2010
DOI: 10.1097/mca.0b013e328336e9f3
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Prolonged hypercholesterolemia-induced tissue factor expression in rabbit vein grafts: a potential mechanism for graft failure

Abstract: Prolonged expression of biologically active rabbit TF and TF protein were shown within jugular vein grafts of hypercholesterolemic rabbits. This response, reported for the first time and attributed to increased cholesterol levels, may possibly contribute to enhanced hyperplasia. These results suggest that TF expression could serve as another mechanism underlying vein graft failure and that hypercholesterolemia in bypass patients should be treated aggressively beginning within the weeks after surgery.

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Cited by 4 publications
(3 citation statements)
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References 23 publications
(31 reference statements)
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“…For example, graft failure due to thrombosis is a significant clinical problem and several studies implicate ectopic TF expression in response to hemodynamic changes as a driver of clot formation. [52][53][54] Our model suggests differential behaviors for the two TFs might inform specific and novel methods for modifying spontaneous thrombosis in the venous and arterial circulation.…”
Section: Plos Geneticsmentioning
confidence: 92%
“…For example, graft failure due to thrombosis is a significant clinical problem and several studies implicate ectopic TF expression in response to hemodynamic changes as a driver of clot formation. [52][53][54] Our model suggests differential behaviors for the two TFs might inform specific and novel methods for modifying spontaneous thrombosis in the venous and arterial circulation.…”
Section: Plos Geneticsmentioning
confidence: 92%
“…One recent strategy for dealing with venous graft failure involves a novel complex electro-spun external sheath which can slowly/gradually and time-dependently release loaded fasudil dihydrochloride, everolimus and simvastatin at the level of a vein graft [203]. The combined effect of mechanical restriction exerted by the sheath and loaded fasudil can alleviate the damage on the endothelial line and trigger endothelial repair through Rho/ROCK activation to prevent early phase graft failure [204,205]. Middle phase graft failure due to SMC proliferation is efficiently inhibited by the loaded everolimus.…”
Section: Current and Potential Therapeutic Usesmentioning
confidence: 99%
“…Blood cells and endothelial cells were directly contacted with the circulation, which do not express tissue factor in general condition. Many stimulating factors, such as bacterial endotoxin, tumor necrosis factor, and type oxidized low density lipoprotein (ox-LDL) attack vascular endothelial cells and monocytes to express TF [31,32]. Excessive expression of TF was closely related to the thrombosis of many diseases, such as sepsis, cancer and atherosclerosis [33].…”
Section: Discussionmentioning
confidence: 99%