Vascular injury, repair, and restenosis after percutaneous transluminal angioplasty in the atherosclerotic rabbit.

BACKGROUND Several nonatherosclerotic animal models of restenosis exist and are used for the evaluation of the vascular response to angioplasty-induced injury. However, few studies have evaluated the response of an atherosclerotic vessel to angioplasty. The present study examined the radiographic, histological, immunohistochemical, and morphometric responses over time of atherosclerotic rabbit femoral arteries after percutaneous transluminal angioplasty (PTA). METHODS AND RESULTS Rabbits (n = 94) underwent arterial dissection and were fed a hypercholesterolemic diet for 3 weeks, and then PTA was performed. Arteries were obtained before PTA and 1, 3, 5, 7, 14, and 28 days after PTA. PTA caused radial stretching of the artery, medial compression, intramural hemorrhage, injury to normal arterial segments, and dissection within the intima and media. Thrombus filled and cellular accumulation repaired the dissection. Peak smooth muscle cell and macrophage DNA synthesis was noted at 3 to 5 days after angioplasty, generally at the dissection but also in normal sections of the artery. Adventitial injury and subsequent adventitial cellular proliferation and collagen production were observed. A rapid decrease in the radiographic minimal luminal diameter was noted at 3 days, resulting from vascular recoil or thrombus filling the dissection. At 7 to 14 days, only 24% to 33% of the luminal loss was accounted for by an increase in the intimal area, and 22% to 28% of the intima was neointima. CONCLUSIONS Restenosis in an atherosclerotic artery results from a variable combination of intimal proliferation, vascular remodeling/wound contraction, and recoil of the normal section of the artery. The variability of an atherosclerotic artery to PTA injury results from variable dissection, thrombus formation, and cellular response to injury as well as variable scar contraction and elastic recoil.

[1]  T. Hoshino,et al.  Significance of intimal tears in the mechanism of luminal enlargement in percutaneous transluminal coronary angioplasty: correlation of histologic and angiographic findings in postmortem human hearts. , 1987, American heart journal.

[2]  P. Douek,et al.  Rabbit ear model of injury-induced arterial smooth muscle cell proliferation. Kinetics, reproducibility, and implications. , 1991, Circulation research.

[3]  T. Ryan,et al.  Acute Effects of Transluminal Angioplasty in Three Experimental Models of Atherosclerosis , 1982, Arteriosclerosis.

[4]  M. Nobuyoshi,et al.  Restenosis after successful percutaneous transluminal coronary angioplasty: serial angiographic follow-up of 229 patients. , 1988, Journal of the American College of Cardiology.

[5]  M. Stepp,et al.  Complex regulation of collagen gene expression in cultured bovine aortic smooth muscle cells. , 1986, The Journal of biological chemistry.

[6]  A. Gown,et al.  HHF35, a muscle actin-specific monoclonal antibody. II. Reactivity in normal, reactive, and neoplastic human tissues. , 1987, The American journal of pathology.

[7]  T. Ryan,et al.  Differences in compensatory vessel enlargement, not intimal formation, account for restenosis after angioplasty in the hypercholesterolemic rabbit model. , 1994, Circulation.

[8]  J. Tobis,et al.  Morphological Effects of Coronary Balloon Angioplasty In Vivo Assessed by Intravascular Ultrasound Imaging , 1992, Circulation.

[9]  C. Haudenschild,et al.  Influence of inflation pressure and balloon size on the development of intimal hyperplasia after balloon angioplasty. A study in the atherosclerotic rabbit. , 1989, Circulation.

[10]  G. Wolf,et al.  New rabbit atherosclerosis model for the investigation of transluminal angioplasty. , 1981, Investigative radiology.

[11]  B. Hammill,et al.  Flecainide for supraventricular tachycardia in children. , 1988, The American journal of cardiology.

[12]  M. Nobuyoshi,et al.  Restenosis after percutaneous transluminal coronary angioplasty: pathologic observations in 20 patients. , 1991, Journal of the American College of Cardiology.

[13]  G. D. De Meyer,et al.  The endothelium during cuff-induced neointima formation in the rabbit carotid artery. , 1993, Arteriosclerosis and thrombosis : a journal of vascular biology.

[14]  Julie H. Campbell,et al.  Collagen synthesis by cultured rabbit aortic smooth-muscle cells. Alteration with phenotype. , 1990, The Biochemical journal.

[15]  W. Roberts,et al.  Effects of percutaneous transluminal coronary angioplasty on atherosclerotic plaques and relation of plaque composition and arterial size to outcome. , 1988, The American journal of cardiology.

[16]  A. Gown,et al.  Immunocytochemical analysis of cellular components in atherosclerotic lesions. Use of monoclonal antibodies with the Watanabe and fat-fed rabbit. , 1986, Arteriosclerosis.

[17]  R. Virmani,et al.  Plaque morphology and pathologic changes in arteries from patients dying after coronary balloon angioplasty. , 1990, Journal of the American College of Cardiology.

[18]  S. Hsu,et al.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[19]  E J Topol,et al.  Experimental models of coronary artery restenosis. , 1992, Journal of the American College of Cardiology.

[20]  W. Schürch,et al.  Myofibroblasts from diverse pathologic settings are heterogeneous in their content of actin isoforms and intermediate filament proteins. , 1989, Laboratory investigation; a journal of technical methods and pathology.

[21]  R. Kuntz,et al.  The relative importance of arterial remodeling compared with intimal hyperplasia in lumen renarrowing after balloon angioplasty. A study in the normal rabbit and the hypercholesterolemic Yucatan micropig. , 1994, Circulation.

[22]  D. Hathaway,et al.  Effects of thiol protease inhibitors on cell cycle and proliferation of vascular smooth muscle cells in culture. , 1993, Circulation research.

[23]  M. Reidy,et al.  Mechanisms of stenosis after arterial injury. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[24]  J. Isner,et al.  How Does Angioplasy Work?: Serial Analysis of Human Iliac Arteries Using Intravascular Ultrasound , 1992, Circulation.

[25]  D. Herrington,et al.  Qualitative and quantitative contrasts in the mechanisms of lumen enlargement by coronary balloon angioplasty and directional coronary atherectomy. , 1994, Journal of the American College of Cardiology.

[26]  P. Armstrong,et al.  Extracellular matrix remodeling after balloon angioplasty injury in a rabbit model of restenosis. , 1994, Circulation research.

[27]  P W Serruys,et al.  Incidence of restenosis after successful coronary angioplasty: a time-related phenomenon. A quantitative angiographic study in 342 consecutive patients at 1, 2, 3, and 4 months. , 1988, Circulation.

[28]  K. Karsch,et al.  Time course of smooth muscle cell proliferation in the intima and media of arteries following experimental angioplasty. , 1990, Circulation research.

[29]  G. Liau,et al.  Regulation of extracellular matrix RNA levels in cultured smooth muscle cells. Relationship to cellular quiescence. , 1989, The Journal of biological chemistry.