Department of Medicine, Division of Cardiovascular Medicine, Henry Ford Hospital, 2799 West Grand Boulevard, Detroit, MI, 48202, USA.
Cardiovasc Drugs Ther. 2013 Dec;27(6):489-98. doi: 10.1007/s10557-013-6482-9.
GP531 is a second generation adenosine regulating agent (ARA) that increases concentrations of endogenous adenosine, a natural cardioprotective agent, in ischemic/hypoxic tissue. This study examined the effects of acute intravenous infusions of GP531 on left ventricular (LV) systolic and diastolic function in dogs with advanced chronic heart failure (HF) (LV ejection fraction, EF <30 %).
Six dogs with intracoronary microembolization-induced HF received a constant intravenous infusion of GP531 (10 μg/kg/min) or vehicle (normal saline) for 6 h in random order 1 week apart. Hemodynamic measurements were made at baseline and at 1, 2, 3, 4, 5 and 6 h after initiating drug infusion. Myocardial oxygen consumption (MVO2) was measured at baseline and 4 and 6 h. LV pressure-volume relationship (PVR) was measured at baseline and 6 h.
Vehicle infusions had no effect on indexes of LV systolic and diastolic function. GP531 infusion had no effect on heart rate or mean aortic pressure but significantly decreased LV end-diastolic pressure, end-diastolic volume, end-systolic volume and end-diastolic wall stress. GP531 significantly increased LV EF (27 ± 1 at baseline to 34 ± 1 after 6 h of drug infusion, p < 0.05), deceleration time of early mitral inflow velocity and the slope of end-systolic PVR without increasing MVO2.
Results of the study indicate that approaches which increase the local release of adenosine in failing LV myocardium, such as ARAs, have a favorable impact on LV performance. These observations support the continued development of ARA's for the treatment of acute HF syndromes.
GP531 是一种第二代腺苷调节剂(ARA),可增加缺血/缺氧组织中内源性腺苷(一种天然的心脏保护剂)的浓度。本研究探讨了急性静脉输注 GP531 对患有晚期慢性心力衰竭(HF)(左心室射血分数,EF <30%)犬左心室(LV)收缩和舒张功能的影响。
6 只犬通过冠状动脉内微栓塞诱导 HF,随机间隔 1 周接受 GP531(10μg/kg/min)或载体(生理盐水)持续静脉输注 6 小时。在开始药物输注后 1、2、3、4、5 和 6 小时进行血流动力学测量。在基线和 4 小时和 6 小时测量心肌耗氧量(MVO2)。在基线和 6 小时测量 LV 压力-容积关系(PVR)。
载体输注对 LV 收缩和舒张功能指标没有影响。GP531 输注对心率或平均主动脉压没有影响,但显著降低 LV 舒张末期压力、舒张末期容积、收缩末期容积和舒张末期壁应力。GP531 显著增加 LV EF(基线时为 27±1,6 小时药物输注后为 34±1,p<0.05)、早期二尖瓣流入速度减速时间和收缩末期 PVR 斜率,而不增加 MVO2。
研究结果表明,增加衰竭 LV 心肌中腺苷局部释放的方法,如 ARA,对 LV 性能有有利影响。这些观察结果支持继续开发 ARA 治疗急性 HF 综合征。