Inhibition of cell surface expression of endothelial adhesion molecules by ursolic acid prevents intimal hyperplasia of venous bypass grafts in rats

Eur J Cardiothorac Surg. 2012 Nov;42(5):878-84. doi: 10.1093/ejcts/ezs128. Epub 2012 May 2.

Abstract

Objectives: Despite rapid progress in surgical techniques, there is still a significant lack of surgery-supportive pharmacological treatments. The aim of this study was to test the hypothesis that ursolic acid (UA) may prevent intimal hyperplasia of venous bypass grafts.

Methods: The hypothesis was tested by means of primary cell isolation and culture followed by real-time polymerase chain reaction, western blotting, fluorescence microscopy and fluorescence-activated cell sorting analyses, as well as an in vivo rat model for intimal hyperplasia of venous bypass grafts and immunohistochemistry and histochemistry.

Results: The local application of UA significantly inhibited intimal hyperplasia in vivo (intimal thickness control: 25 µm, UA group: 18 µM-8 weeks after surgery). The UA treatment of grafts significantly resulted in reduced endothelial vascular cell adhesion molecule-1 (VCAM-1) expression, reduced infiltration of the grafts vessel wall by CD45-positive cells and increased smooth muscle cell (SMC) death. In in vitro condition, it could be shown that UA inhibits VCAM-1 expression downstream of NFκB and is likely to interfere with VCAM-1 protein synthesis in endothelial cells. Quantification of cell death in vascular smooth muscle cells treated with UA indicated that UA is a potent inducer of SMC apoptosis.

Conclusions: Our results suggest that UA-mediated inhibition of endothelial VCAM-1 expression reduces the infiltration of venous bypass grafts by CD45-positive cells and inhibits intimal hyperplasia. Apoptosis induction in SMCs may be another method in which UA reduces intimal thickening. UA may constitute a surgery-supportive pharmacon that reduces intimal hyperplasia of vein grafts.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Biomarkers / metabolism
  • Blotting, Western
  • Cardiovascular Agents / pharmacology
  • Cardiovascular Agents / therapeutic use*
  • Cell Survival / drug effects
  • Flow Cytometry
  • Graft Occlusion, Vascular / metabolism
  • Graft Occlusion, Vascular / pathology
  • Graft Occlusion, Vascular / prevention & control*
  • Hyperplasia / metabolism
  • Hyperplasia / pathology
  • Hyperplasia / prevention & control
  • Jugular Veins / metabolism
  • Jugular Veins / pathology
  • Jugular Veins / transplantation*
  • Leukocyte Common Antigens / metabolism
  • Male
  • Microscopy, Fluorescence
  • Rats
  • Rats, Wistar
  • Real-Time Polymerase Chain Reaction
  • Treatment Outcome
  • Triterpenes / pharmacology
  • Triterpenes / therapeutic use*
  • Tunica Intima / drug effects
  • Tunica Intima / pathology*
  • Ursolic Acid
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Vascular Grafting*

Substances

  • Biomarkers
  • Cardiovascular Agents
  • Triterpenes
  • Vascular Cell Adhesion Molecule-1
  • Leukocyte Common Antigens
  • Ptprc protein, rat