Regression of pressure overload-induced left ventricular hypertrophy in mice

1 Experimental Cardiology Laboratory, Baker Heart Research Institute, and Alfred Heart Centre, Alfred Hospital, and 2 Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia Submitted 18 August 2004 ; accepted in final form 13 January 2005 As a prelude to investigating the mechanism of regress...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2005-06, Vol.288 (6), p.H2702-H2707
Hauptverfasser: Gao, Xiao-Ming, Kiriazis, Helen, Moore, Xiao-Lei, Feng, Xin-Heng, Sheppard, Karen, Dart, Anthony, Du, Xiao-Jun
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container_end_page H2707
container_issue 6
container_start_page H2702
container_title American journal of physiology. Heart and circulatory physiology
container_volume 288
creator Gao, Xiao-Ming
Kiriazis, Helen
Moore, Xiao-Lei
Feng, Xin-Heng
Sheppard, Karen
Dart, Anthony
Du, Xiao-Jun
description 1 Experimental Cardiology Laboratory, Baker Heart Research Institute, and Alfred Heart Centre, Alfred Hospital, and 2 Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia Submitted 18 August 2004 ; accepted in final form 13 January 2005 As a prelude to investigating the mechanism of regression of pressure overload-induced left ventricular (LV) hypertrophy (LVH), we studied the time course for the development and subsequent regression of LVH as well as accompanying alterations in cardiac function, histology, and gene expression. Mice were subjected to aortic banding for 4 or 8 wk to establish LVH, and regression was initiated by release of aortic banding for 6 wk. Progressive increase in LV mass and gradual chamber dilatation and dysfunction occurred after aortic banding. LVH was also associated with myocyte enlargement, interstitial fibrosis, and enhanced expression of atrial natriuretic peptide, collagen I, collagen III, and matrix metalloproteinase-2 but suppressed expression of -myosin heavy chain and sarcoplasmic reticulum Ca 2+ -ATPase. Aortic debanding completely or partially reversed LVH, chamber dilatation and dysfunction, myocyte size, interstitial fibrosis, and gene expression pattern, each with a distinct time course. The extent of LVH regression was dependent on the duration of pressure overload, evidenced by the fact that restoration of LV structure and function was complete in animals subjected to 4 wk of aortic banding but incomplete in animals subjected to 8 wk of aortic banding. In conclusion, LVH regression comprises a variety of morphological, functional, and genetic components that show distinct time courses. A longer period of pressure overload is associated with a slower rate of LVH regression. aortic banding; cardiac function/remodeling; model Address for reprint requests and other correspondence: X.-J. Du, Baker Heart Research Institute, PO Box 6492, St. Kilda Rd. Central, Melbourne, Victoria 8008, Australia (E-mail: xiaojun.du{at}baker.edu.au )
doi_str_mv 10.1152/ajpheart.00836.2004
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Mice were subjected to aortic banding for 4 or 8 wk to establish LVH, and regression was initiated by release of aortic banding for 6 wk. Progressive increase in LV mass and gradual chamber dilatation and dysfunction occurred after aortic banding. LVH was also associated with myocyte enlargement, interstitial fibrosis, and enhanced expression of atrial natriuretic peptide, collagen I, collagen III, and matrix metalloproteinase-2 but suppressed expression of -myosin heavy chain and sarcoplasmic reticulum Ca 2+ -ATPase. Aortic debanding completely or partially reversed LVH, chamber dilatation and dysfunction, myocyte size, interstitial fibrosis, and gene expression pattern, each with a distinct time course. The extent of LVH regression was dependent on the duration of pressure overload, evidenced by the fact that restoration of LV structure and function was complete in animals subjected to 4 wk of aortic banding but incomplete in animals subjected to 8 wk of aortic banding. 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Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>288</volume><issue>6</issue><spage>H2702</spage><epage>H2707</epage><pages>H2702-H2707</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>1 Experimental Cardiology Laboratory, Baker Heart Research Institute, and Alfred Heart Centre, Alfred Hospital, and 2 Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia Submitted 18 August 2004 ; accepted in final form 13 January 2005 As a prelude to investigating the mechanism of regression of pressure overload-induced left ventricular (LV) hypertrophy (LVH), we studied the time course for the development and subsequent regression of LVH as well as accompanying alterations in cardiac function, histology, and gene expression. Mice were subjected to aortic banding for 4 or 8 wk to establish LVH, and regression was initiated by release of aortic banding for 6 wk. 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A longer period of pressure overload is associated with a slower rate of LVH regression. aortic banding; cardiac function/remodeling; model Address for reprint requests and other correspondence: X.-J. Du, Baker Heart Research Institute, PO Box 6492, St. Kilda Rd. Central, Melbourne, Victoria 8008, Australia (E-mail: xiaojun.du{at}baker.edu.au )</abstract><cop>United States</cop><pmid>15665058</pmid><doi>10.1152/ajpheart.00836.2004</doi><oa>free_for_read</oa></addata></record>
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subjects Animals
Atrial Natriuretic Factor - genetics
Calcium-Transporting ATPases - genetics
Collagen - genetics
Disease Models, Animal
DNA Primers
Echocardiography
Female
Hypertrophy, Left Ventricular - diagnostic imaging
Hypertrophy, Left Ventricular - etiology
Hypertrophy, Left Ventricular - physiopathology
Male
Matrix Metalloproteinases - genetics
Mice
Mice, Inbred C57BL
Pressure
Reverse Transcriptase Polymerase Chain Reaction
Sarcoplasmic Reticulum Calcium-Transporting ATPases
Ventricular Pressure - physiology
Ventricular Remodeling - physiology
title Regression of pressure overload-induced left ventricular hypertrophy in mice
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