Matsumoto N, Matsumura K, Takahashi S, Kimata S, Hirosawa K
Heart Vessels Suppl. 1985;1:187-94. doi: 10.1007/BF02072390.
A new hydroxybenzyl alcohol derivative TA-064 exerts a positive inotropic action in experimental preparations. To assess the acute effects in man, we made a cardiac catheterization study of the hemodynamic responses to TA-064 (20 mg and/or 40 mg given orally) in eleven patients with refractory heart failure due to cardiomyopathy (nine patients with dilated cardiomyopathy and one with amyloidosis). All patients were already receiving full digitalis and diuretics therapy. The following statistically significant (P less than 0.05-0.01) effects were noted: Upon administration of 20 mg of the drug, the cardiac index (CI) increased from a mean +/- 1 SD of 1.6 +/- 0.4 to 2.1 +/- 0.6 l/min/m2; pulmonary capillary wedge pressure (PCW) fell from 25 +/- 5 to 21 +/- 5 mm Hg; right atrial pressure (RA) fell from 12 +/- 3 to 10 +/- 4 mm Hg. In contrast, when 40 mg TA-064 were administered orally, the CI increased from 1.7 +/- 0.4 to 2.4 +/- 0.9 l/min/m2; PCW fell from 25 +/- 8 to 20 +/- 6 mm Hg; pulmonary arterial mean pressure fell from 35 +/- 11 to 29 +/- 9 mm Hg. Neither systemic arterial mean pressure nor heart rate increased. No toxicity was observed. The plasma concentration of TA-064 increased dose-dependently and reached a peak value 0.5-1.5 h after oral administration. Plasma catecholamine levels revealed no significant changes before and after use of the drug; therefore, the mechanism of action may not have been mediated by catecholamine.
一种新的羟基苄醇衍生物TA - 064在实验制剂中表现出正性肌力作用。为评估其对人体的急性效应,我们对11例因心肌病导致难治性心力衰竭的患者(9例扩张型心肌病患者和1例淀粉样变性患者)进行了心脏导管插入术研究,以观察他们对口服TA - 064(20毫克和/或40毫克)的血流动力学反应。所有患者均已接受足量的洋地黄和利尿剂治疗。观察到以下具有统计学意义(P小于0.05 - 0.01)的效应:给予20毫克药物后,心脏指数(CI)从平均±1标准差的1.6±0.4升至2.1±0.6升/分钟/平方米;肺毛细血管楔压(PCW)从25±5降至21±5毫米汞柱;右心房压(RA)从12±3降至10±4毫米汞柱。相比之下,口服40毫克TA - 064时,CI从1.7±0.4升至2.4±0.9升/分钟/平方米;PCW从25±8降至20±6毫米汞柱;肺动脉平均压从35±11降至29±9毫米汞柱。体循环动脉平均压和心率均未升高。未观察到毒性。TA - 064的血浆浓度呈剂量依赖性增加,口服给药后0.5 - 1.5小时达到峰值。血浆儿茶酚胺水平在用药前后无显著变化;因此,其作用机制可能不是由儿茶酚胺介导的。