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新型强心剂DPI 201-106对健康受试者收缩期时间间期及心电图的影响。

The effect of a new inotropic agent, DPI 201-106, on systolic time intervals and the electrocardiogram in healthy subjects.

作者信息

Rüegg P C, Nüesch E

机构信息

Clinical Research Department, Sandoz Ltd, Basel, Switzerland.

出版信息

Br J Clin Pharmacol. 1987 Oct;24(4):453-8. doi: 10.1111/j.1365-2125.1987.tb03197.x.

Abstract
  1. DPI 201-106 (DPI) is a novel inotropic agent, with Na+ channel agonistic action combined with a sensitization of contractile proteins to Ca++. In a double-blind trial in healthy volunteers (n = 20) cardiovascular effects (blood pressure, heart rate, ECG) of single oral doses were studied. In addition systolic time intervals (STIs) were assessed in 10 of these subjects. DPI plasma concentrations were measured by h.p.l.c. 2. Preejection period was shortened by 14 ms (P less than 0.01) and 30 ms (P less than 0.01) 1 h after 30 and 60 mg, respectively, suggesting a dose-dependent inotropic effect. Heart rate was slightly reduced after both doses. Mean blood pressure remained unchanged. 3. Corrected QT interval duration (QTc) was prolonged by a mean of 7 ms (NS) and 22 ms (P less than 0.001) 1 h after 30 and 60 mg, respectively. PQ and QRS intervals remained unaffected. 4. Peak plasma levels were attained at 1-2 h and the terminal elimination half-life was approximately 15 h. 5. It is concluded that DPI has positive inotropic and negative chronotropic properties which make it potentially useful for the treatment of heart failure.
摘要
  1. DPI 201 - 106(DPI)是一种新型的正性肌力药物,具有钠通道激动作用,并能使收缩蛋白对钙离子敏感。在一项针对健康志愿者(n = 20)的双盲试验中,研究了单次口服剂量的心血管效应(血压、心率、心电图)。此外,还对其中10名受试者评估了收缩期时间间期(STIs)。通过高效液相色谱法测定DPI的血浆浓度。2. 分别在服用30毫克和60毫克药物1小时后,射血前期缩短了14毫秒(P < 0.01)和30毫秒(P < 0.01),提示有剂量依赖性正性肌力作用。两种剂量后心率均略有降低。平均血压保持不变。3. 分别在服用30毫克和60毫克药物1小时后,校正QT间期(QTc)平均延长了7毫秒(无统计学意义)和22毫秒(P < 0.001)。PQ和QRS间期未受影响。4. 血浆峰值水平在1 - 2小时达到,终末消除半衰期约为15小时。5. 结论是,DPI具有正性肌力和负性变时性特性,这使其在治疗心力衰竭方面具有潜在用途。

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