Literature DB >> 16210139

Long-term therapy with the acorn cardiac support device normalizes gene expression of growth factors and gelatinases in dogs with heart failure.

Sharad Rastogi1, Ramesh C Gupta, Sudhish Mishra, Hideaki Morita, Elaine J Tanhehco, Hani N Sabbah.   

Abstract

BACKGROUND: Passive mechanical containment of the failing left ventricle with the Acorn Cardiac Support Device (CSD) was shown to prevent progressive left ventricular dilation in dogs with heart failure and increase left ventricular ejection fraction. To examine possible mechanisms for improved cardiac function with a CSD, we examined the effect of CSD therapy on the mRNA gene expression of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), matrix metalloproteinases (MMP) 2 and 9, and tissue inhibitors of metalloproteinases (TIMP) 1 and 2.
METHODS: Heart failure was produced in 12 dogs by multiple sequential intracoronary microembolizations. Six dogs were implanted with the CSD and 6 served as concurrent controls. Left ventricular tissue from 6 normal dogs was used for comparison.
RESULTS: Compared with normal dogs, dogs with untreated heart failure showed downregulation of mRNA expression for VEGF and bFGF, whereas upregulation of mRNA expression for MMP-2 and MMP-9 was observed. Normalization of mRNA expression for all these genes was seen after treatment with the CSD.
CONCLUSIONS: This study shows that preventing left ventricular dilation and myocardial stretch with the CSD promotes normalization of growth factor and MMP gene expression. These results suggest that modulation of gene activity may, in part, contribute to the improvement of left ventricular function observed with CSD therapy.

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Year:  2005        PMID: 16210139     DOI: 10.1016/j.healun.2004.07.022

Source DB:  PubMed          Journal:  J Heart Lung Transplant        ISSN: 1053-2498            Impact factor:   10.247


  7 in total

Review 1.  Surgical aspects of congestive heart failure.

Authors:  Daniel J Goldstein; Douglas Smego; Robert E Michler
Journal:  Heart Fail Rev       Date:  2006-06       Impact factor: 4.214

2.  Myocardial transfection with naked DNA plasmid encoding hepatocyte growth factor prevents the progression of heart failure in dogs.

Authors:  Sharad Rastogi; Mayra Guerrero; Mengjun Wang; Itamar Ilsar; Michael S Sabbah; Ramesh C Gupta; Hani N Sabbah
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-01-07       Impact factor: 4.733

3.  Effects of cyclic mechanical stretch on extracellular matrix synthesis by human scleral fibroblasts.

Authors:  Lilian Shelton; Jody Summers Rada
Journal:  Exp Eye Res       Date:  2006-11-21       Impact factor: 3.467

Review 4.  Modulation of left ventricular dilation remodeling with epicardial restraint devices in postmyocardial infarction heart failure.

Authors:  Veli K Topkara; Srikanth Kondareddy; Douglas L Mann
Journal:  Curr Heart Fail Rep       Date:  2009-12

5.  Adiponectin attenuates profibrotic extracellular matrix remodeling following cardiac injury by up-regulating matrix metalloproteinase 9 expression in mice.

Authors:  Alexander Jenke; Robert Schur; Carsten Röger; Zehra Karadeniz; Mathias Grüger; Luise Holzhauser; Kostas Savvatis; Wolfgang Poller; Heinz-Peter Schultheiss; Ulf Landmesser; Carsten Skurk
Journal:  Physiol Rep       Date:  2017-12

6.  Leptin signaling in the failing and mechanically unloaded human heart.

Authors:  Kenneth R McGaffin; Christine S Moravec; Charles F McTiernan
Journal:  Circ Heart Fail       Date:  2009-08-19       Impact factor: 8.790

7.  Expression and complex formation of MMP9, MMP2, NGAL, and TIMP1 in porcine myocardium but not in skeletal muscles in male pigs with tachycardia-induced systolic heart failure.

Authors:  Liliana Kiczak; Alicja Tomaszek; Jacek Bania; Urszula Paslawska; Maciej Zacharski; Agnieszka Noszczyk-Nowak; Adrian Janiszewski; Piotr Skrzypczak; Hossein Ardehali; Ewa A Jankowska; Piotr Ponikowski
Journal:  Biomed Res Int       Date:  2013-04-22       Impact factor: 3.411

  7 in total

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