Effect of bergenin on RANKL-induced osteoclast differentiation in the presence of methylglyoxal

被引:6
|
作者
Suh, Kwang Sik [1 ]
Chon, Suk [1 ]
Jung, Woon-Won [2 ]
Choi, Eun Mi [1 ]
机构
[1] Kyung Hee Univ, Sch Med, Dept Endocrinol & Metab, 1 Hoegi Dong, Seoul 02447, South Korea
[2] Cheongju Univ, Coll Hlth Sci, Dept Biomed Lab Sci, Cheongju 28503, Chungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Bergenin; Differentiation; Methylglyoxal; Osteoclast; NUCLEAR-FACTOR; GLYOXALASE I; KAPPA-B; BONE; ACTIVATION; CELLS; TRANSCRIPTION; CALCIUM; MECHANISMS; INDUCTION;
D O I
10.1016/j.tiv.2019.104613
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Methylglyoxal (MG), a highly reactive dicarbonyl compound, is a major precursor in the formation of advanced glycation end products, which are associated with diabetes-related diseases. Bergenin, an active constituent of plants of the genus Bergenia, exhibits multiple biological activities. This study evaluated the effect of bergenin on osteoclast differentiation and determined its mechanism of action. Bergenin reversed MG-inhibited tartrate-resistant acid phosphatase (TRAP) activity and decreased the bone resorption activity of osteoclasts. Quantitative RT-PCR revealed that bergenin decreased the expression of ERK1, Akt2, MMP-9, and OSTM1 genes in the presence of MG. Bergenin pretreatment yielded significant increases in intracellular calcium concentration, mitochondrial mass, mitochondrial membrane potential, and glyoxalase I reduced by MG. Additionally, bergenin decreased the formation of mitochondrial superoxide induced by MG. Detoxification of MG by bergenin may be a viable treatment for bone disorders in patients with diabetes.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Relationship between fluoride exposure and osteoclast markers during RANKL-induced osteoclast differentiation
    Pei Junrui
    Li Bingyun
    Gao Yanhui
    Xu, Jiaxun
    Darko, Gottfried M.
    Sun Dianjun
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2016, 46 : 241 - 245
  • [22] Humanin suppresses RANKL-induced osteoclast differentiation through AMPK activation
    Kang, Namju
    Kim, Ki Woo
    Shin, Dong Min
    JOURNAL OF BONE AND MINERAL RESEARCH, 2019, 34 : 234 - 234
  • [23] A novel organosulfur compound, thiacremonone, regulates RANKL-induced osteoclast differentiation
    Park, Kyung-Ran
    Kim, Ji-Youn
    Hong, Jin Tae
    Yun, Hyung-Mun
    RSC ADVANCES, 2017, 7 (49): : 30657 - 30662
  • [24] INTERLEUKIN 29 INHIBITS OSTEOCLAST DIFFERENTIATION AND FUNCTION IN RANKL-INDUCED OSTEOCLASTOGENESIS
    Wang, F.
    Luo, A.
    Wu, Q.
    Zhou, Z.
    Peng, Q.
    Xuan, W.
    Tan, W.
    ANNALS OF THE RHEUMATIC DISEASES, 2018, 77 : 881 - 881
  • [25] Cordyceps militaris Mushroom and Cordycepin Inhibit RANKL-Induced Osteoclast Differentiation
    Kim, Jinhee
    Lee, Hyejin
    Kang, Ki Sung
    Chun, Kwang-Hoon
    Hwang, Gwi Seo
    JOURNAL OF MEDICINAL FOOD, 2015, 18 (04) : 446 - 452
  • [26] Hydrogen peroxide as a regulator of RANKL-induced calcium oscillations and osteoclast differentiation
    Hong, J.
    Kim, M.
    Seo, J.
    Lee, S.
    Shin, D.
    CALCIFIED TISSUE INTERNATIONAL, 2007, 80 : S91 - S91
  • [27] D(-)-salicin inhibits RANKL-induced osteoclast differentiation and function in vitro
    Xiao, Yu
    Xian, Yansi
    Hu, Xinmei
    Qi, Zhongquan
    FITOTERAPIA, 2022, 157
  • [28] β-Glycerophosphate accelerates RANKL-induced osteoclast formation in the presence of ascorbic acid
    Noh, A. Long Sae Mi
    Yim, Mijung
    PHARMAZIE, 2011, 66 (03): : 195 - 200
  • [29] Hydrogen sulfide inhibits RANKL-induced ROS production and osteoclast differentiation
    Gambari, Laura
    Lisignoli, Gina
    Manferdini, Cristina
    Gabusi, Elena
    Piacentini, Anna
    Facchini, Andrea
    Grassi, Francesco
    NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2012, 27 : S28 - S28
  • [30] Pepstatin A, an aspartic proteinase inhibitor, suppresses RANKL-induced osteoclast differentiation
    Yoshida, H
    Okamoto, K
    Iwamoto, T
    Sakai, E
    Kanaoka, K
    Hu, JP
    Shibata, M
    Hotokezaka, H
    Nishishita, K
    Mizuno, A
    Kato, Y
    JOURNAL OF BIOCHEMISTRY, 2006, 139 (03): : 583 - 590