YC-1-mediated vascular protection through inhibition of smooth muscle cell proliferation and platelet function.

Abstract

YC-1, a synthetic benzyl indazole derivative, is capable of stimulating endogenous vessel wall cyclic guanosine monophosphate (cGMP) production and attenuating the remodeling response to experimental arterial angioplasty. In an effort to investigate the mechanisms of this YC-1-mediated vasoprotection, we examined the influence of soluble YC-1 or YC-1 incorporated in a polyethylene glycol (PEG) hydrogel on cultured rat vascular smooth muscle cell (SMC) cGMP synthesis, SMC proliferation, and platelet function. Results demonstrate that soluble YC-1 stimulated SMC cGMP production in a dose-dependent fashion, while both soluble and hydrogel-released YC-1 inhibited vascular SMC proliferation in a dose-dependent fashion without effects on cell viability. Platelet aggregation and adherence to collagen were both significantly inhibited in a dose-dependent fashion by soluble and hydrogel-released YC-1. Arterial neointima formation following experimental balloon injury was significantly attenuated by perivascular hydrogel-released YC-1. These results suggest that YC-1 is a potent, physiologically active agent with major anti-proliferative and anti-platelet properties that may provide protection against vascular injury through cGMP-dependent mechanisms.

• Authors: David A Tulis, Kristyn S Bohl Masters, Elizabeth A Lipke, Rachel L Schiesser, Alida J Evans, Kelly J Peyton, William Durante, Jennifer L West, Andrew I Schafer
• Journal: Biochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 291 Issue 4 Pg. 1014-21 (Mar 08 2002) ISSN: 0006-291X [Print] United States
• PMID: 11866467 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Hydrogels
• Indazoles
• Platelet Aggregation Inhibitors
• 3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole
• Polyethylene Glycols
• Cyclic GMP

Topics

• Angioplasty, Balloon (adverse effects)
• Animals
• Arterial Occlusive Diseases (drug therapy, etiology, pathology)
• Blood Platelets (drug effects, physiology)
• Carotid Stenosis (drug therapy, etiology, pathology)
• Cell Adhesion (drug effects)
• Cell Division (drug effects)
• Cells, Cultured
• Cyclic GMP (metabolism)
• Dose-Response Relationship, Drug
• Hydrogels (administration & dosage)
• Indazoles (administration & dosage, pharmacology)
• Muscle, Smooth, Vascular (drug effects, metabolism)
• Platelet Aggregation Inhibitors (administration & dosage, pharmacology)
• Polyethylene Glycols (administration & dosage)
• Rats
• Rats, Sprague-Dawley