Effects and mechanisms of Geniposide on rats with adjuvant arthritis
Effects and mechanisms of Geniposide on rats with adjuvant arthritis
复制标题
京尼平苷对大鼠佐剂性关节炎的作用及机制
DOI：
10.1016/j.intimp.2014.02.021
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发表时间：
2014-05-01
影响因子：
5.6
通讯作者：
Shen, Chen
中科院分区：
文献类型：
--
作者：
Dai, Miao-Miao;Wu, Hong;Shen, Chen
Geniposide (GE), an iridoid glycoside compound, is the major active ingredient of Gardenia jasminoides Ellis (GJ) fruit which has anti-inflammatory and other important therapeutic activities. The aim of this study was to investigate the effects of GE on adjuvant arthritis (AA) rats and its possible mechanisms. AA was induced by injecting with Freund's complete adjuvant (FCA). Male SD rats were subjected to treatment with GE at 30, 60 and 120 mg/kg from days 18 to 24 after immunization. Lymphocyte proliferation was assessed by MIT. Interleukin (IL)-6, IL-17, IL-4 and transforming growth factor-beta 1 (TGF-beta(1)) were determined by ELISA. c-Jun N-terminal kinase (JNK) and phospho-JNK (p-JNK) were detected by Western blot. GE (60, 120 mg/kg) significantly relieved the secondary hind paw swelling and arthritis index, along with decreased Th17-cells cytokines and increased Treg-cell cytokines in mesenteric lymph node lymphocytes (MLNL) and peripheral blood lymphocytes (PBL) of AA rats. In addition, GE decreased the expression of p-JNK in MLNL and PBL of AA rats. In vivo study, it was also observed that GE attenuated histopathologic changes of MLN in AA rats. Collectively. GE might exert its anti-inflammatory and immunoregulatory effects through inducing Th17 cell immune tolerance and enhancing Treg cell-mediated activities by down-regulating the expression of p-JNK. The mechanisms of GE on JNK signaling in MLNL and PBL may play critical roles in the pathogenesis of rheumatoid arthritis. (C) 2014 Elsevier B.V. All rights reserved.
