Skip Navigation

European Heart Journal 2001 22(14):1205-1213; doi:10.1053/euhj.2000.2446
Copyright © 2001 by the European Society of Cardiology.
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow References
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (12)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Belardinelli, R
Right arrow Articles by Shryock, J.C
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Belardinelli, R
Right arrow Articles by Shryock, J.C
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Effects of dipyridamole on coronary collateralization and myocardial perfusion in patients with ischaemic cardiomyopathy

R Belardinellia,f1, L Belardinellib and J.C Shryockb

a Servizio di Cardiologia Riabilitativa, Azienda Ospedaliera ‘G.M.Lancisi’ Ancona, Italy
b Department of Medicine, University of Gainesville, Florida, U.S.A.

revised August 31, 2000; accepted September 6, 2000

Abstract

Aims There is evidence that oral dipyridamole, a nucleoside uptake blocker that increases myocardial adenosine levels, lessens myocardial ischaemia by inducing coronary collateral growth in animal models of ischaemic heart disease. However, whether dipyridamole can exert a similar effect in humans with coronary artery disease is controversial.

Methods and Results We studied 30 male patients (mean age 55±9 years) with coronary artery disease and left ventricular systolic dysfunction (ejection fraction >40%). Patients were randomized into three matched groups. Group A patients (n=10) received dipyridamole alone at a dose of 75mg t.i.d. orally for 8 weeks. Group B patients (n=10) underwent exercise training at 60% of peak O2three times a week for 8 weeks, and received dipyridamole. Group C patients (n=10) had neither exercise testing nor dipyridamole. On study entry and after 8 weeks all patients underwent an exercise test with gas exchange analysis, dobutamine stress echocardiography, 201-thallium planar myocardial scintigraphy, and coronary angiography. Peak O2increased significantly only in trained patients. Thallium uptake of the collateral-dependent myocardium, coronary collateral score and wall thickening score increased significantly only in groups receiving dipyridamole, the greatest improvement being in group B patients. Plasma adenosine levels were also the highest in group B (P<0·001 vs A and C). Correlations were found between changes in adenosine levels and increases of both thallium uptake (r=–0·70;P=0·001) and collateralization (r=0·72;P=0·001).

Conclusion Exercise training potentiates the effects of dipyridamole on coronary collateralization and myocardial perfusion in humans with ischaemic cardiomyopathy.

Key Words: Dipyridamole, adenosine, myocardial scintigraphy, ischaemic heart disease

f1 Correspondence: Romualdo Belardinelli, MD, Via Rismondo, 5, 60100 Ancona, Italy.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
HeartHome page
S H Schirmer, F C van Nooijen, J J Piek, and N van Royen
Stimulation of collateral artery growth: travelling further down the road to clinical application
Heart, February 1, 2009; 95(3): 191 - 197.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
T. H. Adair
Growth regulation of the vascular system: an emerging role for adenosine
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2005; 289(2): R283 - R296.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
I. Shuralyova, P. Tajmir, P. J. Bilan, G. Sweeney, and I. R. Coe
Inhibition of glucose uptake in murine cardiomyocyte cell line HL-1 by cardioprotective drugs dilazep and dipyridamole
Am J Physiol Heart Circ Physiol, February 1, 2004; 286(2): H627 - H632.
[Abstract] [Full Text] [PDF]


Home page
Eur Heart JHome page
E. Picano and on behalf of the PISA study group
Dipyridamole in chronic stable angina pectoris. A randomized, double blind, placebo-controlled, parallel group study
Eur. Heart J., October 1, 2001; 22(19): 1785 - 1793.
[Abstract] [PDF]


Home page
Eur Heart JHome page
F. Lombardi and R. Rambaldi
Coronary angiogenesis: dipyridamole is back on the stage?
Eur. Heart J., July 2, 2001; 22(14): 1151 - 1153.
[PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.