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Effect of Hijikia fusiforme extracts on degenerative osteoarthritis in vitro and in vivo models

  • Kwon, Han Ol (Department of Medical Nutrition, Kyung Hee University) ;
  • Lee, Minhee (Department of Medical Nutrition, Kyung Hee University) ;
  • Kim, Ok-Kyung (Department of Medical Nutrition, Kyung Hee University) ;
  • Ha, Yejin (Department of Medical Nutrition, Kyung Hee University) ;
  • Jun, Woojin (Division of Food and Nutritional Science, Chonnam National University) ;
  • Lee, Jeongmin (Department of Medical Nutrition, Kyung Hee University)
  • Received : 2015.08.26
  • Accepted : 2016.01.06
  • Published : 2016.06.01

Abstract

BACKGROUND/OBJECTIVES: The inhibitory effect of Hijikia fusiforme (HF) extracts on degenerative osteoarthritis was examined in primary cultured rat cartilage cells and a monosodium iodoacetate (MIA)-induced osteoarthritis rat model. MATERIALS/METHODS: In vitro, cell survival and the expression of matrix metalloproteinases (MMPs), collagen type I, collagen type II, aggrecan, and tissue inhibitor of metalloproteinases (TIMPs) was measured after $H_2O_2$ ($800{\mu}M$, 2 hr) treatment in primary chondrocytes. In vivo animal study, osteoarthritis was induced by intra-articular injection of MIA into knee joints of rats, and then RH500, HFE250 and HFE500 were administered orally once a day for 28 days. To determine the anti-inflammatory effects of HFE, nitric oxide (NO), prostaglandin $E_2$ ($PGE_2$) expression were measured. In addition, real-time PCR was performed to measure the genetic expression of MMPs, collagen type I, collagen type II, aggrecan, and TIMPs. RESULTS: In the in vitro assay, cell survival after $H_2O_2$ treatment was increased by HFE extract (20% EtOH). In addition, anabolic factors (genetic expression of collagen type I, II, and aggrecan) were increased by HFE extract (20% EtOH). However, the genetic expression of MMP-3 and 7, known as catabolic factors were significantly inhibited by treatment with HFE extract (20% EtOH). In the in vivo assay, anabolic factors (genetic expression of collagen type I, II, aggrecan, and TIMPs) were increased by oral administration of HFE extract. However, the genetic expression of MMP-3 and 7, known as catabolic factors, and production of NO and $PGE_2$ were significantly inhibited by treatment with oral administration of HFE extract. CONCLUSION: HFE extract inhibited articular cartilage degeneration through preventing extracellular matrix degradation and chondrocyte injury.

