Inhibitory Effect of Probenecid on Osteoclast Formation via JNK, ROS and COX-2

被引:16
作者
Cheng, Mi Hyun [1 ]
Kim, Sung-Jin [1 ]
机构
[1] Kyung Hee Univ, Sch Dent, Grad Sch, Dept Pharmacol & Toxicol, Seoul 02447, South Korea
关键词
Probenecid; Antiosteoclastogenesis; Oxidative stress; ROS; COX-2; JNK; PEROXIDE-INDUCED APOPTOSIS; ACTIVATED PROTEIN-KINASE; NECROSIS-FACTOR RECEPTOR; NF-KAPPA-B; HYDROGEN-PEROXIDE; REACTIVE OXYGEN; BONE-RESORPTION; DIFFERENTIATION; GENERATION; LIPOPOLYSACCHARIDE;
D O I
10.4062/biomolther.2019.047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Probenecid is a representative drug used in the treatment of gout. A recent study showed that probenecid effectively inhibits oxidative stress in neural cells. In the present study, we investigated whether probenecid can affect osteoclast formation through the inhibition of reactive oxygen species (ROS) formation in RAW264.7 cells. Lipopolysaccharide (LPS)-induced ROS levels were dose-dependently reduced by probenecid. Fluorescence microscopy analysis clearly showed that probenecid inhibits the generation of ROS. Western blot analysis indicated that probenecid affects two downstream signaling molecules of ROS, cyclooxygenase 2 (COX-2) and c-Jun N-terminal kinase (JNK). These results indicate that probenecid inhibits ROS generation and exerts antiosteoclastogenic activity by inhibiting the COX-2 and JNK pathways. These results suggest that probenecid could potentially be used as a therapeutic agent to prevent bone resorption.
引用
收藏
页码:104 / 109
页数:6
相关论文
共 45 条
  • [11] Redox signaling: thiol chemistry defines which reactive oxygen and nitrogen species can act as second messengers
    Forman, HJ
    Fukuto, JM
    Torres, M
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (02): : C246 - C256
  • [12] Hydrogen peroxide, but not superoxide, stimulates bone resorption in mouse calvariae
    Fraser, JHE
    Helfrich, MH
    Wallace, HM
    Ralston, SH
    [J]. BONE, 1996, 19 (03) : 223 - 226
  • [13] OXYGEN-DERIVED FREE-RADICALS STIMULATE OSTEOCLASTIC BONE-RESORPTION IN RODENT BONE INVITRO AND INVIVO
    GARRETT, IR
    BOYCE, BF
    OREFFO, ROC
    BONEWALD, L
    POSER, J
    MUNDY, GR
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (03) : 632 - 639
  • [14] Protection against titanium particle-induced osteoclastogenesis by cyclooxygenase-2 selective inhibitor
    Geng, D. C.
    Zhu, X. S.
    Mao, H. Q.
    Meng, B.
    Chen, L.
    Yang, H. L.
    Xu, Y. Z.
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2011, 99A (04) : 516 - 522
  • [15] Role of reactive oxygen species in bradykinin-induced mitogen-activated protein kinase and c-fos induction in vascular cells
    Greene, EL
    Velarde, V
    Jaffa, AA
    [J]. HYPERTENSION, 2000, 35 (04) : 942 - 947
  • [16] GUTMAN AB, 1951, B NEW YORK ACAD MED, V27, P144
  • [17] THE ROLE OF REACTIVE OXYGEN INTERMEDIATES IN OSTEOCLASTIC BONE-RESORPTION
    HALL, TJ
    SCHAEUBLIN, M
    JEKER, H
    FULLER, K
    CHAMBERS, TJ
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 207 (01) : 280 - 287
  • [18] Lipopolysaccharide (LPS) promotes osteoclast differentiation and activation by enhancing the MAPK pathway and COX-2 expression in RAW264.7 cells
    Hou, Guo-Qing
    Guo, Chun
    Song, Guo-Hua
    Fang, Na
    Fan, Wen-Juan
    Chen, Xu-Dong
    Yuan, Lei
    Wang, Zhen-Quan
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2013, 32 (02) : 503 - 510
  • [19] Upregulation of MKP-7 in response to rosiglitazone treatment ameliorates lipopolysaccharide-induced destabilization of SIRT1 by inactivating JNK
    Hwang, Jung Seok
    Ham, Sun Ah
    Yoo, Taesik
    Lee, Won Jin
    Paek, Kyung Shin
    Kim, Jae-Hwan
    Lee, Chi-Ho
    Seo, Han Geuk
    [J]. PHARMACOLOGICAL RESEARCH, 2016, 114 : 47 - 55
  • [20] Taurine exerts anti-osteoclastogenesis activity via inhibiting ROS generation, JNK phosphorylation and COX-2 expression in RAW264.7 cells
    Jang, Hae Jin
    Kim, Sung-Jin
    [J]. JOURNAL OF RECEPTORS AND SIGNAL TRANSDUCTION, 2013, 33 (06) : 387 - 391