Biliverdin administration prevents the formation of intimal hyperplasia induced by vascular injury

Atsunori Nakao, Noriko Murase, Chien Ho, Hideyoshi Toyokawa, Timothy R. Billiar, Shinichi Kanno

Research output: Contribution to journalArticlepeer-review

69 Citations (Scopus)

Abstract

Background - Autologous vein grafts and balloon angioplasty are still commonly used for arterial reconstructive procedures. Their success is limited by the development of intimal hyperplasia (IH). Biliverdin (BVD), one of the by-products of heme degradation, has been shown to have potent antioxidant and antiinflammatory effects. We hypothesized that BVD administration would protect vascular tissue against vascular injury. Methods and Results - The effects of BVD administration against IH after vascular injury were analyzed in an arterialized vein graft model and a balloon injury model in rats. BVD treatment significantly suppressed the development of IH in both models compared with those without BVD. The mechanisms by which BVD treatment inhibits IH development might include decreasing c-Jun NH2 terminal kinase activation and preventing apoptosis of endothelial cells. BVD also suppressed vascular smooth muscle cell migration in vitro. Conclusions - BVD administration prevented IH associated with arterialized vein graft vasculopathy or balloon angioplasty-induced vessel injury. These results suggest that a treatment regimen with exogenous BVD administration could provide an effective therapeutic adjunct to facilitate transfer of experimental treatments for vascular injury to the clinic.

Original languageEnglish
Pages (from-to)587-591
Number of pages5
JournalCirculation
Volume112
Issue number4
DOIs
Publication statusPublished - Jul 26 2005
Externally publishedYes

Keywords

  • Angioplasty
  • Antioxidants
  • Apoptosis
  • Reperfusion
  • Restenosis

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Fingerprint Dive into the research topics of 'Biliverdin administration prevents the formation of intimal hyperplasia induced by vascular injury'. Together they form a unique fingerprint.

Cite this