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Direct Chronotropic and Inotropic Effects of Mildronate Using Cross-Circulated Dog Atrial and Ventricular Preparations

机译:使用交叉循环狗心房和心室制剂对Mildronate的直接变时性和变力作用

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The cardiac effects of mildronate were studied in isolated and blood-perfused atrial and ventricular preparations from mongrel dogs. Mildronate (10-9-10-6mol) did not induce any chronotropic or inotropic responses in spontaneously beating isolated right atria at 37°C. However, it produced negative chronotropic and inotropic effects at large doses (10-5-10-4mol). Mildronate-induced responses were not significantly inhibited by treatment with atropine, suggesting that they do not involve muscarinic mechanisms. Mildronate produced only a slight negative inotropic effect in electrically paced, isolated left ventricular preparations at extremely large doses. Intravenous injections of 10-4mol/kg mildronate to the support (donor) dog induced a slight, non-significant, depressor effect, and did not significantly influence either atrial pacemaker activity or atrial developed tension. From these results, it is concluded that a therapeutic dose of mildronate has no direct influence on SA nodal pacemaker activity and atrial contractility, but that it has a slight cardiac depressant property at large doses.
机译:在来自杂种犬的分离的和血液灌流的心房和心室制剂中研究了吡ron酸盐的心脏作用。 Mildronate(10-9-10-6mol)在37°C自发跳动的孤立右心房中没有引起任何变时性或变力反应。但是,它在大剂量(10-5-10-4mol)下产生负的变时性和变力作用。阿托品治疗并不能明显抑制Mildronate引起的反应,这表明它们不涉及毒蕈碱机制。 Mildronate在电起搏,隔离的左心室制剂中仅以极大的剂量仅产生轻微的负性肌力作用。给支持犬(供体)静脉注射10-4mol / kg的次膦酸盐诱导轻微的,不显着的降压作用,对心房起搏器活动或心房张力均无明显影响。从这些结果可以得出结论,治疗剂量的次膦酸盐对SA结节律起搏器活性和心房收缩性没有直接影响,但在大剂量时具有轻微的心脏抑制作用。

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