EJCTS Click here for details of sales 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):
Munir Boodhwani
Shigetoshi Mieno
Basel Ramlawi
Frank W. Sellke
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Boodhwani, M.
Right arrow Articles by Sellke, F. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Boodhwani, M.
Right arrow Articles by Sellke, F. W.
Related Collections
Right arrow Cardiac - physiology
Right arrow Coronary disease
Right arrow Minimally invasive surgery
Right arrow Molecular biology

Eur J Cardiothorac Surg 2006;29:736-741
© 2006 Elsevier Science NL

Effects of purified poloxamer 407 gel on vascular occlusion and the coronary endothelium

Munir Boodhwani, Jun Feng, Shigetoshi Mieno, Basel Ramlawi, Neel Sodha, Richard Clements, Frank W. Sellke *

Division of Cardiothoracic Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, 110 Francis Street, LMOB 2A, Boston, MA 02215, United States

Received 30 August 2005; received in revised form 24 January 2006; accepted 9 February 2006.

* Corresponding author. Tel.: +1 617 632 8385; fax: +1 617 632 8387. (Email: fsellke{at}bidmc.harvard.edu).

Objective: Vascular occlusion during off-pump coronary surgery often results in sub-optimal visualization and endothelial damage of the target vessel. We have previously reported the safety of purified poloxamer 407, a gel with reverse thermosensitive properties, in a model of off-pump coronary occlusion. The aim of this study was to evaluate different gel concentrations and their effects on coronary occlusion time, myocardial contractility, endothelial function, and markers of myocardial injury and apoptosis. Methods: Yorkshire swine (30–35 kg) underwent sternotomy and mid-LAD occlusion using either microvascular clamps (n = 6) or varying quantities of three different concentrations (20%; n = 6, 22.5%; n = 3, and 25%; n = 3) of purified poloxamer 407 gel. Distal LAD flow, left ventricular pressure, and in vitro microvascular reactivity were assessed. Molecular markers of myocardial injury and apoptosis were assessed using Western blotting. Results: Duration of ischemia correlated significantly with the amount of injected gel for the 20% and 22.5% formulations (Spearman r = 0.64, p = 0.02 and r = 0.85, p = 0.03, respectively) but not for the 25% gel (r = 0.22, p = 0.66). There were no significant differences in LV contractility (maximum + dp/dt) (p = 0.86) as well as LAD flow (p = 0.25) during reperfusion in the four groups. Microvessel relaxation to adenosine diphosphate in the ischemic territory was impaired with higher concentrations of the gel, 22.5% (–14.8 ± 7.5% vs control at 10–5 mol/L, p < 0.05) and 25% gel (–24.0 ± 7.6% vs control at 10–5 mol/L, p < 0.001) but not with the 20% gel. Endothelium-independent relaxation to sodium nitroprusside was preserved in all groups. Cleaved poly(ADP-ribose) polymerase, a marker of myocardial injury and apoptosis, was elevated in the ischemic myocardium in all groups (p = 0.02 vs non-ischemic myocardium) with no significant differences between the groups (p = 0.70). Phosphorylation of Bad, an anti-apoptotic protein, was significantly reduced in the ischemic territory (p = 0.04). No changes were observed in other markers of myocardial apoptosis. Conclusions: Purified poloxamer 407 gel is effective for temporary coronary vascular occlusion. Coronary artery occlusion time is related to gel concentration and the quantity of gel injected. The higher gel concentrations may cause endothelial dysfunction of the distal vasculature and therefore should be avoided.

Key Words: Off-pump • Biomaterials • Endothelium • Coronary artery bypass grafts • CABG • Apoptosis







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 © 2006 European Association for Cardio-Thoracic Surgery. Published by Elsevier. All rights reserved.