Effects of Olibanum Extracts on Vascular Cell Adhesion Molecules Expression

유향 추출물이 혈관내피세포 부착단백질 발현에 미치는 영향

  • Lee, Soong-In (Department of Physiology, College of Oriental Medicine, Wonkwang University) ;
  • Kwon, Kang-Beom (Department of Physiology, College of Oriental Medicine, Wonkwang University) ;
  • Han, Jong-Hyun (Department of Pharmacology, College of Oriental Medicine, Wonkwang University) ;
  • Ryu, Do-Gon (Department of Physiology, College of Oriental Medicine, Wonkwang University)
  • 이숭인 (원광대학교 한의과대학 한방생리학교실) ;
  • 권강범 (원광대학교 한의과대학 한방생리학교실) ;
  • 한종현 (원광대학교 한의과대학 약리학교실) ;
  • 류도곤 (원광대학교 한의과대학 한방생리학교실)
  • Received : 2011.03.04
  • Accepted : 2011.05.30
  • Published : 2011.06.25

Abstract

In order to validate the use of Olibanum as an anti-inflammatory drug in the traditional Korean medicine, I have investigated the effect of water-soluble extract of Olibanum (EO) on the expression of pro-inflammatory vascular cell adhesion molecule-1 (VCAM-1) in human umbilical vein endothelial cells (HUVECs) stimulated with tumor necrosis factor-${\alpha}$. The extract inhibited dose-dependently VCAM-1 expression without its cytotoxic effect on HUVECs, as measured by a flow cytometer using fluorescence-enhanced anti-VCAM-1 antibody, and significantly decreased mRNA levels of VCAM-1, as determined using reverse transcription polymerase chain reaction. These results suggest that Olibanum may have therapeutic potential in the control of endothelial disorders caused by inflammation.

