atorvastatin therapy during the peri-infarct period attenuates left ventricular dysfunction and remodeling after myocardial infarction阿托伐他汀治疗peri-infarct期间减弱心肌梗死后左心室功能障碍和重构.pdfVIP

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atorvastatin therapy during the peri-infarct period attenuates left ventricular dysfunction and remodeling after myocardial infarction阿托伐他汀治疗peri-infarct期间减弱心肌梗死后左心室功能障碍和重构.pdf

atorvastatin therapy during the peri-infarct period attenuates left ventricular dysfunction and remodeling after myocardial infarction阿托伐他汀治疗peri-infarct期间减弱心肌梗死后左心室功能障碍和重构

Atorvastatin Therapy during the Peri-Infarct Period Attenuates Left Ventricular Dysfunction and Remodeling after Myocardial Infarction 1. 1. 1 1 1 2 Xian-Liang Tang , Santosh K. Sanganalmath , Hiroshi Sato , Qiuli Bi , Greg Hunt , Robert J. Vincent , 1 1 2 1 Yong Peng , Gregg Shirk , Buddhadeb Dawn , Roberto Bolli * 1 Division of Cardiovascular Medicine and Institute of Molecular Cardiology, University of Louisville, Louisville, Kentucky, United States of America, 2 Cardiovascular Research Institute, Kansas University Medical Center, Kansas City, Kansas, United States of America Abstract Although statins impart a number of cardiovascular benefits, whether statin therapy during the peri-infarct period improves subsequent myocardial structure and function remains unclear. Thus, we evaluated the effects of atorvastatin on cardiac function, remodeling, fibrosis, and apoptosis after myocardial infarction (MI). Two groups of rats were subjected to permanent coronary occlusion. Group II (n = 14) received oral atorvastatin (10 mg/kg/d) daily for 3 wk before and 4 wk after MI, while group I (n = 12) received equivalent doses of vehicle. Infarct size (Masson’s trichrome-stained sections) was similar in both groups. Compared with group I, echocardiographic left ventricular ejection fraction (LVEF) and fractional area change (FAC) were higher while LV end-diastolic volume (LVEDV) and LV end-systolic and end-diastolic diameters (LVESD and LVEDD) were lower in treated rats. Hemodynamically, atorvastatin-treated rats exhibited significantly higher dP/dtmax, end-systol

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