Document Detail


Development of an in vitro system to assess stent-induced smooth muscle cell proliferation: a feasibility study.
MedLine Citation:
PMID:  19028120     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
PURPOSE: To develop an in vitro system capable of rapidly evaluating how specific stent structures may stimulate smooth muscle cell proliferation in living isolated porcine carotid arteries. MATERIALS AND METHODS: A vascular bioreactor system was developed that housed a native porcine carotid artery under physiologic pulsatile flow and pressure conditions. The bioreactor system was designed to enable vascular stent deployment into a test section of vessel that was kept alive for 1 week. The three stents tested were a Wallstent, a Cordis Smart stent, and a balloon-expandable NIR Royal stent in three different arteries. RESULTS: Stents were successfully deployed in the native porcine arteries within the bioreactor system. Organ bath studies demonstrated that the explanted arteries maintained 40% of their contractility. Immunohistochemical staining of the stented vessel demonstrated that smooth muscle cell proliferation was related to stent design and strut location. Specifically, smooth muscle proliferation was shown to increase with stiffer (less compliant) vascular stents and in the edge region of the stents. CONCLUSIONS: The system could potentially be used to assess the influence of stent design and smooth muscle cell proliferation.
Authors:
Saami K Yazdani; Joel L Berry
Publication Detail:
Type:  Journal Article     Date:  2008-11-22
Journal Detail:
Title:  Journal of vascular and interventional radiology : JVIR     Volume:  20     ISSN:  1535-7732     ISO Abbreviation:  J Vasc Interv Radiol     Publication Date:  2009 Jan 
Date Detail:
Created Date:  2008-12-26     Completed Date:  2009-02-05     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9203369     Medline TA:  J Vasc Interv Radiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  101-6     Citation Subset:  IM    
Affiliation:
Department of Biomedical Engineering, Virginia Tech - Wake Forest School of Biomedical Engineering and Sciences, Wake Forest University, Winston-Salem, NC 27157, USA. syazdani@wfubmc.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Bioreactors*
Blood Pressure
Carotid Artery Injuries / etiology,  pathology*,  physiopathology
Cell Proliferation*
Feasibility Studies
Hyperplasia
Immunohistochemistry
Materials Testing
Muscle, Smooth, Vascular / injuries,  pathology*
Myocytes, Smooth Muscle / pathology*
Prosthesis Design
Pulsatile Flow
Stents / adverse effects*
Stress, Mechanical
Swine
Time Factors
Tissue Culture Techniques*
Vasoconstriction

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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