Kino M, Hirota Y, Yamamoto S, Sawada K, Moriguchi M, Kotaka M, Kubo S, Kawamura K
Am J Cardiol. 1983 Mar 1;51(5):802-10. doi: 10.1016/s0002-9149(83)80137-4.
A new inotropic agent, TA-064, (-)-alpha-(3,4-dimethoxyphenethylaminomethyl)-4-hydroxybenzylalcohol, was shown to have strong effects in experimental animals. Its effectiveness and associated adverse effects were tested in humans invasively (n = 6) and noninvasively (n = 17). Increasing doses of intravenous infusion (1, 2, and 4 micrograms/kg/min) increased plasma levels to 15, 35, and 82 ng/ml, respectively, resulting in marked increases in the peak rate of left ventricular pressure rise (dP/dt) (1,450 +/- 63 to 3,042 +/- 349 mm Hg/s) (mean +/- standard error of the mean [SEM], p less than 0.01) and the ratio of dP/dt to left ventricular pressure at a developed pressure of 40 mm Hg (25 +/- 3 to 39 +/- 2 s-1) (p less than 0.01), with a reduction in left ventricular end-diastolic pressure (12 +/- 2 to 4 +/- 1 mm Hg) (p less than 0.01). Minimal or no changes were seen in heart rate and left ventricular systolic pressure. After a single oral dose (10 mg), the plasma level reached its peak at 90 minutes (16 +/- 9 ng/ml, n = 17). A positive inotropic effect was confirmed echocardiographically in both healthy volunteers (n = 8) and patients with congestive heart failure (CHF) (n = 9) who were maximally treated with conventional regimens: increase in mean velocity of circumferential fiber shortening (healthy volunteers: 1.29 +/- 0.05 to 1.60 +/- 0.11 circ/s [p less than 0.05]; patients with CHF: 0.69 +/- 0.08 to 0.93 +/- 0.09 circ/s [p less than 0.01]), ejection fraction (healthy volunteers: 68 +/- 2 to 75 +/- 2% [p less than 0.05], patients with CHF: 37 +/- 4 to 45 +/- 5% [p less than 0.01]) without change in heart rate. The cardiac index was increased only in the CHF group (2.71 +/- 0.22 to 3.21 +/- 0.24 liters/min/m2) (p less than 0.05). No significant untoward effects were observed. Thus TA-064 is a potent inotropic agent and can be used either parenterally or orally. Salutary effects can be expected in patients with congestive heart failure who are treated with digitalis and diuretic agents.
一种新型的强心剂TA-064,即(-)-α-(3,4-二甲氧基苯乙胺甲基)-4-羟基苄醇,在实验动物中显示出强效作用。对其有效性及相关不良反应进行了人体侵入性试验(n = 6)和非侵入性试验(n = 17)。静脉输注剂量递增(1、2和4微克/千克/分钟)时,血浆水平分别升至15、35和82纳克/毫升,导致左心室压力上升峰值速率(dP/dt)显著增加(从1450±63至3042±349毫米汞柱/秒)(平均值±平均标准误差[SEM],p<0.01),在40毫米汞柱的发育压力下dP/dt与左心室压力的比值增加(从25±3至39±2秒-1)(p<0.01),同时左心室舒张末期压力降低(从12±2至4±1毫米汞柱)(p<0.01)。心率和左心室收缩压变化极小或无变化。单次口服剂量(10毫克)后,血浆水平在90分钟时达到峰值(16±9纳克/毫升,n = 17)。在健康志愿者(n = 8)和接受常规方案最大剂量治疗的充血性心力衰竭(CHF)患者(n = 9)中,经超声心动图证实均有正性肌力作用:圆周纤维缩短平均速度增加(健康志愿者:从1.29±0.05至1.60±0.11周/秒[p<0.05];CHF患者:从0.69±0.08至0.93±0.09周/秒[p<0.01]),射血分数增加(健康志愿者:从68±2至75±2%[p<0.05],CHF患者:从37±4至45±5%[p<0.01]),心率无变化。仅CHF组的心指数增加(从2.71±0.22至3.21±0.24升/分钟/平方米)(p<0.05)。未观察到明显的不良影响。因此,TA-064是一种强效强心剂,可通过胃肠外或口服给药。预计在接受洋地黄和利尿剂治疗的充血性心力衰竭患者中会有有益作用。