期刊论文详细信息
BMC Complementary and Alternative Medicine
Lactobacillus fermentation enhances the inhibitory effect of Hwangryun-haedok-tang in an ovariectomy-induced bone loss
Jin Yeul Ma3  Dong-Hyun Seo1  Han Sung Kim1  Chang-Won Cho2  Kwang Jin Lee3  Hyunil Ha3  Taesoo Kim3  Ki-Shuk Shim3 
[1] Yonsei-Fraunhofer Medical Device Lab, Yonsei University, Wonju Gangwon, 220-710, South Korea;Regional Food Industry Research Group, Korea Food Research Institute, Sungnam 463-746, South Korea;KM-Based Herbal Drug Research Group, Korea Institute of Oriental Medicine, Daejeon 305-811, South Korea
关键词: Ovariectomy;    RANKL;    Osteoclastogenesis;    Lactobacillus curvatus;    Hwangryun-haedok-tang;   
Others  :  1229958
DOI  :  10.1186/1472-6882-13-106
 received in 2012-09-18, accepted in 2013-05-13,  发布年份 2013
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【 摘 要 】

Background

Hwangryun-haedok-tang (HRT) is traditional herbal medicine used to treat inflammatory-related diseases in Asia. However, its effect on osteoclastogenesis and bone loss is still unknown. In this study, we evaluated the effect of HRT and its fermented product (fHRT) on the receptor activator for the nuclear factor-κB ligand-induced osteoclastogenesis using murine bone marrow-derived macrophages and postmenopausal bone loss using an ovariectomy (OVX) rat model.

Methods

Tartrate resistant acid phosphatase (TRAP) staining was employed to evaluate osteoclast formation. mRNA level of transcription factor and protein levels of signaling molecules were determined by real-time quantitative polymerase chain reaction and Western blot analysis, respectively. Effect of HRT or fHRT on OVX-induced bone loss was evaluated using OVX rats orally administered HRT, or fHRT with 300 mg/kg for 12 weeks. Micro-CT analysis of femora was performed to analyze bone parameter.

Results

HRT or fHRT treatment significantly decreased TRAP activity and the number of TRAP positive multinuclear cells on osteoclastogenesis. Interestingly, these inhibitory effects of HRT were enhanced by fermentation. Furthermore, fHRT significantly inhibited mRNA and protein expression of nuclear factor of activated T cells cytoplasmic 1, which leads to down-regulation of NFATc1-regulated mRNA expressions such as TRAP, the d2 isoform of vacuolar ATPase V(0) domain, and cathepsin K. Administration of fHRT significantly inhibited the decrease of bone mineral density, and improved bone parameter of femora more than that of HRT and vehicle in OVX rats.

Conclusions

This study demonstrated that lactic bacterial fermentation fortifies the inhibitory effect of HRT on osteoclastogenesis and bone loss. These results suggest that fermented HRT might have the beneficial potential on osteoporosis by inhibiting osteoclastogenesis.

