Time course of smooth muscle cell proliferation in the intima and media of arteries following experimental angioplasty.
- 1 September 1990
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 67 (3) , 651-659
- https://doi.org/10.1161/01.res.67.3.651
Abstract
Smooth muscle cell (SMC) proliferation is known to be an important factor for the development of restenosis after percutaneous transluminal coronary angioplasty. To determine the time course of intimal and medial SMC proliferation and morphological changes after experimental angioplasty, an intimal atheroma was produced with repeated weak electrical stimulations in the right carotid artery of 45 male New Zealand White rabbits. Angioplasty was subsequently performed in 35 rabbits, and the proliferative responses were analyzed with histomorphological and immunohistological criteria at 3, 7, 14, 21, 28, and 42 days after intervention. A hemodynamic relevant stenosis after angioplasty was found in eight (23%) of 35 dilated arteries. In five rabbits the stenosis was due to a mural thrombus, and in three animals restenosis was caused by intimal SMC proliferation. In all dilated arteries the intimal wall thickness increased from 13 .+-. 5 intimal cell layers (after electrical stimulation) to 33 .+-. 14 cell layers during 28 days after angioplasty (p < 0.05). Later than 4 weeks after angioplasty, no additional increase of intimal thickening occurred. Application of bromodeoxyuridine 18 and 12 hours before excision of the vessels allowed determination of the percent of cells undergoing DNA synthesis in the intima and media using monoclonal antibody against bromodeoxyuridine. SMCs were identified by .alpha.-actin staining. Immunohistological quantification of intimal SMC proliferation showed a maximum of cells undergoing DNA synthesis within the first 7 days after angioplasty (p < 0.01). In contrast, medial proliferation of SMCs was delayed and showed a small but significant increase 21 days after dilatation (p < 0.05). Twenty-eight days after angioplasty, SMC proliferation in the media as well as in the intima was normalized and comparable to the control group without angioplasty.This publication has 39 references indexed in Scilit:
- Densitometric measurement of increased endothelial permeability in arteriosclerotic plaques and inhibition of permeability under the influence of two calcium antagonistsAtherosclerosis, 1989
- Re-Stenosis after Successful Coronary AngioplastyNew England Journal of Medicine, 1988
- Temporal sequence of morphological alterations in artery walls during experimental atherogenesis — occurrence of leukocytesZeitschrift für Die Gesamte Experimentelle Medizin, 1987
- The Pathogenesis of Atherosclerosis — An UpdateNew England Journal of Medicine, 1986
- Intimal proliferation of smooth muscle cells as an explanation for recurrent coronary artery stenosis after percutaneous transluminal coronary angioplastyJournal of the American College of Cardiology, 1985
- Inhibition of smooth muscle cell proliferation and endothelial permeability with flunarizine in vitro and in experimental atheromasZeitschrift für Die Gesamte Experimentelle Medizin, 1985
- Restenosis after percutaneous transluminal coronary angioplasty (PTCA): A report from the PTCA registry of the national heart, lung, and blood instituteThe American Journal of Cardiology, 1984
- Morphology after Transluminal Angioplasty in Human BeingsNew England Journal of Medicine, 1981
- Scanning electron microscopy after coronary transluminal angioplasty of normal canine coronary arteriesThe American Journal of Cardiology, 1980
- Responses of vessel walls to chronically applied electrical stimuliBasic Research in Cardiology, 1979