Literature DB >> 12124196

Cause and effect relationship between myocardial mast cell number and matrix metalloproteinase activity.

Gregory L Brower1, Amanda L Chancey, Srihari Thanigaraj, Beatriz B Matsubara, Joseph S Janicki.   

Abstract

The objectives of this study were to investigate the temporal response of left ventricular (LV) matrix metalloproteinase (MMP) activity and collagen volume fraction (CVF) induced by an aortocaval fistula and the role of cardiac mast cells in regulating MMP activity. LV tissue was analyzed for MMP activity, CVF, and mast cell number in rats euthanized at 0.5, 1, 2, 3, 5, 14, 21, 35, and 56 days. Additional rats treated with the mast cell membrane-stabilizing drug cromolyn sodium were euthanized 1, 2, and 3 days postfistula. Marked increases in MMP activity occurred rapidly and remained significantly elevated for 5 days before returning toward normal. A significant decrease in CVF occurred by day 5, but thereafter CVF rebounded to normal or above normal values. The number of myocardial mast cells also significantly increased postfistula, and there was a close association between mast cell density and MMP activity. Cromolyn treatment prevented the increase in mast cell number and MMP activity. Thus it is concluded that cardiac mast cells play a major role in the regulation of MMP activity.

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Year:  2002        PMID: 12124196     DOI: 10.1152/ajpheart.00218.2000

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


  51 in total

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Review 2.  The dynamic interaction between matrix metalloproteinase activity and adverse myocardial remodeling.

Authors:  Joseph S Janicki; Gregory L Brower; Jason D Gardner; Amanda L Chancey; James A Stewart
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3.  Time-dependent remodeling of transmural architecture underlying abnormal ventricular geometry in chronic volume overload heart failure.

Authors:  Hiroshi Ashikaga; Jeffrey H Omens; James W Covell
Journal:  Am J Physiol Heart Circ Physiol       Date:  2004-07-08       Impact factor: 4.733

Review 4.  Cardiac mast cells: the centrepiece in adverse myocardial remodelling.

Authors:  Scott P Levick; Giselle C Meléndez; Eric Plante; Jennifer L McLarty; Gregory L Brower; Joseph S Janicki
Journal:  Cardiovasc Res       Date:  2010-08-24       Impact factor: 10.787

5.  Estrogenic modulation of inflammation-related genes in male rats following volume overload.

Authors:  Jennifer L McLarty; Giselle C Meléndez; Scott P Levick; Shanté Bennett; Tara Sabo-Attwood; Gregory L Brower; Joseph S Janicki
Journal:  Physiol Genomics       Date:  2012-01-24       Impact factor: 3.107

6.  Mast cells and epsilonPKC: a role in cardiac remodeling in hypertension-induced heart failure.

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Review 7.  Substance P in heart failure: the good and the bad.

Authors:  Heather M Dehlin; Scott P Levick
Journal:  Int J Cardiol       Date:  2013-11-12       Impact factor: 4.164

8.  Silymarin attenuated mast cell recruitment thereby decreased the expressions of matrix metalloproteinases-2 and 9 in rat liver carcinogenesis.

Authors:  Gopalakrishnan Ramakrishnan; Sundaram Jagan; Sattu Kamaraj; Pandi Anandakumar; Thiruvengadam Devaki
Journal:  Invest New Drugs       Date:  2008-07-30       Impact factor: 3.850

Review 9.  Cardiac fibroblast: the renaissance cell.

Authors:  Colby A Souders; Stephanie L K Bowers; Troy A Baudino
Journal:  Circ Res       Date:  2009-12-04       Impact factor: 17.367

10.  Early predictors of cardiac decompensation in experimental volume overload.

Authors:  Christelle Oliver-Dussault; Alexis Ascah; Mariannick Marcil; Jimmy Matas; Sylvie Picard; Philippe Pibarot; Yan Burelle; Christian F Deschepper
Journal:  Mol Cell Biochem       Date:  2010-01-07       Impact factor: 3.396

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