Frequency and severity of cyclic flow alternations and platelet aggregation predict the severity of neointimal proliferation following experimental coronary stenosis and endothelial injury.
- 1 December 1991
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 88 (23) , 10624-10628
- https://doi.org/10.1073/pnas.88.23.10624
Abstract
The role of recurrent platelet aggregation in the development of neointimal proliferation of coronary arteries was explored in this study, and the hypothesis was evaluated that recurrent platelet aggregation and the consequent frequency and severity of cyclic coronary blood flow variations are important pathophysiologic factors in the subsequent development of neointimal proliferation. In 24 chronically instrumented dogs, variable degrees of coronary artery neointimal proliferation were observed 3 weeks after mechanical injury of the arterial endothelium and the placement of an external coronary artery constrictor. The severity of neointimal proliferation at 21 days was closely related to the frequency and severity of cyclic coronary blood flow variations during the initial 7 days after instrumentation of the animals, itself a manifestation of recurrent platelet aggregation and dislodgement. Pharmacological therapy with a dual thromboxane A2 synthetase inhibitor and receptor antagonist and with a serotonin S2 receptor antagonist frequently was successful in abolishing cyclic blood flow variations and in retarding neointimal proliferation.Keywords
This publication has 36 references indexed in Scilit:
- Local platelet activation causes vasoconstriction of large epicardial canine coronary arteries in vivo. Thromboxane A2 and serotonin are possible mediators.Circulation, 1989
- Effect of thromboxane and serotonin receptor antagonists on intracoronary platelet deposition in dogs with experimentally stenosed coronary arteries.Circulation, 1988
- Platelet-derived growth factor mRNA detection in human atherosclerotic plaques by in situ hybridization.Journal of Clinical Investigation, 1988
- Localization of T lymphocytes and macrophages in fibrous and complicated human atherosclerotic plaquesAtherosclerosis, 1988
- ENDOTHELIAL REGENERATION .8. INTERACTION OF SMOOTH-MUSCLE CELLS WITH ENDOTHELIAL REGROWTH1988
- Angiotensin II induces hypertrophy, not hyperplasia, of cultured rat aortic smooth muscle cells.Circulation Research, 1988
- Mechanisms of Arterial Graft Failure: The Role of Cellular ProliferationAnnals of the New York Academy of Sciences, 1987
- EFFECTS OF GROWTH-FACTORS INVIVO .1. CELL INGROWTH INTO POROUS SUBCUTANEOUS CHAMBERS1987
- Cooperative mediation by serotonin S2 and thromboxane A2/prostaglandin H2 receptor activation of cyclic flow variations in dogs with severe coronary artery stenoses.Circulation, 1987
- Thrombin‐Cellular InteractionsAnnals of the New York Academy of Sciences, 1986