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新型正性肌力药物(E,Z)-3-((2-氨基乙氧基)亚氨基)雄甾烷-6,17-二酮盐酸盐(PST2744)的药理学特性

Pharmacological profile of the novel inotropic agent (E,Z)-3-((2-aminoethoxy)imino)androstane-6,17-dione hydrochloride (PST2744).

作者信息

Micheletti R, Mattera G G, Rocchetti M, Schiavone A, Loi M F, Zaza A, Gagnol R J P, De Munari S, Melloni P, Carminati P, Bianchi G, Ferrari P

机构信息

Prassis Sigma-Tau Research Institute, Via Forlanini 1/3, 20019 Settimo Milanese, Italy.

出版信息

J Pharmacol Exp Ther. 2002 Nov;303(2):592-600. doi: 10.1124/jpet.102.038331.

Abstract

The novel Na(+)/K(+)-ATPase inhibitor (E,Z)-3-((2-aminoethoxy)imino)androstane-6,17-dione hydrochloride (PST2744) was characterized for its inotropic and toxic properties. Inhibition potency on dog kidney Na(+)/K(+)-ATPase was comparable (0.43 microM) to that of digoxin (0.45 microM). PST2744 concentration-dependently increased force of contraction in guinea pig atria and twitch amplitude in isolated guinea pig myocytes; in the latter, aftercontractions developed significantly less than with digoxin. Intravenous infusion of 0.2 mg/kg/min PST2744 in anesthetized guinea pigs exerted an immediate and long-lasting inotropic effect (ED(80) of 1.89 +/- 0.37 mg/kg) without causing lethal arrhythmias up to a cumulative dose of 18 mg/kg. Conversely, an equieffective infusion of digoxin (0.016 mg/kg/min; ED(80) of 0.32 mg/kg) caused lethal arrhythmias at a cumulative dose of 0.81 mg/kg. At a higher rate (0.4 mg/kg/min), PST2744 induced lethal arrhythmias, with a lethal dose/ED(80) ratio significantly greater than digoxin (20.2 +/- 6.3 versus 3.23 +/- 0.55, p < 0.05). Decay of the inotropic effect (t(1/2), min) was significantly faster for PST2744 (6.0 +/- 0.39) than for digoxin (18.3 +/- 4.5, p < 0.05). In anesthetized dogs, PST2744 dose-dependently increased maximum velocity of pressure rise (+dP/dt(max)) in the range 32 to 500 microg/kg i.v. and was safer than digoxin. In conscious dogs with a healed myocardial infarction, PST2744 significantly increased resting values of +dP/dt(max), left ventricular pressure, and SPB, and increased +dP/dt(max) throughout treadmill exercise while reverting the increase in left ventricular end diastolic pressure seen in control animals. Digoxin significantly decreased basal heart rate, while not affecting the hemodynamic response to exercise. Thus, PST2744 represents a new class of Na(+)/K(+)-ATPase inhibitors endowed with inotropic activity comparable with that of digitalis but having greater safety.

摘要

新型钠钾ATP酶抑制剂(E,Z)-3-((2-氨基乙氧基)亚氨基)雄甾烷-6,17-二酮盐酸盐(PST2744)的变力性和毒性特性得到了表征。其对犬肾钠钾ATP酶的抑制效力(0.43微摩尔)与地高辛(0.45微摩尔)相当。PST2744浓度依赖性地增加豚鼠心房的收缩力和分离的豚鼠心肌细胞的抽搐幅度;在后者中,后收缩的产生明显少于地高辛。在麻醉的豚鼠中静脉输注0.2毫克/千克/分钟的PST2744产生了即时且持久的变力性作用(ED80为1.89±0.37毫克/千克),在累积剂量达18毫克/千克时未引起致命性心律失常。相反,等效效应输注地高辛(0.016毫克/千克/分钟;ED80为0.32毫克/千克)在累积剂量为0.81毫克/千克时导致致命性心律失常。以更高的速率(0.4毫克/千克/分钟),PST2744诱导致命性心律失常,其致死剂量/ED80比值显著大于地高辛(20.2±6.3对3.23±0.55,p<0.05)。PST2744的变力性作用衰减(t1/2,分钟)明显快于地高辛(6.0±0.39对18.3±4.5,p<0.05)。在麻醉犬中,PST2744在静脉注射剂量为32至500微克/千克范围内剂量依赖性地增加压力上升的最大速度(+dP/dtmax),且比地高辛更安全。在心肌梗死已愈合的清醒犬中,PST2744显著增加+dP/dtmax、左心室压力和收缩压的静息值,并在整个跑步机运动过程中增加+dP/dtmax,同时逆转了对照动物中观察到的左心室舒张末期压力的增加。地高辛显著降低基础心率,而不影响对运动的血流动力学反应。因此,PST2744代表了一类新型的钠钾ATP酶抑制剂,其具有与洋地黄相当的变力性活性,但安全性更高。

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