Literature DB >> 15665053

Impaired resting perfusion in viable myocardium distal to chronic coronary stenosis in rats.

Christiane Waller1, Tobias Engelhorn, Karl-Heinz Hiller, Gerd Heusch, Georg Ertl, Wolfgang Rudolf Bauer, Rainer Schulz.   

Abstract

Chronic coronary artery stenosis results in patchy necrosis in the dependent myocardium and impairs global and regional left ventricular (LV) function in rats in vivo. The aim of the present study was to compare regional myocardial blood flow (RMBF) and function (F) in poststenotic myocardium by using magnetic resonance imaging (MRI) and to compare MRI blood flow changes to histological alterations to assess whether RMBF in the viable poststenotic tissue remains normal. MRI was performed in 11 anesthetized Wistar rats with 2-wk stenosis of the left coronary artery. Postmortem, the extent of fibrotic tissue was quantified. Poststenotic RMBF was significantly reduced to 2.21 +/- 0.30 ml.g(-1).min(-1) compared with RMBF in the remote myocardium (4.05 +/- 0.50 ml.g(-1).min(-1)). A significant relationship between the poststenotic RMBF (%remote area) and the poststenotic F (%remote myocardium) was calculated (r = 0.61, P < 0.05). Assuming perfusion in scar tissue to be 32 +/- 5% of perfusion of remote myocardium, as measured in five additional rats, and that in remote myocardium to be 114 +/- 25% of that in normal myocardium, as assessed in five sham rats, the calculated perfusion in partially fibrotic tissue samples (35.7 +/- 5.2% of analyzed area) was 2.88 +/- 0.18 ml.g(-1).min(-1), whereas measured MRI perfusion was only 1.86 +/- 0.24 ml.g(-1).min(-1) (P < 0.05). These results indicate that resting perfusion in viable poststenotic myocardium is moderately reduced. Alterations in global and regional LV function are therefore secondary to both patchy fibrosis and reduced resting perfusion.

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Year:  2005        PMID: 15665053     DOI: 10.1152/ajpheart.01060.2004

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  5 in total

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Journal:  Magn Reson Med       Date:  2010-03       Impact factor: 4.668

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Authors:  Moriel H Vandsburger; Frederick H Epstein
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Authors:  Steffen Bohl; Craig A Lygate; Hannah Barnes; Debra Medway; Lee-Anne Stork; Jeanette Schulz-Menger; Stefan Neubauer; Jurgen E Schneider
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-02-13       Impact factor: 4.733

4.  Improve myocardial T1 measurement in rats with a new regression model: application to myocardial infarction and beyond.

Authors:  Haosen Zhang; Qing Ye; Jie Zheng; Erik B Schelbert; T Kevin Hitchens; Chien Ho
Journal:  Magn Reson Med       Date:  2013-10-18       Impact factor: 4.668

5.  First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart.

Authors:  Daniel J Stuckey; Carolyn A Carr; Stephanie J Meader; Damian J Tyler; Mark A Cole; Kieran Clarke
Journal:  J Cardiovasc Magn Reson       Date:  2011-08-03       Impact factor: 5.364

  5 in total

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