Literature DB >> 11864928

Different effects of carvedilol, metoprolol, and propranolol on left ventricular remodeling after coronary stenosis or after permanent coronary occlusion in rats.

Hiroyuki Yaoita1, Atsushi Sakabe, Kazuhira Maehara, Yukio Maruyama.   

Abstract

BACKGROUND: Although carvedilol attenuates left ventricular (LV) remodeling in coronary occlusion-reperfusion, it is not known whether it attenuates ischemic LV remodeling because of coronary stenosis (CS) or permanent coronary occlusion (CO). METHODS AND
RESULTS: We administered a vehicle, carvedilol, propranolol (2, 10, and 30 mg/kg per day, each), metoprolol (6, 30, and 90 mg/kg per day), or bunazosin (0.2 and 1 mg/kg per day), orally for 12 weeks to a total of 608 rats with CS or CO. In these groups and the sham (n=40), we assessed LV function by echocardiography, CS severity, myocardial blood flow and coronary flow reserve, serum ascorbyl free radical, and vitamin C. Both CS and CO increased LV end-diastolic and end-systolic diameters and decreased ejection fraction. The 4 agents failed to attenuate LV remodeling caused by CO. In contrast, the 3 beta-blockers attenuated (P<0.01) or tended to attenuate the increase in LV end-diastolic diameters caused by CS. With similar blood pressure and heart rate lowering by 3 beta-blockers, carvedilol additionally attenuated the increase in end-systolic diameters and improved ejection fraction. The CS reduced myocardial blood flow and coronary flow reserve, which was reversed by carvedilol without modifying the CS severity. Among the 4 agents, only carvedilol decreased ascorbyl free radical and increased vitamin C.
CONCLUSIONS: The effects of beta blockade on ischemic cardiac dysfunction seem to depend on the different properties of the beta-blockers and the doses used. Among the beta-blockers tested, carvedilol provided potent cardioprotection for compromised ischemic but viable myocardium rather than for infarcted myocardium.

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Year:  2002        PMID: 11864928     DOI: 10.1161/hc0802.104503

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  12 in total

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2.  Participation of mast cells in angiogenesis in the border zone of myocardial infarction in rats.

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3.  Antifibrotic Effects of Carvedilol and Impact of Liver Fibrosis on Carvedilol Pharmacokinetics in a Rat model.

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Authors:  Anil Kumar; Samrita Dogra; Atish Prakash
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2009-08-15       Impact factor: 3.000

9.  Rac-induced left ventricular dilation in thyroxin-treated ZmRacD transgenic mice: role of cardiomyocyte apoptosis and myocardial fibrosis.

Authors:  Mohammad T Elnakish; Mohamed D H Hassona; Mazin A Alhaj; Leni Moldovan; Paul M L Janssen; Mahmood Khan; Hamdy H Hassanain
Journal:  PLoS One       Date:  2012-08-24       Impact factor: 3.240

10.  β-AR blockers suppresses ER stress in cardiac hypertrophy and heart failure.

Authors:  Li Ni; Changqing Zhou; Quanlu Duan; Jiagao Lv; Xiangning Fu; Yong Xia; Dao Wen Wang
Journal:  PLoS One       Date:  2011-11-02       Impact factor: 3.240

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