Background: The natural polyamine Agmatine (Ag) plays a significant role in protection of nerve cell ischemic injury. A previous report indicated that Ag given intraperitoneally to rats enhanced the recovery of the heart from ischemic injury. Based on this initial observation, a larger investigation was undertaken to explore a dose-response effect and possible mechanisms underlying the protective effects. Methods: Using the modified Langendorff model, 36 isolated hearts were divided into five groups: group 1, hearts receiving 100 μM/L Ag pre-ischemia (n=7); group 2, hearts receiving 100 μM/L Ag pre- and post-ischemia, (n=7); group 3, hearts receiving 250 μM/L Ag pre-ischemia (n=7); group 4, hearts receiving 250 μM/L Ag pre- and postischemia (n=7); and group 5, hearts receiving Krebs-Hensleit solution served as control (n=8). The study design included 20 minutes of perfusion, 30 minutes of global ischemia, and 30 minutes of reperfusion. Results: After ischemia, group 2 developed higher left ventricular pressure P(max) (P<0.01), improved first-derivative of the rise (dP/dt max; P<;0.02), and fall (dP/dt min; P<0.04) in left ventricular pressure, and the area calculated under the left-ventricle developed pressure curve (pressure-time integral; P<0.015), but coronary flow was not significantly increased (P=0.06) compared to the control group. Group 1 had improved diastolic recovery: dP/dt min (P<0.05) and coronary flow (P<0.03), compared with the control group. Group 3 had improved P(max) (P<0.01), dP/dt min (P<0.01), and coronary flow (P<0.02); group 4 had no improvement in ali hemodynamic parameters. Conclusion: Low doses of Ag given pre- and post-ischemia, and high doses given only preischemia have favorable, protective effects on the hemodynamic recovery of isolated rat heart undergoing global ischemia and reperfusion.
|Number of pages||9|
|Journal||Journal of Cardiovascular Pharmacology and Therapeutics|
|State||Published - 2001|
- Isolated heart