Keywords

References

  1. Ministry of Health and Welfare, Korea Centers for Disease Control and Prevention. Korea Health Statistics 2012: Korea National Health and Nutrition Examination Survey (KNHANES V-3). Cheongwon: Korea Centers for Disease Control and Prevention: 2013.
  2. Statistics Korea. Senior Statistical Reports. Daejeon: Statistics Korea: 2010.
  3. Garner BC, Stoker AM, Kuroki K, Evans R, Cook CR, Cook JL. Using animal models in osteoarthritis biomarker research. J Knee Surg 2011;24:251-64. https://doi.org/10.1055/s-0031-1297361
  4. Nam DE, Kim OK, Shim TJ, Kim JH, Lee J. Effect of Boswellia serrata extracts on degenerative osteoarthritis in vitro and in vivo models. J Korean Soc Food Sci Nutr 2014;43:631-40. https://doi.org/10.3746/jkfn.2014.43.5.631
  5. Lee JH, Fitzgerald JB, Dimicco MA, Grodzinsky AJ. Mechanical injury of cartilage explants causes specific time-dependent changes in chondrocyte gene expression. Arthritis Rheum 2005;52:2386-95. https://doi.org/10.1002/art.21215
  6. Roy S, Khanna S, Krishnaraju AV, Subbaraju GV, Yasmin T, Bagchi D, Sen CK. Regulation of vascular responses to inflammation: inducible matrix metalloproteinase-3 expression in human microvascular endothelial cells is sensitive to antiinflammatory Boswellia. Antioxid Redox Signal 2006;8:653-60. https://doi.org/10.1089/ars.2006.8.653
  7. Lee V, Cao L, Zhang Y, Kiani C, Adams ME, Yang BB. The roles of matrix molecules in mediating chondrocyte aggregation, attachment, and spreading. J Cell Biochem 2000;79:322-33. https://doi.org/10.1002/1097-4644(20001101)79:2<322::AID-JCB150>3.0.CO;2-U
  8. Korea Health Industry Development Institute. Health Functional Food Industry Development Assistance Report 2011. Cheongwon: Korea Health Industry Development Institute 2011.
  9. Jeon MH, Kim M. Effect of Hijikia fusiforme Fractions on Proliferation and Differentiation in Osteoblastic MC3T3-E1 Cells. J Life Sci 2011;21:300-8. https://doi.org/10.5352/JLS.2011.21.2.300
  10. Kim JA, Lee JM. The change of biologically functional compounds and antioxidant activities in Hizikia fusiformis with drying methods. Korean J Food Cult 2004;19:200-8.
  11. Kapoor M, Martel-Pelletier J, Lajeunesse D, Pelletier JP, Fahmi H. Role of proinflammatory cytokines in the pathophysiology of osteoarthritis. Nat Rev Rheumatol 2011;7:33-42. https://doi.org/10.1038/nrrheum.2010.196
  12. Ministry for Food, Agriculture, Forestry and Fisheries; Korea Food Research Institute. Development of Instant Health Foods Using Hijiki. Gwacheon: Ministry for Food, Agriculture, Forestry and Fisheries; 1997.
  13. Watanabe T, Hirayama T, Takahashi T, Kokubo T, Ikeda M. Toxicological evaluation of arsenic in edible seaweed, Hizikia species. Toxicology 1979;14:1-22. https://doi.org/10.1016/0300-483X(79)90088-X
  14. Dobashi K, Nishino T, Fujihara M, Nagumo T. Isolation and preliminary characterization of fucose-containing sulfated polysaccharides with blood-anticoagulant activity from the brown seaweed Hizikia fusiforme. Carbohydr Res 1989;194:315-20. https://doi.org/10.1016/0008-6215(89)85032-3
  15. Holan ZR, Volesky B. Biosorption of lead and nickel by biomass of marine algae. Biotechnol Bioeng 1994;43:1001-9. https://doi.org/10.1002/bit.260431102
  16. Jeong SC, Jeong YT, Lee SM, Kim JH. Immune-modulating activities of polysaccharides extracted from brown algae Hizikia fusiforme. Biosci Biotechnol Biochem 2015;79:1362-5. https://doi.org/10.1080/09168451.2015.1018121
  17. Mathy-Hartert M, Martin G, Devel P, Deby-Dupont G, Pujol JP, Reginster JY, Henrotin Y. Reactive oxygen species downregulate the expression of pro-inflammatory genes by human chondrocytes. Inflamm Res 2003;52:111-8. https://doi.org/10.1007/s000110300023
  18. Asada S, Fukuda K, Oh M, Hamanishi C, Tanaka S. Effect of hydrogen peroxide on the metabolism of articular chondrocytes. Inflamm Res 1999;48:399-403. https://doi.org/10.1007/s000110050478
  19. Khan IM, Gilbert SJ, Caterson B, Sandell LJ, Archer CW. Oxidative stress induces expression of osteoarthritis markers procollagen IIA and 3B3(-) in adult bovine articular cartilage. Osteoarthritis Cartilage 2008;16:698-707. https://doi.org/10.1016/j.joca.2007.10.004
  20. Catrina AI, Lampa J, Ernestam S, af Klint E, Bratt J, Klareskog L, Ulfgren AK. Anti-tumour necrosis factor (TNF)-alpha therapy (etanercept) down-regulates serum matrix metalloproteinase (MMP)-3 and MMP-1 in rheumatoid arthritis. Rheumatology (Oxford) 2002;41:484-9. https://doi.org/10.1093/rheumatology/41.5.484
  21. Houssiau FA, Devogelaer JP, Van Damme J, de Deuxchaisnes CN, Van Snick J. Interleukin-6 in synovial fluid and serum of patients with rheumatoid arthritis and other inflammatory arthritides. Arthritis Rheum 1988;31:784-8. https://doi.org/10.1002/art.1780310614
  22. Tchetverikov I, Lohmander LS, Verzijl N, Huizinga TW, TeKoppele JM, Hanemaaijer R, DeGroot J. MMP protein and activity levels in synovial fluid from patients with joint injury, inflammatory arthritis, and osteoarthritis. Ann Rheum Dis 2005;64:694-8. https://doi.org/10.1136/ard.2004.022434
  23. Wink DA, Hines HB, Cheng RY, Switzer CH, Flores-Santana W, Vitek MP, Ridnour LA, Colton CA. Nitric oxide and redox mechanisms in the immune response. J Leukoc Biol 2011;89:873-91. https://doi.org/10.1189/jlb.1010550
  24. Thomas CM, Fuller CJ, Whittles CE, Sharif M. Chondrocyte death by apoptosis is associated with the initiation and severity of articular cartilage degradation. Int J Rheum Dis 2011;14:191-8. https://doi.org/10.1111/j.1756-185X.2010.01578.x
  25. Vane JR, Bakhle YS, Botting RM. Cyclooxygenases 1 and 2. Annu Rev Pharmacol Toxicol 1998;38:97-120. https://doi.org/10.1146/annurev.pharmtox.38.1.97
  26. Bensen WG, Fiechtner JJ, McMillen JI, Zhao WW, Yu SS, Woods EM, Hubbard RC, Isakson PC, Verburg KM, Geis GS. Treatment of osteoarthritis with celecoxib, a cyclooxygenase-2 inhibitor: a randomized controlled trial. Mayo Clin Proc 1999;74:1095-105. https://doi.org/10.4065/74.11.1095
  27. Hardy MM, Seibert K, Manning PT, Currie MG, Woerner BM, Edwards D, Koki A, Tripp CS. Cyclooxygenase 2-dependent prostaglandin $E_2$ modulates cartilage proteoglycan degradation in human osteoarthritis explants. Arthritis Rheum 2002;46:1789-803. https://doi.org/10.1002/art.10356
  28. Combe R, Bramwell S, Field MJ. The monosodium iodoacetate model of osteoarthritis: a model of chronic nociceptive pain in rats? Neurosci Lett 2004;370:236-40. https://doi.org/10.1016/j.neulet.2004.08.023
  29. Kim MJ, Lee HH, Jeong JW, Seo MJ, Kang BW, Park JU, Kim KS, Cho YS, Seo KI, Kim GY, Kim JI, Choi YH, Jeong YK. Anti-inflammatory effects of 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone via NF- B inactivation in lipopolysaccharide-stimulated RAW 264.7 macrophage. Mol Med Rep 2014;9:1197-203. https://doi.org/10.3892/mmr.2014.1922

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