Sacubitril/Valsartan Averts Adverse Post-Infarction Ventricular Remodeling and Preserves Systolic Function in Rabbits
| Autor: | Adolfo G Mauro, Siddhartha S. Ghosh, Vinh Q Chau, Fadi N Salloum, Francisco Romeo, Teja Devarakonda, Juan Torrado, John A. Nestler, Chad Cain, Anindita Das, Ramzi A Ockaili |
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| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Male medicine.medical_specialty Systole Myocardial Infarction Tetrazoles 030204 cardiovascular system & hematology Sacubitril 03 medical and health sciences Angiotensin Receptor Antagonists Random Allocation 0302 clinical medicine Reperfusion therapy Internal medicine medicine Animals Myocardial infarction Ventricular remodeling Ejection fraction Ventricular Remodeling business.industry Aminobutyrates Biphenyl Compounds Stroke Volume medicine.disease Drug Combinations 030104 developmental biology Valsartan Heart failure Cardiology Rabbits Cardiology and Cardiovascular Medicine business Sacubitril Valsartan medicine.drug |
| Zdroj: | Journal of the American College of Cardiology. 72(19) |
| ISSN: | 1558-3597 |
| Popis: | Background Sacubitril/valsartan (SAC/VAL) is approved by the U.S. Food and Drug Administration for heart failure with reduced ejection fraction (HFrEF). Objectives This study investigated the effects of SAC/VAL on acute myocardial infarction (MI) and cardiac remodeling in a translational rabbit model of MI. Methods New Zealand White rabbits were sedated and underwent conscious MI (45-min ischemia) by balloon inflation (previously implanted surgically) followed by 72 h (acute protocol) or 10 weeks (chronic protocols) of reperfusion. “Infarct-sparing” protocol: SAC/VAL, VAL, or placebo were randomly allocated and administered at reperfusion. “HFrEF-treatment” protocol: rabbits were randomized, and treatment commenced after echocardiography-confirmed left ventricular ejection fraction (LVEF) ≤40%. “HFrEF-prevention” protocol: treatment started at reperfusion and continued daily throughout the study. Results Compared with placebo, SAC/VAL and VAL significantly reduced infarct size (TTC staining) and plasma troponin levels; however, only SAC/VAL preserved LVEF at 72 h post-MI. In the HFrEF-treatment protocol, LVEF improvement was observed with SAC/VAL compared with both placebo and VAL starting 2 weeks post-treatment, a benefit that persisted throughout study duration. In the HFrEF-prevention protocol, SAC/VAL and VAL attenuated the decline in LVEF post-MI, although SAC/VAL offered better functional protection. The functional improvement observed in both treatment protocols was paralleled by significant reduction in left ventricular (LV) scar size (Picrosirius red staining) in the SAC/VAL groups. Conclusions Reperfusion therapy with SAC/VAL or VAL offers robust acute infarct-sparing benefits; however, SAC/VAL treatment offered superior short-term and long-term benefits in preventing MI-induced LV dysfunction compared with VAL. SAC/VAL also significantly attenuated LV scar size following MI compared with placebo, whereas VAL did not reach statistical significance in scar reduction. |
| Databáze: | OpenAIRE |
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