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Evidence-Based Complementary and Alternative Medicine
Volume 2016, Article ID 3284704, 7 pages
http://dx.doi.org/10.1155/2016/3284704
Research Article

Rhus javanica Gall Extract Inhibits the Differentiation of Bone Marrow-Derived Osteoclasts and Ovariectomy-Induced Bone Loss

1Biomedical Research Institute, Kyungpook National University Hospital, Daegu 41940, Republic of Korea
2Skeletal Diseases Genome Research Center, Kyungpook National University Hospital, Daegu 41940, Republic of Korea
3Department of Oral Pathology and Regenerative Medicine, School of Dentistry, IHBR, Kyungpook National University, Daegu 41940, Republic of Korea
4Department of Ophthalmology, Graduate School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea
5Department of Orthopedic Surgery, Graduate School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea
6School of Food Science & Biotechnology, Kyungpook National University, Daegu 41566, Republic of Korea

Received 29 February 2016; Revised 27 April 2016; Accepted 10 May 2016

Academic Editor: Yoshiki Mukudai

Copyright © 2016 Tae-Ho Kim et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. L. M. McNamara, “Perspective on post-menopausal osteoporosis: establishing an interdisciplinary understanding of the sequence of events from the molecular level to whole bone fractures,” Journal of the Royal Society Interface, vol. 7, no. 44, pp. 353–372, 2010. View at Publisher · View at Google Scholar · View at Scopus
  2. W. J. Boyle, W. S. Simonet, and D. L. Lacey, “Osteoclast differentiation and activation,” Nature, vol. 423, no. 6937, pp. 337–342, 2003. View at Publisher · View at Google Scholar · View at Scopus
  3. D. Goltzman, “Discoveries, drugs and skeletal disorders,” Nature Reviews Drug Discovery, vol. 1, no. 10, pp. 784–796, 2002. View at Publisher · View at Google Scholar · View at Scopus
  4. P. J. Kelly, “Is osteoporosis a genetically determined disease?” British Journal of Obstetics and Gynaecology, vol. 103, supplement 13, pp. 20–27, 1996. View at Google Scholar
  5. B. L. Riggs, S. Khosla, and L. J. Melton III, “Sex steroids and the construction and conservation of the adult skeleton,” Endocrine Reviews, vol. 23, no. 3, pp. 279–302, 2002. View at Publisher · View at Google Scholar · View at Scopus
  6. R. Pacifi, “Editorial: cytokines, estrogen, and postmenopausal osteoporosis—the second decade,” Endocrinology, vol. 139, no. 6, pp. 2659–2661, 1998. View at Publisher · View at Google Scholar · View at Scopus
  7. M. N. Weitzmann and R. Pacifici, “Estrogen deficiency and bone loss: an inflammatory tale,” Journal of Clinical Investigation, vol. 116, no. 5, pp. 1186–1194, 2006. View at Publisher · View at Google Scholar · View at Scopus
  8. G. A. Rodan and T. J. Martin, “Therapeutic approaches to bone diseases,” Science, vol. 289, no. 5484, pp. 1508–1514, 2000. View at Publisher · View at Google Scholar · View at Scopus
  9. I. R. Reid, “Pharmacotherapy of osteoporosis in postmenopausal women: focus on safety,” Expert Opinion on Drug Safety, vol. 1, no. 1, pp. 93–107, 2002. View at Publisher · View at Google Scholar · View at Scopus
  10. I.-T. Yeh, “Postmenopausal hormone replacement therapy: endometrial and breast effects,” Advances in Anatomic Pathology, vol. 14, no. 1, pp. 17–24, 2007. View at Publisher · View at Google Scholar · View at Scopus
  11. M. Jia, Y. Nie, D.-P. Cao et al., “Potential antiosteoporotic agents from plants: a comprehensive review,” Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 364604, 28 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus
  12. S. H. Lee and S. H. Lee, “Comparison of antioxidant activity and α-glucosidase inhibiting activity by extracts of Rhus javanica,” Current Research on Agriculture and Life Sciences, vol. 31, no. 4, pp. 227–232, 2013. View at Publisher · View at Google Scholar
  13. J. G. Choi, S. H. Mun, H. S. Chahar et al., “Methyl gallate from Rhus javanica successfully controls clinical isolates of Salmonella infection in both in vitro and in vivo systems,” PLoS ONE, vol. 9, no. 7, Article ID e102697, 7 pages, 2014. View at Google Scholar
