Effect of levosimendan therapy on myocardial infarct size and left ventricular function after acute coronary occlusion

Heart. 2016 Mar;102(6):465-71. doi: 10.1136/heartjnl-2015-308137. Epub 2016 Jan 13.

Abstract

Background: Levosimendan is an inotropic agent with cardioprotective and vasodilating properties used for the management of acutely decompensated heart failure. We studied the effects of levosimendan treatment on the size of myocardial infarction (MI) and left ventricular (LV) function in experimental pig model of post MI heart failure.

Methods: After occlusion of the left anterior descending (LAD) coronary artery, animals received levosimendan 5 mg/kg/day orally for 8 weeks (n=7) or no treatment (n=18). One week after stopping treatment, transthoracic echocardiography, CT scan and positron emission tomography were performed to evaluate myocardial function, perfusion and oxidative metabolism. Histology was used to confirm the size of MI and features of LV remodelling.

Results: The size of MI was significantly smaller in the levosimendan group than in the controls (12±13% vs 27±15% of the LV, p=0.03). End-diastolic volume (EDV) and end-systolic volume (ESV) were smaller in the levosimendan than in the control group (EDV 161±29 mL vs 245±84 mL, p=0.06; ESV 81±18 mL vs 149±67 mL, p=0.03), whereas ejection fraction tended to be higher in the levosimendan group (50±6% vs 41±8%, p=0.06).

Conclusions: Eight weeks of levosimendan therapy after recent LAD occlusion decreases the size of MI and leads to better preservation of LV function as well as reduced LV remodelling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Cardiotonic Agents / therapeutic use
  • Coronary Occlusion / complications*
  • Diastole
  • Disease Models, Animal
  • Follow-Up Studies
  • Hydrazones / therapeutic use*
  • Male
  • Myocardial Contraction / drug effects*
  • Myocardial Contraction / physiology
  • Myocardial Infarction / drug therapy*
  • Myocardial Infarction / etiology
  • Myocardial Infarction / physiopathology
  • Myocardium / pathology*
  • Pyridazines / therapeutic use*
  • Simendan
  • Stroke Volume / drug effects
  • Stroke Volume / physiology
  • Swine
  • Systole
  • Ventricular Function, Left / drug effects*
  • Ventricular Function, Left / physiology
  • Ventricular Remodeling / drug effects*

Substances

  • Cardiotonic Agents
  • Hydrazones
  • Pyridazines
  • Simendan