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Cause and effect relationship between myocardial mast cell number and matrix metalloproteinase activity
Department of Anatomy, Physiology and Pharmacology, Auburn University, Auburn, Alabama 36849-5517 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 fistul...
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Published in: | American journal of physiology. Heart and circulatory physiology 2002-08, Vol.283 (2), p.H518-H525 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Department of Anatomy, Physiology and Pharmacology,
Auburn University, Auburn, Alabama 36849-5517
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.
myocardial collagen; gelatinase; cromolyn sodium; aortocaval
fistula; extracellular matrix remodeling |
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ISSN: | 0363-6135 1522-1539 |
DOI: | 10.1152/ajpheart.00218.2000 |