Total glucosides of paeony suppresses adjuvant arthritis in rats and intervenes cytokine-signaling between different types of synoviocytes

被引:145
作者
Zheng, YQ [1 ]
Wei, W [1 ]
机构
[1] Anhui Med Univ, Inst Clin Pharmacol, Hefei 230032, Peoples R China
基金
中国国家自然科学基金;
关键词
adjuvant arthritis; fibroblast-like synoviocytes; macrophage-like synoviocytes; mitogen-activated protein kinases; total glucosides of paeony;
D O I
10.1016/j.intimp.2005.03.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Total glucosides of paeony (TGP) are active compounds extracted from the roots of Paeonia lactiflora Pall. In this study, we investigated the mechanisms of total glucosides of paeony (TGP) in the treatment of adjuvant arthritis (AA). AA in rats was established. Synoviocytes proliferation and activity of IL-1 were determined by 3-(4, 5-2dimethylthiazal-2yl) 2, 5-diphenylte-trazoliumbromide (MTT) assay. Tumor necrosis factor alpha (TNF-alpha) and prostaglandin E-2 (PGE(2)) were measured by radio immunoassay. Ultrastructure of synovioctes was observed under transmission electron microscope. Phosphorylation of c-Jun N-terminal kinase (JNK), extracellular regulating kinase (ERK) and p38 kinase and expression of matrix metalloproteinases (MMPs) were detected by Western blot analysis. TGP (25, 50 and 100 mg kg(-1), ig, days 14-21) inhibited secondary inflammatory reaction, bone destruction and ultrastructure change of synoviocytes in AA rats. The administration of TGP (50 and 100 mg/kg, ig, days 14-21) in AA rats significantly decreased the production of IL-1, PGE2 and TNF-a by macrophage-like synoviocytes (MLS). TGP (25 mg/kg) also decreased the production of PGE2 by MLS in AA rats. Furthermore, the increased phosphorylation of MAPKs, cell proliferation, and MMPs expression in fibroblast-like synoviocytes (FLS) stimulated by supernatants of MLS in AA rats could also be inhibited by TGP (50 and 100 mg/kg, ig, days 14-21). The results suggest that TGP possesses anti-inflammatory effects by modulating the pro-inflammatory mediators production from MLS and phosphorylation of MAPKs from FLS. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1560 / 1573
页数:14
相关论文
共 32 条
  • [11] GAO BB, 1996, ACAD J WEI FANG MAD, V18, P43
  • [12] Ge ZD., 1995, CHINESE PHARMACOL B, V11, P303, DOI [10.3321/j.issn:1001-1978.1995.04.012, DOI 10.3321/J.ISSN:1001-1978.1995.04.012]
  • [13] Hunter David, 2004, ACP J Club, V141, P69
  • [14] JUN L, 1995, CHINESE PHARM B, V11, P475
  • [15] Efficient FFT network testing and diagnosis schemes
    Li, JF
    Wu, CW
    [J]. IEEE TRANSACTIONS ON VERY LARGE SCALE INTEGRATION (VLSI) SYSTEMS, 2002, 10 (03) : 267 - 278
  • [16] Lu HS, 2000, CHINESE MED J-PEKING, V113, P872
  • [17] SYNOVIOCYTES SYNTHESIZE, BIND, AND RESPOND TO BASIC FIBROBLAST GROWTH-FACTOR
    MELNYK, VO
    SHIPLEY, GD
    STERNFELD, MD
    SHERMAN, L
    ROSENBAUM, JT
    [J]. ARTHRITIS AND RHEUMATISM, 1990, 33 (04): : 493 - 500
  • [18] Chemokines regulate IL-6 and IL-8 production by fibroblast-like synoviocytes from patients with rheumatoid arthritis
    Nanki, T
    Nagasaka, K
    Hayashida, K
    Saita, Y
    Miyasaka, N
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 167 (09) : 5381 - 5385
  • [19] Functional characterization of adherent synovial fluid cells in rheumatoid arthritis - Destructive potential in vitro and in vivo
    Neidhart, M
    Seemayer, CA
    Hummel, KM
    Michel, BA
    Gay, RE
    Gay, S
    [J]. ARTHRITIS AND RHEUMATISM, 2003, 48 (07): : 1873 - 1880
  • [20] Reimold A. M., 2002, Current Drug Targets - Inflammation and Allergy, V1, P377, DOI 10.2174/1568010023344535