Icariin isolated from Epimedium pubescens regulates osteoblasts anabolism through BMP-2, SMAD4, and Cbfa1 expression

被引:138
作者
Hsieh, Tsai-Pei [2 ]
Sheu, Shiow-Yunn [2 ]
Sun, Jui-Sheng [1 ,3 ,5 ,6 ]
Chen, Ming-Hong [4 ]
Liu, Man-Hai [2 ]
机构
[1] Natl Yang Ming Univ, Inst Clin Med, Taipei 11221, Taiwan
[2] Taipei Med Univ, Coll Pharm, Sch Pharm, Taipei 110, Taiwan
[3] Taipei Med Univ, Grad Inst Clin Med, Taipei 110, Taiwan
[4] Natl Yang Ming Univ, Inst Biomed Engn, Taipei 11221, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Orthoped Surg, Taipei, Taiwan
[6] Taipei Med Univ, Shuang Ho Hosp, Dept Orthoped Surg, Jhonghe City 235, Taipei County, Taiwan
关键词
Icariin; Osteoblast; Gene expression; BMP-2; SMAD4; Cbfa1; OPG; RANKL; NITRIC-OXIDE SYNTHASE; MARROW STROMAL CELLS; BONE-FORMATION; IN-VITRO; POSTMENOPAUSAL WOMEN; CONTROLLED TRIAL; DIFFERENTIATION; FLAVONOIDS; ESTROGEN; GROWTH;
D O I
10.1016/j.phymed.2009.08.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Epimedii herba is one of the most frequently used herbs in formulas prescribed for the treatment of osteoporosis in China The main active flavonoid glucoside extracted from Epimedium pubescens is Icariin, which has been reported to enhance bone healing and reduce osteoporosis occurrence. However, the detailed molecular mechanisms remain unclear In this present study, we examine the molecular mechanisms of icariin by using primary osteoblast cell cultures obtained from adult mice. The osteoblast cells were harvested from 8-month old female Imprinting Control Region (ICR) mice. The effects of icariin stimulation on the proliferation, differentiation and maturation of osteoblasts were examined. The production of nitric oxide (NO) and caspase-3 were analyzed, along with the gene expressions of bone morphogenetic protein-2 (BMP-2), SMAD4, Cbfa1/Runx2, OPG, and RANKL. The viability of the osteoblasts reached its maximum at 10(-8) M icariin. At this concentration, icariin increased the proliferation and matrix mineralization of osteoblasts and promoted NO synthesis With icariin treatment, the BMP-2, SMAD4, Cbfa1/Runx2, and OPG gene expressions were up-regulated, the RANKL gene expression was however down-regulated. Concurrent treatment involving the BMP antagonist (Noggin) or the NOS inhibitor (L-NAME) diminished the icariin-induced cell proliferation, ALP activity, NO production, as well as the BMP-2, SMAD4, Cbfa1/Runx2, OPG, RANKL gene expressions In this study, we demonstrate that in vitro icariin is a bone anabolic agent that may exert its osteogenic effects through the induction of BMP-2 and NO synthesis, subsequently regulating Cbfa1/Runx2, OPG, and RANKL gene expressions This effect may contribute to its action on the induction of osteoblasts proliferation and differentiation, resulting in bone formation. (C) 2009 Elsevier GmbH. All rights reserved
引用
收藏
页码:414 / 423
页数:10
相关论文
共 43 条
  • [1] Endothelial nitric oxide synthase in the control of osteoblastic mineralizing activity and bone integrity
    Afzal, F
    Polak, J
    Buttery, L
    [J]. JOURNAL OF PATHOLOGY, 2004, 202 (04) : 503 - 510
  • [2] Endothelial nitric oxide synthase gene-deficient mice demonstrate marked retardation in postnatal bone formation, reduced bone volume, and defects in osteoblast maturation and activity
    Aguirre, J
    Buttery, L
    O'Shaughnessy, M
    Afzal, F
    de Marticorena, IF
    Hukkanen, M
    Huang, P
    MacIntyre, I
    Polak, J
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (01) : 247 - 257
  • [3] An SJ, 2000, CHIN J OSTEOPOROSIS, V6, P55
  • [4] POLYPEPTIDE FACTORS REGULATING OSTEOGENESIS AND BONE-MARROW REPAIR
    BAB, IA
    EINHORN, TA
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 55 (03) : 358 - 365
  • [5] Bao Jia-rong, 2005, Wei Sheng Yan Jiu, V34, P191
  • [6] A review of clinical trials of therapies for osteoporosis using fracture as an end point
    Blank, RD
    Bockman, RS
    [J]. JOURNAL OF CLINICAL DENSITOMETRY, 1999, 2 (04) : 435 - 452
  • [7] Osteoclast differentiation and activation
    Boyle, WJ
    Simonet, WS
    Lacey, DL
    [J]. NATURE, 2003, 423 (6937) : 337 - 342
  • [8] Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton
    Brunet, LJ
    McMahon, JA
    McMahon, AP
    Harland, RM
    [J]. SCIENCE, 1998, 280 (5368) : 1455 - 1457
  • [9] Chen KM, 2005, PHARMAZIE, V60, P939
  • [10] Suppression of tumor necrosis factor-mediated apoptosis by nuclear factor κB-independent bone morphogenetic protein/Smad signaling
    Chen, SQ
    Guttridge, DC
    Tang, E
    Shi, ST
    Guan, KL
    Wang, CY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (42) : 39259 - 39263