Log in

Suppressive effects of Anoectochilus formosanus extract on osteoclast formation in vitro and bone resorption in vivo

  • Original Article
  • Published:
Journal of Bone and Mineral Metabolism Aims and scope Submit manuscript

Abstract

Anoectochilus formosanus, a plant native to Taiwan, is used as a folk medicine. It was found that oral administration of A. formosanus extract (AFE) (500 mg/kg) for 4 weeks suppressed bone weight loss and trabecular bone loss in ovariectomized mice, an experimental model of osteoporosis. Although AFE at 12.5 and 25 μg/ml inhibited osteoclast formation in co-culture of osteoblasts and bone marrow cells, AFE did not inhibit the formation of osteoclast progenitor cells and preosteoclast cells in bone marrow cells and RAW264 cells. However, AFE (at 12.5 and 25 μg/ml) decreased RANKL expression. These results suggested that AFE might suppress the bone loss caused by estrogen deficiency through suppression of RANKL expression required for osteoclast formation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Arnaud CD, Kolb FO (1986) The calcitropic hormones and metabolic bone disease. In: Basic & Clinical Endocrinology. Lange, Los Altos, pp 202–271

    Google Scholar 

  2. Lin CC, Huang PC, Lin JM (2000) Antioxidant and hepatoprotective effects of Anoectochilus formosanus and Gynostema pentaphyllum. Am J Chin Med 28:87–96

    Article  PubMed  CAS  Google Scholar 

  3. Shih CC, Wu YW, Lin WJ (2002) Antihyperblycemic and antioxidant properties of Anoectochilus formosanus in diabetic rats. Clin Exp Pharmacol Physiol 29:684–688

    Article  PubMed  CAS  Google Scholar 

  4. Lin JM, Lin CC, Chiu H (1993) Evaluation of the anti-inflammatory and liver protective effects of Anoectochilus formosanus, Ganoderma lucidum, and Gynostemma pentaphillum in rats. Am J Chin Med 21:59–69

    Article  PubMed  CAS  Google Scholar 

  5. Shih CC, Wu YW, Lin WC (2001) Ameliorative effects of Anoectochilus formosanus extract on osteopenia in ovariectomized rats. J Ethnopharmacol 77:233–238

    Article  PubMed  CAS  Google Scholar 

  6. Yamaguchi K, Hayama T, Makita T, Tsuji T (1997) Time course of bone biomechanical parameters in ovariectomized mice. J Bone Miner Metab 15:138–144

    Article  Google Scholar 

  7. Baron R (1989) Molecular mechanisms of bone resorption by the osteoclast. Anat Rec 224:317–324

    Article  PubMed  CAS  Google Scholar 

  8. Suda T, Takahashi N, Martin TJ (1992) Modulation of osteoclast differentiation. Endocr Rev 13:66–80

    Article  PubMed  CAS  Google Scholar 

  9. Miura M, Tanaka K, Komatsu Y, Suda M, Yasuda A, Sakuma Y, Ozasa A, Nakao K (2002) A novel interaction between thyroid hormones and 1,25(OH)(2)D(3) in osteoclast formation. Biochem Biophys Res Commun 291:987–994

    Article  PubMed  CAS  Google Scholar 

  10. Hsu H, Lacey D, Dunstan CR, Solovyev I, Colombero A, et al (1999) Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand. Proc Natl Acad Sci USA 96:3540–3545

    Article  PubMed  CAS  Google Scholar 

  11. Jimi E, Akiyama S, Tsurukai T, Okahashi N, Kobayashi K, Udagawa N, Nishihara T, Takahashi N, Suda T (1999) Osteoclast differentiation factor acts as a multifunctional regulator in murine osteoclast differentiation and function. J Immunol 163:434–442

    PubMed  CAS  Google Scholar 

  12. Yamaguchi K, Yada M, Tsuji T, Kuramoto M, Uemura D (1999) Suppressive effect of norzoanthamine hydrochloride on experimental osteoporosis in ovariectomized mice. Biol Pharm Bull 22: 920–924

    PubMed  CAS  Google Scholar 

  13. Parfitt AM, Mathews CHE, Villanueva AR, Kleerekoper M (1983) Relationships between surface, volume, and thickness of iliac trabecular bone in aging and osteoporosis. J Clin Invest 72: 1396–1409

    Article  PubMed  CAS  Google Scholar 

  14. Kodama H, Nose M, Niida S, Yamazaki A (1991) Essential role of macrophage colony-stimulating factor in the osteoclast differentiation supported by stromal cells. J Exp Med 173:1291–1294

    Article  PubMed  CAS  Google Scholar 

  15. Kodama H, Yamazaki A, Nose M, Niida S, Ohgame Y, Abe M, Kumegawa M, Suda T (1991) Congenital osteoclast deficiency in osteopetrotic (op/op) mice is cured by injenctions of macrophage colony-stimulating factor. J Exp Med 173:269–272

    Article  PubMed  CAS  Google Scholar 

  16. Takahashi N, Udagawa N, Suda T (1998) A new member of tumor necrosis factor ligand family, ODF/OPGL/TRANCE/RANKL, regulates osteoclast differentiation and function. J Biol Chem 273: 27091–27096

    Article  Google Scholar 

  17. Itonaga I, Sabokbar A, Sun SG, Kudo O, Danks L, Ferguson D, Fujikawa Y, Athanasou NA (2004) Transforming growth factor-β induces osteoclast formation in the absence of RANKL. Bone (NY) 34:57–64

    CAS  Google Scholar 

  18. Quinn JM, Elliott J, Gillespie MT, Martin TJ (1998) A combination of osteoclast differentiation factor and macrophage colony-stimulating factor is sufficient for both human and mouse osteoclast formation in vitro. Endocrinology 139:4424–4427

    Article  PubMed  CAS  Google Scholar 

  19. Gyda M, Corisdeo S, Zaidi M, Troen BR (2001) Macrophage colony-stimulating factor suppress osteoblast formation. Biochem Biophys Res 285:328–334

    Article  CAS  Google Scholar 

  20. Nakagawa N, Kinosaki M, Tamaguchi K, Shima N, Yasuda H, Yano K, Morinaga T, Higashio K (1998) RANK is the essential signaling receptor for osteoclast differentiation factor in osteoclastgenesis. Biochem Biophys Res Commun 253:395–400

    Article  PubMed  CAS  Google Scholar 

  21. Fuller K, Wong B, Fox S, Choi Y, Chambers TJ (1998) TRANCE is necessary and sufficient for osteoblast-medicated activation of bone resorption in osteoclasts. J Exp Med 188:997–1001

    Article  PubMed  CAS  Google Scholar 

  22. Woo JT, Nakagawa H, Kotoya M, Yonezawa T, Udagawa N, Lee IS, Ohnishi M, Hagiwara H, Nagai K (2004) Quercetin suppress bone resorption by inhibiting the differentiation and activation of osteoclasts. Biol Pharm Bull 27:504–509

    Article  PubMed  CAS  Google Scholar 

  23. Uchiyama S, Yamaguchi M (2004) Inhibitory effect of β-cryptoxanthin on osteoclast—like cell formation in mouse marrow cultures. Biochem Pharm 67:1297–1305

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kazunaga Yazawa.

About this article

Cite this article

Masuda, K., Ikeuchi, M., Koyama, T. et al. Suppressive effects of Anoectochilus formosanus extract on osteoclast formation in vitro and bone resorption in vivo. J Bone Miner Metab 26, 123–129 (2008). https://doi.org/10.1007/s00774-007-0810-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00774-007-0810-8

Key words

Navigation