Document Detail


Effects of external wrapping and increased blood flow on atrophy of the baboon iliac artery.
MedLine Citation:
PMID:  18358668     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: Increased blood flow causes neointimal atrophy, whereas relief of wall tension with an external wrap causes arterial medial atrophy. To study the effects of blood flow and wall tension separately and together, we applied tight or loose wraps on high-flow or normal-flow iliac arteries in baboons. METHOD: Baboon external iliac arteries were wrapped with loose-fitting and tight-fitting expanded polytetrafluoroethylene (ePTFE), leaving part unwrapped. A downstream arteriovenous fistula was constructed on one side to increase blood flow approximately twofold. The arteries were perfusion-fixed with 10% formalin after 4 (n = 5) and 28 days (n = 5). RESULTS: At 4 days, compared with the unwrapped artery, the loosely and tightly wrapped normal-flow artery showed significant medial atrophy (23% and 30%, respectively; P < .05). The tightly wrapped artery showed a loss of cells (27%; P = .02) but no change in cell density. At 28 days, the medial cross-sectional area was decreased by the tight wrap and loose wrap under normal (45% and 28%, respectively; P < .05) and high (43% and 29%, respectively; P < .05) flow. High flow did not alter the effect of wrapping nor did it affect the unwrapped medial area. At 28 days, the normal and high flow tightly wrapped media showed an insignificant loss of cells but had increased cell density (47% and 30%, respectively; P < .05), suggesting preferential loss of extracellular matrix. Decorin was expressed at the late time only in the tightly wrapped normal and high-flow media and was associated with tight packing of the collagen, as detected by picrosirius red staining. CONCLUSION: Loose-fitting and tight-fitting ePTFE wraps induced an inflammatory foreign body response that caused medial atrophy with loss of cells and extracellular matrix; the tight wrap was more effective. High blood flow did not prevent or augment medial atrophy. CLINICAL RELEVANCE: Research in arterial restenosis has focused on the biologic mechanisms and pharmacologic approaches to the prevention of intimal hyperplasia. An alternative therapeutic approach might be to induce atrophy of established intimal hyperplasia. We have previously reported that high blood flow induces neointimal regression in expanded polytetrafluoroethylene grafts in baboons. Here we provide another model of vascular atrophy induced by external wrapping. The similarity between baboons and humans in their vascular systems and individual genetic heterogeneity makes these experiments of great relevance. Up- or down-regulated genes common to both models might be key regulators of vascular atrophy and therefore suitable therapeutic targets for pharmacologic treatment of established lesions.
Authors:
Seung-Kee Min; Richard D Kenagy; Joseph P Jeanette; Alexander W Clowes
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2008-03-21
Journal Detail:
Title:  Journal of vascular surgery : official publication, the Society for Vascular Surgery [and] International Society for Cardiovascular Surgery, North American Chapter     Volume:  47     ISSN:  0741-5214     ISO Abbreviation:  J. Vasc. Surg.     Publication Date:  2008 May 
Date Detail:
Created Date:  2008-05-05     Completed Date:  2008-06-12     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  8407742     Medline TA:  J Vasc Surg     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1039-47     Citation Subset:  IM    
Affiliation:
Department of Surgery, Seoul National University, Seoul, Korea.
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MeSH Terms
Descriptor/Qualifier:
Animals
Arteriovenous Shunt, Surgical*
Atrophy
Bandages / adverse effects*
Cell Death
Cell Proliferation
Equipment Design
Extracellular Matrix / metabolism
Femoral Artery / surgery
Femoral Vein / surgery
Foreign-Body Migration / etiology*,  metabolism,  pathology,  physiopathology
Iliac Artery* / metabolism,  pathology,  physiopathology
Male
Models, Animal
Papio
Polytetrafluoroethylene*
Pressure
Regional Blood Flow
Stress, Mechanical
Time Factors
Grant Support
ID/Acronym/Agency:
HL30946/HL/NHLBI NIH HHS; P51 RR000166-440158/RR/NCRR NIH HHS; P51 RR000166-455491/RR/NCRR NIH HHS; P51 RR000166-467611/RR/NCRR NIH HHS; R01 HL030946-22/HL/NHLBI NIH HHS; R01 HL030946-23/HL/NHLBI NIH HHS; R01 HL030946-24/HL/NHLBI NIH HHS; RR00166/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
9002-84-0/Polytetrafluoroethylene
Comments/Corrections

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