Timing and duration of administration are crucial for antiinfarct effect of AMP 579 infused at reperfusion in rabbit heart.

Zhelong Xu, James M Downey, Michael V Cohen
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引用次数: 39

Abstract

The adenosine A(1)/A(2) receptor agonist AMP 579 has been reported to protect the heart against infarction even when administered after the onset of ischemia. The present study explored both the timing and the duration of treatment required to limit infarct size in in situ rabbit hearts subjected to 30 min of regional ischemia and 3 hours of reperfusion. In groups 1 and 2, AMP 579 was infused from 10 min before reperfusion and continued for either 30 or 40 min. In group 3, AMP 579 was begun at the onset of reperfusion and continued for 70 min. In group 4, AMP 579 was also infused for 70 min but begun 10 min after reperfusion. In untreated hearts 36.4 +/- 3.1% of the risk zone infarcted. Protection was observed only in hearts having a 70-minute infusion of AMP 579 starting at reperfusion (13.0 +/- 1.9%, P < 0.05). Therefore, AMP 579 must be present at the moment of reperfusion and have a continued presence of more than 30 min thereafter to protect. Importantly, because AMP 579 can protect when administered up to the time of reperfusion, it likely prevents a reperfusion injury, and, therefore, has impressive clinical potential.

AMP 579在兔心脏再灌注时给药的时间和持续时间对其抗梗死作用至关重要。
据报道,腺苷A(1)/A(2)受体激动剂AMP 579即使在缺血发作后给予也能保护心脏免受梗死。本研究探讨了局部缺血30分钟和再灌注3小时的原位兔心脏限制梗死面积所需的治疗时间和持续时间。在1组和2组中,AMP 579从再灌注前10分钟开始注射,持续30或40分钟。在3组中,AMP 579在再灌注开始时开始注射,持续70分钟。在4组中,AMP 579也持续70分钟,但在再灌注后10分钟开始注射。在未治疗的心脏中,36.4 +/- 3.1%的危险区发生梗死。仅在再灌注时开始注射AMP 579 70分钟的心脏中观察到保护作用(13.0 +/- 1.9%,P < 0.05)。因此,AMP 579必须在再灌注时存在,并在再灌注后持续存在30分钟以上才能起到保护作用。重要的是,由于AMP 579在再灌注时可以起到保护作用,因此它可能防止再灌注损伤,因此具有令人印象深刻的临床潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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