【 授权许可】

   
2013 Shim et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Canalis E, Giustina A, Bilezikian JP: Mechanisms of anabolic therapies for osteoporosis. N Engl J Med 2007, 357:905-916.
  • [2]Teitelbaum SL, Ross FP: Genetic regulation of osteoclast development and function. Nat Rev Genet 2003, 4:638-649.
  • [3]Prelevic GM, Kocjan T, Markou A: Hormone replacement therapy in postmenopausal women. Minerva Endocrinol 2005, 30:27-36.
  • [4]Davison S, Davis SR: Hormone replacement therapy: current controversies. Clin Endocrinol (Oxf) 2003, 58:249-261.
  • [5]Kronenberg F, Fugh-Berman A: Complementary and alternative medicine for menopausal symptoms: a review of randomized, controlled trials. Ann Intern Med 2002, 137:805-813.
  • [6]Putnam SE, Scutt AM, Bicknell K, Priestley CM, Williamson EM: Natural products as alternative treatments for metabolic bone disorders and for maintenance of bone health. Phytother Res 2007, 21:99-112.
  • [7]Boyle WJ, Simonet WS, Lacey DL: Osteoclast differentiation and activation. Nature 2003, 423:337-342.
  • [8]Takayanagi H: Osteoimmunology: shared mechanisms and crosstalk between the immune and bone systems. Nat Rev Immunol 2007, 7:292-304.
  • [9]Matsuo K, Galson DL, Zhao C, Peng L, Laplace C, Wang KZ, Bachler MA, Amano H, Aburatani H, Ishikawa H: Nuclear factor of activated T-cells (NFAT) rescues osteoclastogenesis in precursors lacking c-Fos. J Biol Chem 2004, 279:26475-26480.
  • [10]Zeng H, Dou S, Zhao J, Fan S, Yuan X, Zhu S, Li L, Zhang W, Liu R: The inhibitory activities of the components of Huang-Lian-Jie-Du-Tang (HLJDT) on eicosanoid generation via lipoxygenase pathway. J Ethnopharmacol 2011, 135:561-568.
  • [11]Choi HY, Kang BJ: Hanyakpoje ya Yimsangeumyoung. Seoul: Younglim-Sa; 2003.
  • [12]Ng CC, Wang CY, Wang YP, Tzeng WS, Shyu YT: Lactic acid bacterial fermentation on the production of functional antioxidant herbal Anoectochilus formosanus Hayata. J Biosci Bioeng 2011, 111:289-293.
  • [13]Lee HS, Kim MK, Kim YK, Jung EY, Park CS, Woo MJ, Lee SH, Kim JS, Suh HJ: Stimulation of osteoblastic differentiation and mineralization in MC3T3-E1 cells by antler and fermented antler using Cordyceps militaris. J Ethnopharmacol 2011, 133:710-717.
  • [14]Hsu MF, Chiang BH: Stimulating effects of Bacillus subtilis natto-fermented Radix astragali on hyaluronic acid production in human skin cells. J Ethnopharmacol 2009, 125:474-481.
  • [15]Kim T, Kim K, Lee SH, So HS, Lee J, Kim N, Choi Y: Identification of LRRc17 as a negative regulator of receptor activator of NF-kappaB ligand (RANKL)-induced osteoclast differentiation. J Biol Chem 2009, 284:15308-15316.
  • [16]Yamashita T, Yao Z, Li F, Zhang Q, Badell IR, Schwarz EM, Takeshita S, Wagner EF, Noda M, Matsuo K: NF-kappaB p50 and p52 regulate receptor activator of NF-kappaB ligand (RANKL) and tumor necrosis factor-induced osteoclast precursor differentiation by activating c-Fos and NFATc1. J Biol Chem 2007, 282:18245-18253.
  • [17]Kim HJ, Lee Y, Chang EJ, Kim HM, Hong SP, Lee ZH, Ryu J, Kim HH: Suppression of osteoclastogenesis by N, N-dimethyl-D-erythro-sphingosine: a sphingosine kinase inhibition-independent action. Mol Pharmacol 2007, 72:418-428.
  • [18]Yamamoto A, Miyazaki T, Kadono Y, Takayanagi H, Miura T, Nishina H, Katada T, Wakabayashi K, Oda H, Nakamura K: Possible involvement of IkappaB kinase 2 and MKK7 in osteoclastogenesis induced by receptor activator of nuclear factor kappaB ligand. J Bone Miner Res 2002, 17:612-621.
  • [19]Asagiri M, Sato K, Usami T, Ochi S, Nishina H, Yoshida H, Morita I, Wagner EF, Mak TW, Serfling E: Autoamplification of NFATc1 expression determines its essential role in bone homeostasis. J Exp Med 2005, 202:1261-1269.
  • [20]David JP, Sabapathy K, Hoffmann O, Idarraga MH, Wagner EF: JNK1 modulates osteoclastogenesis through both c-Jun phosphorylation-dependent and -independent mechanisms. J Cell Sci 2002, 115:4317-4325.
  • [21]Li X, Udagawa N, Itoh K, Suda K, Murase Y, Nishihara T, Suda T, Takahashi N: p38 MAPK-mediated signals are required for inducing osteoclast differentiation but not for osteoclast function. Endocrinology 2002, 143:3105-3113.
  • [22]Toda T, Uesugi T, Hirai K, Nukaya H, Tsuji K, Ishida H: New 6-O-acyl isoflavone glycosides from soybeans fermented with Bacillus subtilis (natto). I. 6-O-succinylated isoflavone glycosides and their preventive effects on bone loss in ovariectomized rats fed a calcium-deficient diet. Bio Pharm Bull 1999, 22:1193-1201.
  • [23]Matsubara M, Yamachika E, Tsujigiwa H, Mizukawa N, Ueno T, Murakami J, Ishida N, Kaneda Y, Shirasu N, Takagi S: Suppressive effects of 1,4-dihydroxy-2-naphthoic acid administration on bone resorption. Osteoporos Int 2010, 21:1437-1447.
  • [24]Narva M, Halleen J, Vaananen K, Korpela R: Effects of Lactobacillus helveticus fermented milk on bone cells in vitro. Life Sci 2004, 75:1727-1734.
  • [25]Scalbert A, Williamson G: Dietary intake and bioavailability of polyphenols. J Nutr 2000, 130:2073S-2085S.
  • [26]Izumi T, Piskula MK, Osawa S, Obata A, Tobe K, Saito M, Kataoka S, Kubota Y, Kikuchi M: Soy isoflavone aglycones are absorbed faster and in higher amounts than their glucosides in humans. J Nutr 2000, 130:1695-1699.
  • [27]Hendrich S: Bioavailability of isoflavones. J Chromatogr B Anal Technol Biomed Life Sci 2002, 777:203-210.
  • [28]Scholz-Ahrens KE, Ade P, Marten B, Weber P, Timm W, Acil Y, Gluer CC, Schrezenmeir J: Prebiotics, probiotics, and synbiotics affect mineral absorption, bone mineral content, and bone structure. J Nutr 2007, 137:838S-846S.
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