YC-1, a benzyl indazole derivative, stimulates vascular cGMP and inhibits neointima formation

Biochem Biophys Res Commun. 2000 Dec 20;279(2):646-52. doi: 10.1006/bbrc.2000.3942.

Abstract

The pathobiologic process of arterial stenosis following balloon angioplasty continues to be an enigmatic problem in clinical settings. This research project investigates the ability of YC-1, a benzyl indazole derivative that sensitizes sGC/cGMP, to stimulate endogenous cGMP and attenuate balloon injury-induced neointima (NI) formation in the rat carotid artery. Northern and Western blot analyses revealed enhanced acute expression of iNOS and inducible heme oxygenase (HO-1) mRNA and protein in the injured artery. The contralateral uninjured artery also demonstrated acute HO-1 mRNA and protein induction without detectable iNOS expression. Perivascular application of YC-1 immediately following injury significantly stimulated acute vessel wall cGMP compared to untreated controls. YC-1 treated sections demonstrated significant reduction in NI area (-74%), NI area/medial wall area (-72%), and NI thickness (-76%) 2 weeks post-injury. These results directly implicate YC-1 as a potent new therapeutic agent capable of reducing post-angioplasty stenosis through endogenous CO- and/or NO-mediated, cGMP-dependent processes.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Angioplasty, Balloon / adverse effects*
  • Animals
  • Carotid Arteries / drug effects
  • Carotid Arteries / enzymology
  • Carotid Arteries / physiology*
  • Carotid Artery Injuries / etiology
  • Carotid Artery Injuries / prevention & control
  • Carotid Stenosis / physiopathology
  • Carotid Stenosis / therapy
  • Cyclic GMP / metabolism*
  • Gene Expression Regulation, Enzymologic / drug effects
  • Heme Oxygenase (Decyclizing) / genetics
  • Heme Oxygenase-1
  • Indazoles / pharmacology*
  • Male
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase Type II
  • Platelet Aggregation Inhibitors / pharmacology*
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Recurrence
  • Transcription, Genetic / drug effects
  • Tunica Intima / drug effects
  • Tunica Intima / enzymology
  • Tunica Intima / physiology*

Substances

  • Indazoles
  • Platelet Aggregation Inhibitors
  • RNA, Messenger
  • 3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, rat
  • Heme Oxygenase (Decyclizing)
  • Heme Oxygenase-1
  • Cyclic GMP