Keywords

References

  1. 신민교. 임상본초학. 서울, 남산당, pp 739-740, 1997.
  2. Pungle, P., Banavalikar, M., Suthar, A., Biyani, M., Mengi, S. Immunomodulatory activity of boswellic acids of Boswellia serrata Roxb. Indian J Exp Biol 41(12):1460-1462, 2003.
  3. Badria, F.A., Mikhaeil, B.R., Maatooq, G.T., Amer, M.M. Immunomodulatory triterpenoids from the oleogum resin of Boswellia carterii Birdwood. Z Naturforsch 58(7-8):505-516, 2003.
  4. Hostanska, K., Daum, G., Saller, R. Cytostatic and apoptosis-inducing activity of boswellic acids toward malignant cell lines in vitro. Anticancer Res 22(5):2853-2862, 2002.
  5. Liu, J.J., Nilsson, A., Oredsson, S., Badmaev, V., Zhao, W.Z., Duan, R.D. Boswellic acids trigger apoptosis via a pathway dependent on caspase-8 activation but independent on Fas/Fas ligand interaction in colon cancer HT-29 cells. Carcinogenesis 23(12):2087-2093, 2002. https://doi.org/10.1093/carcin/23.12.2087
  6. Sharma, S., Thawani, V., Hingorani, L., Shrivastava, M., Bhate, V.R., Khiyani, R. Pharmacokinetic study of 11-Keto beta-Boswellic acid. Phytomedicine 11(2-3):255-260, 2004. https://doi.org/10.1078/0944-7113-00290
  7. Lakshmi Niranjan Reddy V., Ravinder, K., Srinivasulu, M., venkateshwar Goud, T., Malla Reddy, S., Srujankumar, D., Prabhakar Rao, T., Suryanarayana Murty, U., Venkateswarlu, Y. Two new macrocyclic diaryl ether heptanoids from Boswellia ovalifoliolata. Chem Pharm Bull 51(9):1081-1084, 2003. https://doi.org/10.1248/cpb.51.1081
  8. Kimmatkar, N., Thawani, V., Hingorani, L., Khiyani, R. Efficacy and tolerability of Boswellia serrata extract in treatment of osteoarthritis of knee a randomized double blind placebo controlled trial. Phytomedicine 10(1):3-7, 2003. https://doi.org/10.1078/094471103321648593
  9. Culioli, G., Mathe, C., Archier, P., Vieillescazes, C. A lupane triterpene from frankincense (Boswellia sp., Burseraceae). Phytochemistry 62(4):537-541, 2003. https://doi.org/10.1016/S0031-9422(02)00538-1
  10. Park, Y.S., Lee, J.H., Bondar, J., Harwalkar, J.A., Safayhi, H., Golubic, M. Cytotoxic action of acetyl-11-keto-beta-boswellic acid (AKBA) on meningioma cells. Planta Med 68(5):397-401, 2002. https://doi.org/10.1055/s-2002-32090
  11. Uriarte, S.M., Molestina, R.E., Miller, R.D., Bernabo, J., Farinati, A., Eiguchi, K., Ramirez, J.A., Summersgill, J.T. Effects of fluoroquinolones on the migration of human phagocytes through Chlamydia pneumoniae-infected and tumor necrosis factor alpha-stimulated endothelial cells. Antimicrob Agents Chemother 48(7):2538-2543, 2004. https://doi.org/10.1128/AAC.48.7.2538-2543.2004
  12. Yang, Y.Y., Hu, C.J., Chang, S.M., Tai, T.Y., Leu, S.J. Aspirin inhibits monocyte chemoattractant protein-1 and interleukin-8 expression in TNF-alpha stimulated human umbilical vein endothelial cells. Atherosclerosis 174(2):207-213, 2004. https://doi.org/10.1016/j.atherosclerosis.2004.01.024
  13. Li, W.G., Gavrila, D., Liu, X., Wang, L., Gunnlaugsson, S., Stoll, L.L., McCormick, M.L., Sigmund, C.D., Tang, C., Weintraub, N.L. Ghrelin inhibits proinflammatory responses and nuclear factor-kappaB activation in human endothelial cells. Circulation 11;109(18):2221-2226, 2004. https://doi.org/10.1161/01.CIR.0000127956.43874.F2
  14. Wagner, A.H., Guldenzoph, B., Lienenluke, B., Hecker, M. CD154/CD40-mediated expression of CD154 in endothelial cells: consequences for endothelial cell-monocyte interaction. Arterioscler Thromb Vasc Biol 24(4):715-720, 2004. https://doi.org/10.1161/01.ATV.0000122853.99978.b1
  15. Murugesan, G., Sandhya Rani M.R., Gerber, C.E., Mukhopadhyay, C., Ransohoff, R.M., Chisolm, G.M., Kottke-Marchant K. Lysophosphatidylcholine regulates human microvascular endothelial cell expression of chemokines. J Mol Cell Cardiol 35(11):1375-1384, 2003. https://doi.org/10.1016/j.yjmcc.2003.08.004
  16. Walton, K.A., Cole, A.L., Yeh, M., Subbanagounder, G., Krutzik, S.R., Modlin, R.L., Lucas, R.M., Nakai, J., Smart, E.J., Vora, D.K., Berliner, J.A. Specific phospholipid oxidation products inhibit ligand activation of toll-like receptors 4 and 2. Arterioscler Thromb Vasc Biol 23(7):1197-1203, 2003. https://doi.org/10.1161/01.ATV.0000079340.80744.B8
  17. Poddar, R., Sivasubramanian, N., DiBello, P.M., Robinson, K., Jacobsen, D.W. Homocysteine induces expression and secretion of monocyte chemoattractant protein-1 and interleukin-8 in human aortic endothelial cells: implications for vascular disease. Circulation 103(22):2717-2723, 2001. https://doi.org/10.1161/01.CIR.103.22.2717
  18. Li, Y., Chi, L., Stechschulte, D.J., Dileepan, K.N. Histamine-induced production of interleukin-6 and interleukin-8 by human coronary artery endothelial cells is enhanced by endotoxin and tumor necrosis factor-alpha. Microvasc Res 61(3):253-262, 2001. https://doi.org/10.1006/mvre.2001.2304
  19. Volin, M.V., Harlow, L.A., Woods, J.M., Campbell, P.L., Amin, M.A., Tokuhira, M., Koch, A.E. Treatment with sulfasalazine or sulfapyridine, but not 5-aminosalicyclic acid, inhibits basic fibroblast growth factor-induced endothelial cell chemotaxis. Arthritis Rheum 42(9):1927-1935, 1999. https://doi.org/10.1002/1529-0131(199909)42:9<1927::AID-ANR19>3.0.CO;2-X
  20. Kayal, S., Lilienbaum, A., Poyart, C., Memet, S., Israel, A., Berche, P. Listeriolysin O-dependent activation of endothelial cells during infection with Listeria monocytogenes: activation of NF-kappa B and upregulation of adhesion molecules and chemokines. Mol Microbiol 31(6):1709-1722, 1999. https://doi.org/10.1046/j.1365-2958.1999.01305.x
  21. Lakshminarayanan, V., Beno, D.W., Costa, R.H., Roebuck, K.A. Differential regulation of interleukin-8 and intercellular adhesion molecule-1 by H2O2 and tumor necrosis factor-alpha in endothelial and epithelial cells. J Biol Chem 272(52):32910-32918, 1997. https://doi.org/10.1074/jbc.272.52.32910
  22. Goebeler, M., Yoshimura, T., Toksoy, A., Ritter, U., Brocker, E.B., Gillitzer, R. The chemokine repertoire of human dermal microvascular endothelial cells and its regulation by inflammatory cytokines. J Invest Dermatol 108(4):445-451, 1997. https://doi.org/10.1111/1523-1747.ep12289711
  23. Lukacs, N.W., Strieter, R.M., Elner, V., Evanoff, H.L., Burdick, M.D., Kunkel, S.L. Production of chemokines, interleukin-8 and monocyte chemoattractant protein-1, during monocyte: endothelial cell interactions. Blood 86(7): 2767-2773, 1995.
  24. Brown, Z., Gerritsen, M.E., Carley, W.W., Strieter, R.M., Kunkel, S.L., Westwick, J. Chemokine gene expression and secretion by cytokine-activated human microvascular endothelial cells. Differential regulation of monocyte chemoattractant protein-1 and interleukin-8 in response to interferon-gamma. Am J Pathol 145(4):913-921, 1994.
  25. Zhao, B., Stavchansky, S.A., Bowden, R.A., Bowman, P.D. Effect of interleukin-1beta and tumor necrosis factor-alpha on gene expression in human endothelial cells. Am J Physiol Cell Physiol 284(6):C1577-1583, 2003. https://doi.org/10.1152/ajpcell.00243.2002
  26. Fiuza, C., Bustin, M., Talwar, S., Tropea, M., Gerstenberger, E,. Shelhamer, J.H., Suffredini, A.F. Inflammation-promoting activity of HMGB1 on human microvascular endothelial cells. Blood 101(7):2652-2660, 2002.
  27. Unger, R.E., Krump-Konvalinkova V., Peters, K., Kirkpatrick, C.J. In vitro expression of the endothelial phenotype: comparative study of primary isolated cells and cell lines, including the novel cell line HPMEC-ST1.6R. Microvasc Res 64(3):384-397, 2002. https://doi.org/10.1006/mvre.2002.2434