Physiol. Genomics Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Physiol. Genomics 9: 49-56, 2002; doi:10.1152/physiolgenomics.00035.2001
1094-8341/02 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (16)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Del Monte, F.
Right arrow Articles by Hajjar, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Del Monte, F.
Right arrow Articles by Hajjar, R. J.
Received 9 May 2001; accepted in final form 25 February 2002.
Physiological Genomics 9:49-56 (2002)
1094-8341/02 $5.00 © 2002 American Physiological Society

Novel technique of aortic banding followed by gene transfer during hypertrophy and heart failure

Federica Del Monte1,2,3, Karyn Butler4, Wolfgang Boecker1, Judith K. Gwathmey2,3 and Roger J. Hajjar1,2

1 Program in Cardiovascular Gene Therapy, Cardiovascular Research Center, Massachusetts General Hospital
2 Harvard Medical School, Boston
3 Gwathmey Inc., Cambridge, Massachusetts
4 Morehouse School of Medicine, Department of Surgery, Atlanta, Georgia

Aortic banding in the rat has become a popular method to induce left ventricular (LV) hypertrophy and heart failure. However, because of often extensive intrathoracic adhesions and inflammatory cell infiltrates resulting from the traditional surgical approach, an uncomplicated second thoracic incision for genetic manipulation is impeded. In this study, we describe a novel surgical technique of aortic banding which avoids opening the sternum and thereby avoids adhesions and surgery-related inflammation. Placing a clip on the ascending aorta using a suprasternal approach in Sprague-Dawley rats created proximal aortic constriction. The present study was initiated to determine whether a replication-deficient adenovirus would enable efficient gene transfer to adult cardiac myocytes undergoing hypertrophy and transitioning to heart failure. Echocardiography performed at week 24 revealed significant concentric hypertrophy and increased fractional shortening followed by LV dilatation with decreased fractional shortening after 27 wk of banding. An adenoviral solution encoding for the reporter green fluorescent protein gene (GFP) was delivered to the heart. Fluorescent microscopy revealed global gene expression throughout hypertrophied and failing hearts. Our studies demonstrate that a novel suprasternal approach can be applied to create an LV hypertrophy model followed by heart failure which also allows investigators to perform genetic manipulations in vivo through gene transfer without the complication of adhesions and surgical trauma-induced inflammation. Furthermore, our approach to delivery of transgenes results in homogenous gene expression in both hypertrophied and failing hearts.

cardiac; gene therapy; rats




This article has been cited by other articles:


Home page
Circ. Res.Home page
E. Cingolani, G. A. Ramirez Correa, E. Kizana, M. Murata, H. C. Cho, and E. Marban
Gene Therapy to Inhibit the Calcium Channel {beta} Subunit: Physiological Consequences and Pathophysiological Effects in Models of Cardiac Hypertrophy
Circ. Res., July 20, 2007; 101(2): 166 - 175.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
H. Yin, L. Chao, and J. Chao
Kallikrein/Kinin Protects against Myocardial Apoptosis after Ischemia/Reperfusion via Akt-Glycogen Synthase Kinase-3 and Akt-Bad{middle dot}14-3-3 Signaling Pathways
J. Biol. Chem., March 4, 2005; 280(9): 8022 - 8030.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
D. Lebeche, R. Kaprielian, F. del Monte, G. Tomaselli, J. K. Gwathmey, A. Schwartz, and R. J. Hajjar
In Vivo Cardiac Gene Transfer of Kv4.3 Abrogates the Hypertrophic Response in Rats After Aortic Stenosis
Circulation, November 30, 2004; 110(22): 3435 - 3443.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
Y. Li, T. Ha, X. Gao, J. Kelley, D. L. Williams, I. W. Browder, R. L. Kao, and C. Li
NF-{kappa}B activation is required for the development of cardiac hypertrophy in vivo
Am J Physiol Heart Circ Physiol, October 1, 2004; 287(4): H1712 - H1720.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
H. Yin, L. Chao, and J. Chao
Adrenomedullin Protects Against Myocardial Apoptosis After Ischemia/Reperfusion Through Activation of Akt-GSK Signaling
Hypertension, January 1, 2004; 43(1): 109 - 116.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
S. R. Houser and K. B. Margulies
Is Depressed Myocyte Contractility Centrally Involved in Heart Failure?
Circ. Res., March 7, 2003; 92(4): 350 - 358.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online