Literature DB >> 24781435

The multiple mechanistic faces of a pure volume overload: implications for therapy.

Justin Barnes1, Louis J DellʼItalia.   

Abstract

: Mitral regurgitation and other conditions marked by a pure isolated volume overload (VO) of the heart result in a progressive form of eccentric left ventricular remodeling and dysfunction. As opposed to the more extensively studied pressure overload, there are no approved medical therapies because an understanding of the underlying pathological mechanisms at work in VO is lacking. Over the past 20 years, our laboratory has identified multiple key biological functions involved in the pathological remodeling in VO. Specifically, we have noted perturbed matrix homeostasis, detrimental adrenergic signaling, increased intracellular reactive oxygen species and an intense inflammatory response that implicates mast cells and their product chymase, which seems to cause extensive remodeling both inside and outside the cardiomyocyte. How these multiple pathways intersect over the course of VO and their response to various single and combined interventions are now the subject of intense investigation.

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Year:  2014        PMID: 24781435      PMCID: PMC4504010          DOI: 10.1097/MAJ.0000000000000255

Source DB:  PubMed          Journal:  Am J Med Sci        ISSN: 0002-9629            Impact factor:   2.378


  53 in total

1.  Dog mast cell alpha-chymase activates progelatinase B by cleaving the Phe88-Gln89 and Phe91-Glu92 bonds of the catalytic domain.

Authors:  K C Fang; W W Raymond; J L Blount; G H Caughey
Journal:  J Biol Chem       Date:  1997-10-10       Impact factor: 5.157

2.  Inactivation of focal adhesion kinase in cardiomyocytes promotes eccentric cardiac hypertrophy and fibrosis in mice.

Authors:  Xu Peng; Marc S Kraus; Huijun Wei; Tang-Long Shen; Romain Pariaut; Ana Alcaraz; Guangju Ji; Lihong Cheng; Qinglin Yang; Michael I Kotlikoff; Ju Chen; Kenneth Chien; Hua Gu; Jun-Lin Guan
Journal:  J Clin Invest       Date:  2005-12-22       Impact factor: 14.808

Review 3.  Chymase and matrix metalloproteinase.

Authors:  Hidenori Urata
Journal:  Hypertens Res       Date:  2007-01       Impact factor: 3.872

4.  Isolation and identification of proangiotensin-12, a possible component of the renin-angiotensin system.

Authors:  Sayaka Nagata; Johji Kato; Kazuki Sasaki; Naoto Minamino; Tanenao Eto; Kazuo Kitamura
Journal:  Biochem Biophys Res Commun       Date:  2006-10-05       Impact factor: 3.575

5.  Mast cells cause apoptosis of cardiomyocytes and proliferation of other intramyocardial cells in vitro.

Authors:  M Hara; A Matsumori; K Ono; H Kido; M W Hwang; T Miyamoto; A Iwasaki; M Okada; K Nakatani; S Sasayama
Journal:  Circulation       Date:  1999-09-28       Impact factor: 29.690

6.  Beta1-adrenoceptor blockade mitigates excessive norepinephrine release into cardiac interstitium in mitral regurgitation in dog.

Authors:  Gerald H Hankes; Jeffrey L Ardell; José Tallaj; Chih-Chang Wei; Inmaculada Aban; Merrilee Holland; Patricia Rynders; Ray Dillon; Rene Cardinal; Donald B Hoover; J Andrew Armour; Ahsan Husain; Louis J Dell'Italia
Journal:  Am J Physiol Heart Circ Physiol       Date:  2006-07       Impact factor: 4.733

7.  Pharmacologic inhibition of mast cell degranulation prevents left ventricular remodeling induced by chronic volume overload in rats.

Authors:  Gregory L Brower; Joseph S Janicki
Journal:  J Card Fail       Date:  2005-09       Impact factor: 5.712

8.  Left ventricular eccentric remodeling and matrix loss are mediated by bradykinin and precede cardiomyocyte elongation in rats with volume overload.

Authors:  Thomas D Ryan; Emily C Rothstein; Inmaculada Aban; Jose A Tallaj; Ahsan Husain; Pamela A Lucchesi; Louis J Dell'Italia
Journal:  J Am Coll Cardiol       Date:  2007-02-05       Impact factor: 24.094

9.  Mechanisms of cardiac hypertrophy in canine volume overload.

Authors:  T Matsuo; B A Carabello; Y Nagatomo; M Koide; M Hamawaki; M R Zile; P J McDermott
Journal:  Am J Physiol       Date:  1998-07

10.  Mast cell chymase induces smooth muscle cell apoptosis by disrupting NF-kappaB-mediated survival signaling.

Authors:  Markus J Leskinen; Hanna M Heikkilä; Mei Y Speer; Jukka K Hakala; Mika Laine; Petri T Kovanen; Ken A Lindstedt
Journal:  Exp Cell Res       Date:  2006-02-07       Impact factor: 3.905

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  4 in total

1.  Cardiac Tissue Chips (CTCs) for Modeling Cardiovascular Disease.

Authors:  Aaron J Rogers; Jessica M Miller; Ramaswamy Kannappan; Palaniappan Sethu
Journal:  IEEE Trans Biomed Eng       Date:  2019-03-18       Impact factor: 4.538

2.  Cardiomyocyte mitochondrial oxidative stress and cytoskeletal breakdown in the heart with a primary volume overload.

Authors:  Danielle M Yancey; Jason L Guichard; Mustafa I Ahmed; Lufang Zhou; Michael P Murphy; Michelle S Johnson; Gloria A Benavides; James Collawn; Victor Darley-Usmar; Louis J Dell'Italia
Journal:  Am J Physiol Heart Circ Physiol       Date:  2015-01-16       Impact factor: 4.733

3.  Cardiac remodeling secondary to chronic volume overload is attenuated by a novel MMP9/2 blocking antibody.

Authors:  Lena Cohen; Irit Sagi; Einat Bigelman; Inna Solomonov; Anna Aloshin; Jeremy Ben-Shoshan; Zach Rozenbaum; Gad Keren; Michal Entin-Meer
Journal:  PLoS One       Date:  2020-04-09       Impact factor: 3.240

4.  Transcriptional Changes Associated with Long-Term Left Ventricle Volume Overload in Rats: Impact on Enzymes Related to Myocardial Energy Metabolism.

Authors:  Elise Roussel; Marie-Claude Drolet; Elisabeth Walsh-Wilkinson; Wahiba Dhahri; Dominic Lachance; Suzanne Gascon; Otman Sarrhini; Jacques A Rousseau; Roger Lecomte; Jacques Couet; Marie Arsenault
Journal:  Biomed Res Int       Date:  2015-10-25       Impact factor: 3.411

  4 in total

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