EJCTS Click here to locate an Ethicon representative
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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 PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Friedhelm Beyersdorf
Georg Lutter
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Heilmann, C.
Right arrow Articles by Lutter, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Heilmann, C.
Right arrow Articles by Lutter, G.
Related Collections
Right arrow Cardiac - other
Right arrow Coronary disease
Right arrow Molecular biology

Eur J Cardiothorac Surg 2002;22:957-964
© 2002 Elsevier Science NL


Comparison of protein with DNA therapy for chronic myocardial ischemia using fibroblast growth factor-2

Claudia Heilmanna, Patrick von Samsona, Kerstin Schlegela, Tim Attmanna, Bernd-Ulrich von Spechtb, Friedhelm Beyersdorfa, Georg Luttera*

a Department of Cardiovascular Surgery, Albert-Ludwigs-University Freiburg, Freiburg, Germany
b Department of Surgical Research, Albert-Ludwigs-University Freiburg, Freiburg, Germany

Received 5 May 2002; received in revised form 2 September 2002; accepted 4 September 2002.

* Corresponding author. Tel.: +49-761-270-2818; fax: +49-761-270-2550
e-mail: lutter{at}ch11.ukl.uni-freiburg.de

Objective: Treatment of coronary disease by growth factors has become an increasingly used strategy for otherwise untreatable patients and is subject to a number of clinical studies. The aim is to stimulate the development of a sufficient collateral circulation and hereby to rescue cardiac function. The objective of our study was to compare the effectiveness of fibroblast growth factor-2 (FGF-2) as protein and as naked plasmid DNA in a porcine model of chronic myocardial ischemia. Materials and methods: A severe stenosis of the left anterior descending artery (LAD) artery was created in healthy pigs. After 1 week, perfusion and regional and global contractility was assessed at baseline at rest and under stress. Afterwards, recombinant FGF-2 (n=6) or naked plasmid DNA encoding FGF-2 (n=7) was intramyocardially injected into the LAD territory. Control animals were left untreated (n=5). After 3 months, the animals were re-examined and underwent immunohistologic analysis. One animal received an Enhanced Green Fluorescent Protein plasmid. Results: Plasmid-dependent protein synthesis was present in cardiomyocytes. FGF-2 protein as well as plasmid injections resulted in an increased number of capillaries and of arterioles compared with untreated ischemia. The improvement of the regional myocardial blood flow by FGF-2 plasmid therapy at rest might however indicate the effectiveness of the DNA application for the induction of a collateral circulation. A benefit from FGF-2 plasmid therapy was revealed with regard to regional contractility. Systemic hemodynamics were partially improved following plasFGF-2 treatment. Conclusions: In this porcine model of chronic myocardial ischemia, intramyocardial injection of FGF-2 plasmid was more effective than of FGF-2 protein in improving regional perfusion and contractility compared to untreated ischemia.

Key Words: Coronary disease • Fibroblast growth factor-2 • Gene expression • Angiogenesis • Perfusion • Contractility




This article has been cited by other articles:


Home page
Eur. J. Cardiothorac. Surg.Home page
C. Heilmann and F. Beyersdorf
Editorial comment Growth factor therapy grows, despite limited insight.
Eur. J. Cardiothorac. Surg., July 1, 2006; 30(1): 107 - 108.
[Full Text] [PDF]


Home page
Exp PhysiolHome page
R. Morishita, M. Aoki, and T. Ogihara
Does gene therapy become pharmacotherapy?
Exp Physiol, May 1, 2005; 90(3): 307 - 313.
[Abstract] [Full Text] [PDF]


Home page
Eur. J. Cardiothorac. Surg.Home page
C. A.U. Heilmann, T. Attmann, A. Thiem, E. Haffner, F. Beyersdorf, and G. Lutter
Gene therapy in cardiac surgery: intramyocardial injection of naked plasmid DNA for chronic myocardial ischemia
Eur. J. Cardiothorac. Surg., November 1, 2003; 24(5): 785 - 793.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS
Copyright © 2002 European Association for Cardio-Thoracic Surgery. Published by Elsevier. All rights reserved.