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Amelioration of Ischemia/Reperfusion-Induced Myocardial Infarction by the 2-Alkynyladenosine Derivative 2-Octynyladenosine (YT-146)

Sasamori, Jun MSc*; Aihara, Kazuyuki PhD*; Yoneyama, Fumiya PhD*; Sato, Isamu BSc*; Kogi, Kentaro PhD*; Takeo, Satoshi PhD

Journal of Cardiovascular Pharmacology:
doi: 10.1097/01.fjc.0000211739.40336.c5
Original Articles

The present study was aimed at determining whether the novel adenosine A2-agonist YT-146 may have cardioprotective effects against ischemia-reperfusion injury. Anesthetized open-chest dogs underwent 90-min occlusion of the left anterior descending artery and subsequent 300-min reperfusion. The animals were randomly assigned to receive vehicle, 3, or 10 μg/kg YT-146 or ischemic preconditioning (4 episodes of 5 min occlusion followed by 5 min of reperfusion). Blood pressure, heart rate, and regional myocardial blood flow throughout the experiment were measured, as was the myocardial infarct size after reperfusion. The infarct size of the vehicle-treated dog was 56.2%±2.7% (n=5), whereas that of 3 or 10 μg/kg YT-146-treated dog was smaller (ie, 29.5%±8.7% or 20.2%±7.0%, respectively; n=5). The infarct size of the dog treated with 10 μg/kg YT-146 was reduced to a degree similar to that of the ischemic preconditioning (19.2%±6.3%, n=5). YT-146 at both doses elicited a dose-dependent increase in acute hyperemic coronary flow immediately after reperfusion. The cardioprotective effect may be attributed to the limitation of the infarct size, probably via A2-receptor-mediated coronary artery dilatation during the early period of reperfusion.

Author Information

*Drug Research Department, Fukushima Research Laboratories, Toa Eiyo Ltd., Iizaka

Department of Molecular and Cellular Pharmacology, Tokyo University of Pharmacy and Life Science, Hachioji, Japan

Reprints: Jun Sasamori, MSc, Drug Research Department, Fukushima Research Laboratories, Toa Eiyo Ltd., Iizaka, Fukushima, 960-0280 Japan (e-mail:

Received for publication October 7, 2005; accepted March 11, 2006

© 2006 Lippincott Williams & Wilkins, Inc.