(Circulation. 2001;104:1538.)
© 2001 American Heart Association, Inc.
Basic Science Reports |
From the Department of Physiology and Pharmacology, University of Strathclyde, and Department of Pathology, Glasgow Royal Infirmary (A.R.M.), Glasgow, Scotland, UK. Dr Work is now at the Department of Medicine and Therapeutics, Western Infirmary, Glasgow.
Correspondence to Dr C.L. Wainwright, Department of Physiology and Pharmacology, University of Strathclyde, Strathclyde Institute for Biomedical Sciences, 27 Taylor St, Glasgow G4 0NR, Scotland, UK. E-mail c.l.wainwright{at}strath.ac.uk
Background Mitogenic stimuli present at the site of coronary arterial balloon injury contribute to the progression and development of a restenotic lesion, many signaling through a common pathway involving the small G protein p21ras. Our aim was to demonstrate in biochemical studies that farnesyl protein transferase inhibitor III (FPTIII) is an inhibitor of p21ras processing and that when it is given locally in vivo at the site of coronary balloon injury in a porcine model, it can inhibit neointima formation.
Methods and Results FPTIII (1 to 25 µmol/L) concentration-dependently reduced p21ras levels in porcine coronary artery smooth muscle cell membranes. FPTIII also prevented p42/p44 MAPK activation and DNA synthesis in response to platelet-derived growth factor in these cells at a concentration of 25 µmol/L. Application of 25 µmol/L FPTIII locally for 15 minutes to balloon-injured porcine coronary arteries in vivo prevented neointima formation assessed at 4 weeks, reduced proteoglycan deposition, and inhibited adventitial hypertrophy. Coronary arteries from FPTIII-treated pigs had no deterioration in contraction or in endothelium-dependent relaxation.
Conclusions The study demonstrates in the pig that short-term local delivery of inhibitors of p21ras-dependent mitogenic signal transduction prevents restenosis after balloon angioplasty.
Key Words: neointima farnesyl transferase inhibitor arteries angioplasty
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