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Ann Thorac Surg 1998;65:474-479
© 1998 The Society of Thoracic Surgeons


Original Articles: Cardiovascular

Effects of an Angiotensin II Antagonist on Ischemic and Nonischemic Isolated Rat Hearts

Yosef Paz, MD, Jacob Gurevitch, MD, Inna Frolkis, MD, PhD, Menachem Matsa, MD, Amir Kramer, MD, Chaim Locker, MD, Rephael Mohr, MD, Gad Keren, MD

Department of Thoracic and Cardiovascular Surgery, Elias Sourasky-Tel-Aviv Medical Center, Tel-Aviv, Israel
Department of Cardiology, Elias Sourasky-Tel-Aviv Medical Center, Tel-Aviv, Israel

Accepted for publication August 19, 1997.

Dr Gurevitch, Department of Thoracic and Cardiovascular Surgery, Ichilov Hospital, Elias Sourasky-Tel-Aviv Medical Center, 6 Weizman St, Tel-Aviv 64239, Israel.

Background. Increasing evidence suggests that a locally integrated or intramyocardial renin-angiotensin system plays a significant role in ischemia-reperfusion injury. We evaluated the effects of losartan, an angiotensin II type 1 receptor blocking agent, on ischemic and nonischemic isolated rat hearts.

Methods. Using the modified Langendorff model, hearts were perfused with either low or high doses of losartan (18.2 mmol/L or 182.2 mmol/L, respectively) or with saline added to Krebs-Henseleit solution during phase I of the study. During phase II, hearts were exposed to a 60-minute period of global ischemia. Ischemic arrest was induced with warm cardioplegic solution (KCl, 16 mEq/L) containing either high-dose losartan (182.2 mmol/L) or Krebs-Henseleit solution only.

Results. During phase I of the study, no statistically significant differences were observed between the low-dose losartan group and the control group. However, hearts treated with high-dose losartan demonstrated an increase in peak systolic pressure, maximum first derivative of pressure, pressure-time integral, coronary flow, and oxygen consumption (p < 0.0001). During phase II, hearts treated with losartan showed a significantly better recovery on reperfusion, as reflected by better contractility (p < 0.001), higher oxygen consumption (p < 0.001), higher coronary flow (p < 0.0001), and lower creatine phosphokinase levels (41.1 ± 1.7 versus 73.3 ± 5.6 U/L; p < 0.001).

Conclusions. High doses of losartan have a positive inotropic effect on normally perfused hearts. Given in cardioplegic solution, the drug has a significant protective effect on ischemic isolated rat hearts.




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