Advertisement






Click here for more guidelines.
CME Topic Collections Past Issues Search Current Issue Home
     

J Am Coll Cardiol, 2001; 38:1570-1576
© 2001 by the American College of Cardiology Foundation
This Article
Right arrow Abstract Freely available
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
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 Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chandrasekar, B.
Right arrow Articles by Tanguay, J.-F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chandrasekar, B.
Right arrow Articles by Tanguay, J.-F.

Coronary artery endothelial protection after local delivery of 17ß-estradiol during balloon angioplasty in a porcine model: a potential new pharmacologic approach to improve endothelial function

Baskaran Chandrasekar, MD*, Stanley Nattel, MD, FACC* {dagger} and Jean-François Tanguay, MD, FACC*,*

* Department of Medicine, Montreal Heart Institute and University of Montreal, Montreal, Canada
{dagger} Department of Pharmacology and Therapeutics, McGill University, Montreal, Canada



View larger version (101K):

[in a new window]
 
Figure 1 Representative coronary angiograms demonstrating the vasoconstrictive response to intracoronary infusion of acetylcholine (Ach) 10–4 mol/l obtained from the same animal. Column A = basal, column B = post-Ach, column C = after nitroglycerin. Top = percutaneous transluminal coronary angioplasty (PTCA) plus vehicle, Middle = PTCA alone, Lower = PTCA plus 17ß-estradiol groups, respectively. Arrows = PTCA sites.

 


View larger version (14K):

[in a new window]
 
Figure 2 Graph showing the response of the three treatment groups to acetylcholine (Ach). Comparison for each treatment group is made between the basal coronary-artery diameter and diameter at the end of 10–7 mol/l, 10–6 mol/l, 10–5 mol/l and 10–4 mol/l Ach, respectively. Nitro = nitroglycerin; PTCA = percutaneous transluminal coronary angioplasty. *p = 0.01; **p < 0.0001; ***p = 0.02; ****p = 0.001.

 


View larger version (56K):

[in a new window]
 
Figure 3 Immunohistochemistry for re-endothelialization (A) and endothelial nitric oxide synthase (eNOS) expression (B) from a representative animal. Top (x40): (a) percutaneous transluminal coronary angioplasty (PTCA) plus 17ß-estradiol, (b) PTCA alone and (c) PTCA plus vehicle. Lower: portions of the cross sections are shown under high-power (x1,000, d to f, respectively) to highlight positive-staining luminal border. The length of positive staining in the high-power image is indicated by "RE" and "EN" immediately above each image, with the total luminal length in the image (T) shown above. This analysis was applied to the entire luminal surface, with percentage of re-endothelialization (RE) calculated as {Sigma}RE/{Sigma}T, where {Sigma}RE and {Sigma}T are the sums of re-endothelialized segment and total luminal lengths in each image. The extent of re-endothelialization for the cross section is greater in (a) (90%) than it is in (b) (65.8%) and (c) (66.1). Similar analysis was performed for percentage of eNOS expression (EN).

 




 
  CME Topic Collections Past Issues Search Current Issue Home

Advertisement