[The effect of nuclear transcription factor-kappaB decoy oligodeoxynucleotides on the intimal hyperplasia in vein graft]

Zhonghua Wai Ke Za Zhi. 2003 Sep;41(9):684-7.
[Article in Chinese]

Abstract

Objective: To investigate the effect of nuclear transcription factor-kappaB decoy oligodeoxynucleotides (NFkappaB decoyODNs) on the intimal hyperplasia (IH) in vein graft in rats.

Methods: Autogenous vein graft model for 72 Wistar rats was established, and the interior jugular vein was transplanted to common jugular artery by microsurgical technique. The rats were divided into 6 groups according to different processing methods, including NFkappaB decoyODNs 50 microg and 200 microg, scramble decoyODNs 50 microg and 200 microg, control and lipofectin + pluronic teams. Vein graft samples were harvested in 1 or 2 weeks after surgery and ICAM-1 mRNA were measured by RT-PCR. Western blotting and immunohistochemistry methods were also employed to detect the expression of p65 and ICAM-1. IH was compared at the same time.

Results: The intimal hyperplasia was evident in 1 or 2 weeks after vein graft, and ameliorated by 50 microg of NFkappaB decoyODNs with inhibition rate from 22% to 31%, 200 microg of NFkappaB decoyODNs had a higher inhibition rate from 41% to 53%. However, no effect was found in the other teams. The expression of ICAM-1 mRNA was also inhibited significantly by NFkappaB decoyODNs and more obvious in 2 weeks after surgery. Expression of ICAM-1 and p65 decreased greatly in NFkappaB decoyODNs team, which has a inhibition rate from 30% to 57%.

Conclusion: Transfection of NFkappaB decoyODNs can inhibit the IH after vein graft, which may be accomplished by the inhibition of gene expression of ICAM-1.

Publication types

  • English Abstract

MeSH terms

  • Animals
  • Blotting, Western
  • Female
  • Genetic Therapy / methods*
  • Hyperplasia
  • Immunohistochemistry
  • Intercellular Adhesion Molecule-1 / genetics
  • Jugular Veins / pathology
  • Jugular Veins / transplantation*
  • Male
  • NF-kappa B / genetics*
  • Oligodeoxyribonucleotides / pharmacology*
  • RNA, Messenger / analysis
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tunica Intima / pathology*

Substances

  • NF-kappa B
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • Intercellular Adhesion Molecule-1