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Inhibition of VLA-4/VCAM-1-mediated Cell Adhesion by Triterpenoid Saponins from Bupleurum falcatum L

  • Lee, Seung-Woong (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Kim, Min-Seok (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Lim, Ju-Hwan (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Chang, Jong-Sun (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Ling, Jin (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Bae, Ki-Hwan (College of Pharmacy, Chungnam National University) ;
  • Lee, Woo-Song (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Rho, Mun-Chual (Eco-friendly Biomaterial Research Center, Korea Research Institute of Bioscience and Biotechnology)
  • Received : 2010.01.27
  • Accepted : 2010.05.03
  • Published : 2010.07.20

Abstract

Discovery and isolation of compounds capable of blocking the interactions between VCAM-1 and VLA-4, a major pair of adhesion molecules contributing to the different steps of leukocyte migration across the endothelium in inflammatory responses, has been a major goal of this lab. Through bioactivity-guided fractionation, five saikosaponins were subsequently isolated from the methanol extracts of the roots of Bupleurum falcatum L. Their structures were elucidated by spectroscopic analysis ($^1H-$, $^{13}C$-NMR and 2D-NMR), as follows, saikosaponins: A (1); D (2); C (3); B3 (4); B4 (5). Compounds 1 and 2 inhibited interaction of sVCAM-1 and VLA-4 of THP-1 cells with respective $IC_{50}$ values of 7.8 and 1.7 ${\mu}M$. The aglycone structure of 2 also showed cell adhesion inhibitory activity with an $IC_{50}$ value of 21.1 ${\mu}M$. With these results, we suspect these two saikosaponins from the Bupleurum falcatum L. roots to be prime candidates for therapeutic strategies towards inflammation.

Keywords

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