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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 |
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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 |
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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<0.05). With IABP disengagement, segmental shortening (% change from baseline of 0) remained depressed in the vehicle group (-32.2±11.8%, P<0.05) but returned to baseline in the AT1RB group (2.3±12.5%). MMP activity decreased with IABP in both groups. At IABP disengagement, a surge in MMP activity occurred in the vehicle group that was abrogated with AT1RB (3.03±0.85 versus 0.07±1.55 MMP units/hr, P<0.05). A transient increase in LV load caused a cyclic variation in interstitial MMP activity that is regulated in part by the AT1R. These temporally dynamic changes in MMP activity likely influence myocardial function and structure with increased LV load.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/01.RES.0000167830.12010.6b</identifier><identifier>PMID: 15860759</identifier><identifier>CODEN: CIRUAL</identifier><language>eng</language><publisher>Hagerstown, MD: American Heart Association, Inc</publisher><subject>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</subject><ispartof>Circulation research, 2005-05, Vol.96 (10), p.1110-1118</ispartof><rights>2005 American Heart Association, Inc.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4023-8a55d5bf377df8bd422c5620bb1b5973c4f11862d8e1a57ce12090ad35519e5e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16915635$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15860759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deschamps, Anne M</creatorcontrib><creatorcontrib>Apple, Kimberly A</creatorcontrib><creatorcontrib>Leonardi, Amy H</creatorcontrib><creatorcontrib>McLean, Julie E</creatorcontrib><creatorcontrib>Yarbrough, William M</creatorcontrib><creatorcontrib>Stroud, Robert E</creatorcontrib><creatorcontrib>Clark, Leslie L</creatorcontrib><creatorcontrib>Sample, Jeffrey A</creatorcontrib><creatorcontrib>Spinale, Francis G</creatorcontrib><title>Myocardial Interstitial Matrix Metalloproteinase Activity Is Altered by Mechanical Changes in LV Load: Interaction With the Angiotensin Type 1 Receptor</title><title>Circulation research</title><addtitle>Circ Res</addtitle><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<0.05). With IABP disengagement, segmental shortening (% change from baseline of 0) remained depressed in the vehicle group (-32.2±11.8%, P<0.05) but returned to baseline in the AT1RB group (2.3±12.5%). MMP activity decreased with IABP in both groups. At IABP disengagement, a surge in MMP activity occurred in the vehicle group that was abrogated with AT1RB (3.03±0.85 versus 0.07±1.55 MMP units/hr, P<0.05). A transient increase in LV load caused a cyclic variation in interstitial MMP activity that is regulated in part by the AT1R. These temporally dynamic changes in MMP activity likely influence myocardial function and structure with increased LV load.</description><subject>Angiotensin II Type 1 Receptor Blockers - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hypertension - enzymology</subject><subject>Hypertension - physiopathology</subject><subject>Intra-Aortic Balloon Pumping</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>Myocardium - enzymology</subject><subject>Receptor, Angiotensin, Type 1 - physiology</subject><subject>Swine</subject><subject>Ventricular Function, Left</subject><subject>Ventricular Remodeling</subject><subject>Vertebrates: cardiovascular system</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpFkV1v0zAUhi0EYt3gLyALCe5S_BHHye6qaoxKrZDGgEvLcU4WQ5p0tsvIL-HvcrpWqm_89bzvsc9LyHvO5pwX_BPj87ubb3OGgxe6lHgsGF4W9Qsy40rkWa40f0lmCFSZlpJdkMsYfyGeS1G9JhdclQXTqpqRf5tpdDY03vZ0NSQIMfl02GxsCv4v3UCyfT_uwpjADzYCXbjk__g00VWkix4V0NB6QtB1dvAOpUtcPECkfqDrH3Q92ub66G1ROg70p08dTR1aDQ8efYeI5P20A8rpHTjYpTG8Ia9a20d4e5qvyPfPN_fLL9n66-1quVhnLmdCZqVVqlF1K7Vu2rJuciGcKgSra16rSkuXt5yXhWhK4FZpB9ipitlGKsUrUCCvyMejL_7wcQ8xma2PDvreDjDuo8H-6pwzieD1EXRhjDFAa3bBb22YDGfmEIth3GAs5hyLeY7FFDWK352q7OstNGfpKQcEPpwAG7GFbbCD8_HMFRVXhVTI5UfuaTy0Pv7u908QTAe2T91zacm4yARjiimhWXZ4jJT_AYs5p0U</recordid><startdate>20050527</startdate><enddate>20050527</enddate><creator>Deschamps, Anne M</creator><creator>Apple, Kimberly A</creator><creator>Leonardi, Amy H</creator><creator>McLean, Julie E</creator><creator>Yarbrough, William M</creator><creator>Stroud, Robert E</creator><creator>Clark, Leslie L</creator><creator>Sample, Jeffrey A</creator><creator>Spinale, Francis G</creator><general>American Heart Association, Inc</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20050527</creationdate><title>Myocardial Interstitial Matrix Metalloproteinase Activity Is Altered by Mechanical Changes in LV Load: Interaction With the Angiotensin Type 1 Receptor</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4023-8a55d5bf377df8bd422c5620bb1b5973c4f11862d8e1a57ce12090ad35519e5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Angiotensin II Type 1 Receptor Blockers - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hypertension - enzymology</topic><topic>Hypertension - physiopathology</topic><topic>Intra-Aortic Balloon Pumping</topic><topic>Matrix Metalloproteinases - metabolism</topic><topic>Myocardium - enzymology</topic><topic>Receptor, Angiotensin, Type 1 - physiology</topic><topic>Swine</topic><topic>Ventricular Function, Left</topic><topic>Ventricular Remodeling</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deschamps, Anne M</creatorcontrib><creatorcontrib>Apple, Kimberly A</creatorcontrib><creatorcontrib>Leonardi, Amy H</creatorcontrib><creatorcontrib>McLean, Julie E</creatorcontrib><creatorcontrib>Yarbrough, William M</creatorcontrib><creatorcontrib>Stroud, Robert E</creatorcontrib><creatorcontrib>Clark, Leslie L</creatorcontrib><creatorcontrib>Sample, Jeffrey A</creatorcontrib><creatorcontrib>Spinale, Francis G</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deschamps, Anne M</au><au>Apple, Kimberly A</au><au>Leonardi, Amy H</au><au>McLean, Julie E</au><au>Yarbrough, William M</au><au>Stroud, Robert E</au><au>Clark, Leslie L</au><au>Sample, Jeffrey A</au><au>Spinale, Francis G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myocardial Interstitial Matrix Metalloproteinase Activity Is Altered by Mechanical Changes in LV Load: Interaction With the Angiotensin Type 1 Receptor</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2005-05-27</date><risdate>2005</risdate><volume>96</volume><issue>10</issue><spage>1110</spage><epage>1118</epage><pages>1110-1118</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>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<0.05). With IABP disengagement, segmental shortening (% change from baseline of 0) remained depressed in the vehicle group (-32.2±11.8%, P<0.05) but returned to baseline in the AT1RB group (2.3±12.5%). MMP activity decreased with IABP in both groups. At IABP disengagement, a surge in MMP activity occurred in the vehicle group that was abrogated with AT1RB (3.03±0.85 versus 0.07±1.55 MMP units/hr, P<0.05). A transient increase in LV load caused a cyclic variation in interstitial MMP activity that is regulated in part by the AT1R. These temporally dynamic changes in MMP activity likely influence myocardial function and structure with increased LV load.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>15860759</pmid><doi>10.1161/01.RES.0000167830.12010.6b</doi><tpages>9</tpages></addata></record> |
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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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