  14. R.-B. An, H. Oh, and Y.-C. Kim, “Phenolic constituents of Galla Rhois with hepatoprotective effects on tacrine- and nitrofurantoin-induced cytotoxicity in Hep G2 cells,” Biological and Pharmaceutical Bulletin, vol. 28, no. 11, pp. 2155–2157, 2005. View at Publisher · View at Google Scholar · View at Scopus
  15. O. J. Kwon, J.-S. Bae, H. Y. Lee et al., “Pancreatic lipase inhibitory gallotannins from galla rhois with inhibitory effects on adipocyte differentiation in 3T3-L1 cells,” Molecules, vol. 18, no. 9, pp. 10629–10638, 2013. View at Publisher · View at Google Scholar · View at Scopus
  16. T. Okuda, T. Yoshida, and T. Hatano, “Hydrolyzable tannins and related polyphenols,” Fortschritte der Chemie Oganischer Naturstoffe, vol. 66, no. 1, pp. 1–117, 1995. View at Google Scholar
  17. A. M. Sciuto and T. S. Moran, “Effect of dietary treatment with n-propyl gallate or vitamin E on the survival of mice exposed to phosgene,” Journal of Applied Toxicology, vol. 21, no. 1, pp. 33–39, 2001. View at Publisher · View at Google Scholar · View at Scopus
  18. T.-J. Hsieh, T.-Z. Liu, Y.-C. Chia et al., “Protective effect of methyl gallate from Toona sinensis (Meliaceae) against hydrogen peroxide-induced oxidative stress and DNA damage in MDCK cells,” Food and Chemical Toxicology, vol. 42, no. 5, pp. 843–850, 2004. View at Publisher · View at Google Scholar · View at Scopus
  19. C. Granéli, A. Thorfve, U. Ruetschi et al., “Novel markers of osteogenic and adipogenic differentiation of human bone marrow stromal cells identified using a quantitative proteomics approach,” Stem Cell Research, vol. 12, no. 1, pp. 153–165, 2014. View at Publisher · View at Google Scholar · View at Scopus
  20. G. H. Byung, J. M. Hong, J.-Y. Park et al., “Proteomic profile of osteoclast membrane proteins: identification of Na+/H+ exchanger domain containing 2 and its role in osteoclast fusion,” Proteomics, vol. 8, no. 13, pp. 2625–2639, 2008. View at Publisher · View at Google Scholar · View at Scopus
  21. Y. W. O. Kim, S.-H. Baek, S.-H. Lee, T.-H. Kim, and S.-Y. Kim, “Fucoidan, a sulfated polysaccharide, inhibits osteoclast differentiation and function by modulating RANKL signaling,” International Journal of Molecular Sciences, vol. 15, no. 10, pp. 18840–18855, 2014. View at Publisher · View at Google Scholar · View at Scopus
  22. D. N. Kalu, “The ovariectomized rat model of postmenopausal bone loss,” Bone and Mineral, vol. 15, no. 3, pp. 175–191, 1991. View at Publisher · View at Google Scholar · View at Scopus
  23. J. H. Kinney, D. L. Haupt, M. Balooch, A. J. C. Ladd, J. T. Ryaby, and N. E. Lane, “Three-dimensional morphometry of the L6 vertebra in the ovariectomized rat model of osteoporosis: biomechanical implications,” Journal of Bone and Mineral Research, vol. 15, no. 10, pp. 1981–1991, 2000. View at Publisher · View at Google Scholar · View at Scopus
  24. M. Notoya, R. Arai, T. Katafuchi, N. Minamino, and H. Hagiwara, “A novel member of the calcitonin gene-related peptide family, calcitonin receptor-stimulating peptide, inhibits the formation and activity of osteoclasts,” European Journal of Pharmacology, vol. 560, no. 2-3, pp. 234–239, 2007. View at Publisher · View at Google Scholar · View at Scopus
  25. H.-S. Chae, O.-H. Kang, J.-G. Choi et al., “Methyl gallate inhibits the production of interleukin-6 and nitric oxide via down-regulation of extracellular-signal regulated protein kinase in RAW 264.7 cells,” American Journal of Chinese Medicine, vol. 38, no. 5, pp. 973–983, 2010. View at Publisher · View at Google Scholar · View at Scopus
  26. P.-H. Park, J. Hur, Y.-C. Kim, R.-B. An, and D. H. Sohn, “Involvement of heme oxygenase-1 induction in inhibitory effect of ethyl gallate isolated from Galla Rhois on nitric oxide production in RAW 264.7 macrophages,” Archives of Pharmacal Research, vol. 34, no. 9, pp. 1545–1552, 2011. View at Publisher · View at Google Scholar · View at Scopus
  27. K. Lee, J. Kim, B. J. Lee et al., “Protective effects of Rhus javanica, the excrescence produced by the sumac aphid, Schlechtendalia chinensis, on transient focal cerebral ischemia in the rat,” Journal of Insect Science, vol. 12, no. 1, article 10, 12 pages, 2012. View at Google Scholar