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Myocardial Interstitial Matrix Metalloproteinase Activity Is Altered by Mechanical Changes in LV Load: Interaction With the Angiotensin Type 1 Receptor

LV myocardial remodeling is a structural hallmark of hypertensive hypertrophy, but molecular mechanisms driving this process are not well understood. The matrix metalloproteinases (MMPs) can cause myocardial remodeling in chronic disease states, but how MMP activity is altered with a mechanical load...

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Published in:Circulation research 2005-05, Vol.96 (10), p.1110-1118
Main Authors: Deschamps, Anne M, Apple, Kimberly A, Leonardi, Amy H, McLean, Julie E, Yarbrough, William M, Stroud, Robert E, Clark, Leslie L, Sample, Jeffrey A, Spinale, Francis G
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container_issue 10
container_start_page 1110
container_title Circulation research
container_volume 96
creator Deschamps, Anne M
Apple, Kimberly A
Leonardi, Amy H
McLean, Julie E
Yarbrough, William M
Stroud, Robert E
Clark, Leslie L
Sample, Jeffrey A
Spinale, Francis G
description LV myocardial remodeling is a structural hallmark of hypertensive hypertrophy, but molecular mechanisms driving this process are not well understood. The matrix metalloproteinases (MMPs) can cause myocardial remodeling in chronic disease states, but how MMP activity is altered with a mechanical load remains unknown. The present study quantified interstitial MMP activity after a discrete increase in LV load and dissected out the contributory role of the angiotensin II Type 1 receptor (AT1R). Pigs (38kg) were randomized to undergo (1) increased LV load by insertion of an intra-aortic balloon pump (IABP) triggered at systole for 3 hours, then deactivated (n=11); (2) IABP and AT1R blockade (AT1RB; valsartan, 3 ng/kg/hr; n=6). MMP activity was directly measured in the myocardial interstitium using a validated inline digital fluorogenic microdialysis system. IABP engagement increased LV peak pressure from 92±3 to 113±5 and 123±7 mm Hg in the vehicle and AR1RB group, respectively, and remained elevated throughout the IABP period (P
doi_str_mv 10.1161/01.RES.0000167830.12010.6b
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subjects Angiotensin II Type 1 Receptor Blockers - pharmacology
Animals
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Hypertension - enzymology
Hypertension - physiopathology
Intra-Aortic Balloon Pumping
Matrix Metalloproteinases - metabolism
Myocardium - enzymology
Receptor, Angiotensin, Type 1 - physiology
Swine
Ventricular Function, Left
Ventricular Remodeling
Vertebrates: cardiovascular system
title Myocardial Interstitial Matrix Metalloproteinase Activity Is Altered by Mechanical Changes in LV Load: Interaction With the Angiotensin Type 1 Receptor
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