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Effect of Controlled Adventitial Heparin Delivery on Smooth Muscle Cell Proliferation Following Endothelial Injury

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Specialty Science
Date 1990 May 1
PMID 2339120
Citations 33
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Abstract

Continuous intravenous infusion of heparin suppresses smooth muscle cell proliferation in rats after endothelial injury but may lead to hemorrhage and other complications. The anticoagulant property has been removed from chemically modified heparin without loss of antiproliferative effect but use of such compounds is still limited. In this study ethylene-vinyl acetate copolymer matrices containing standard and modified heparin were placed adjacent to rat carotid arteries at the time of balloon dendothelialization. After 14 days arterial occlusion by smooth muscle cell proliferation was defined. Matrix delivery of both heparin compounds effectively diminished this proliferation in comparison to controls without producing systemic anticoagulation or side effects. In addition, this mode of therapy appeared more effective than the administration of the same agents by either intravenous pumps or heparin/polymer matrices placed in a subcutaneous site distant from the injured carotid artery. Thus, heparin's inhibition of smooth muscle cell proliferation after vascular injury might be most effective within the microenvironment of the injured vessel wall, and the accelerated atherosclerosis or restenosis that often follows angioplasty and other vascular interventions might best be treated with site-specific therapy.

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References
1.
Stemerman M, Ross R . Experimental arteriosclerosis. I. Fibrous plaque formation in primates, an electron microscope study. J Exp Med. 1972; 136(4):769-89. PMC: 2139284. DOI: 10.1084/jem.136.4.769. View

2.
Powell J, Clozel J, Muller R, Kuhn H, Hefti F, Hosang M . Inhibitors of angiotensin-converting enzyme prevent myointimal proliferation after vascular injury. Science. 1989; 245(4914):186-8. DOI: 10.1126/science.2526370. View

3.
Clowes A, Karnowsky M . Suppression by heparin of smooth muscle cell proliferation in injured arteries. Nature. 1977; 265(5595):625-6. DOI: 10.1038/265625a0. View

4.
Guyton J, Rosenberg R, Clowes A, Karnovsky M . Inhibition of rat arterial smooth muscle cell proliferation by heparin. In vivo studies with anticoagulant and nonanticoagulant heparin. Circ Res. 1980; 46(5):625-34. DOI: 10.1161/01.res.46.5.625. View

5.
Somogyi P, Takagi H . A note on the use of picric acid-paraformaldehyde-glutaraldehyde fixative for correlated light and electron microscopic immunocytochemistry. Neuroscience. 1982; 7(7):1779-83. DOI: 10.1016/0306-4522(82)90035-5. View