 +/- 0.18, respectively. MHDF inhibited the positive chronotropic response to CaCl2. In isolated left atria, the negative inotropic action of MHDF increased as the frequency increased. In papillary muscles, MHDF 3 mumol/L reduced the contractile force, while Vmax was decreased and APD and ERP were prolonged. These results indicated that the mechanism of MHDF on myocardium is related to inhibition of Ca2+ influx, Na+ influx and K+ efflux, not by blocking beta or H2 receptors.
在离体豚鼠右心房中,一种新合成的异黄酮7-甲氧基-4'-羟基-3'-二乙氨基甲基异黄酮(MHDF)对异丙肾上腺素和组胺诱导的正性变时作用产生非竞争性拮抗作用,其pD'2值分别为5.04±0.10和4.90±0.18。MHDF抑制对氯化钙的正性变时反应。在离体左心房中,MHDF的负性变力作用随频率增加而增强。在乳头肌中,3μmol/L的MHDF降低收缩力,同时Vmax降低,APD和ERP延长。这些结果表明,MHDF对心肌的作用机制与抑制Ca2+内流、Na+内流和K+外流有关,而非通过阻断β或H2受体。