Research and Development, Pharmacology Department, Sigma-Tau Industrie Farmaceutiche Riunite S.p.A., Via Pontina km 30.400, 00040, Pomezia, Rome, Italy.
Cardiovasc Drugs Ther. 2011 Apr;25(2):133-8. doi: 10.1007/s10557-011-6283-y.
Istaroxime is a new luso-inotropic compound. It exerts inotropic action by reducing Na+/K+-ATPase activity, and simultaneously it stimulates sarcoplasmic reticulum Ca(2+)-ATPase function, thus also inducing lusitropic action. The aim of present study is to assess the effect of chronic istaroxime treatment on cardiac function and heart rate variability in Bio TO.2 Syrian hamster model of progressive heart failure.
Bio TO.2 hamsters were daily treated, from 12 to 28 weeks of age, with 30 mg/kg/day oral istaroxime. Age-matched Bio TO.2 and Bio F1B hamsters were treated with vehicle and used as diseased and healthy controls. At the end of treatment, hearts function and autonomic cardiac control were evaluated.
Hearts from vehicle-treated Bio TO.2 when compared with hearts from Bio F1B showed higher heart/body weight ratio, and lower left ventricular systolic pressure (LVSP), positive and negative derivative of LV pressure (dP/dT), coronary flow rate (CFR). Hearts from istaroxime-treated when compared with those of vehicle-treated hamsters, showed the reduction of heart/body weight ratio, and the increase of LVSP, of both positive and negative dP/dT, and of CFR. Autonomic cardiac control, evaluated by HRV analysis, indicated in vehicle-treated Bio TO.2 hamsters, when compared to healthy, a shift towards increased sympathetic and decreased parasympathetic activities. Istaroxime-treatment preserved parasympathetic activity.
Chronic istaroxime improves cardiac function and heart rate variability in Bio TO.2 Syrian hamster model of progressive heart failure.
伊司他肟是一种新型的正性肌力化合物。它通过降低 Na+/K+-ATP 酶活性发挥正性肌力作用,同时刺激肌浆网 Ca(2+)-ATP 酶的功能,从而也产生正性变力作用。本研究的目的是评估慢性伊司他肟治疗对 Bio TO.2 叙利亚仓鼠进行性心力衰竭模型心脏功能和心率变异性的影响。
从 12 至 28 周龄起,Bio TO.2 仓鼠每天经口给予 30mg/kg/天的伊司他肟治疗。用载体处理年龄匹配的 Bio TO.2 和 Bio F1B 仓鼠,并将其作为患病和健康对照。在治疗结束时,评估心脏功能和自主心脏控制。
与 Bio F1B 心脏相比,载体处理的 Bio TO.2 心脏的心脏/体重比更高,左心室收缩压(LVSP)、LV 压力的正导数和负导数(dP/dT)、冠状动脉血流率(CFR)更低。与载体处理的仓鼠相比,伊司他肟处理的仓鼠的心脏/体重比降低,LVSP、正 dP/dT 和负 dP/dT 以及 CFR 均增加。通过 HRV 分析评估自主心脏控制,与健康仓鼠相比,载体处理的 Bio TO.2 仓鼠的交感神经活动增加,副交感神经活动减少。伊司他肟治疗保留了副交感神经活动。
慢性伊司他肟可改善 Bio TO.2 叙利亚仓鼠进行性心力衰竭模型的心脏功能和心率变异性。