Paeoniflorin induced immune tolerance of mesenteric lymph node lymphocytes via enhancing beta 2-adrenergic receptor desensitization in rats with adjuvant arthritis

被引:126
作者
Wu, Hong
Wei, Wei [1 ]
Song, Lihua
Zhang, Lingling
Chen, Yin
Hu, Xiangyang
机构
[1] Anhui Med Univ, Inst Clin Pharmacol, Key Lab Antiinflammatoryimmunopharmacol Ahhui Pro, Key Lab Res & Dev Chinese Med Anhui Province, Hefei 230032, Anhui, Peoples R China
[2] Anhui Coll Tradit Chinese Med, Hefei 230031, Anhui Province, Peoples R China
[3] Anhui Med Univ, Dept Pathol, Hefei 230032, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
adjuvant arthritis; beta 2-adrenergic receptor; mesenteric lymph node lymphocytes; immune tolerance; paeoniflorin;
D O I
10.1016/j.intimp.2007.01.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Paeoniflorin (Pae), a monoterpene glucoside, is one of the main bioactive components of total glucosides of paeony (TGP) extracted from the root of Paeonia lactiflora. TGP has anti-inflammatory and immunoregulatory effects. In this study, we investigated the effects of Pae on inflammatory and immune responses to the mesenteric lymph node (MLN) lymphocytes and the mechanisms by which Pae regulates beta 2-adrenergic receptor (beta 2-AR) signal transduction in adjuvant arthritis (AA) rats. The onset of secondary arthritis in rats appeared around day 14 after injection of Freund's complete adjuvant (FCA). Remarkable secondary inflammatory response and lymphocytes proliferation were observed in AA rats, along with the decrease of anti-inflammatory cytokines interleukin (IL)-4 and transforming growth factor-beta 1 (TGF-beta 1) of MLN lymphocytes, and the increase of pro-inflammatory cytokine IL-2. The administration of Pae (50, 100 mg kg(-1), days 17-24) significantly diminished the secondary hind paw swelling and arthritis scores, reversed the changes of cytokines as discussed above, and further decreased the lowered proliferation of MLN lymphocytes in AA rats. In vitro, Pae restored the previously increased level of cAMP of MLN lymphocytes at the concentrations of 12.5, 62.5 and 312.5 mg 1(-1). Meanwhile, Pae increased protein expressions of beta 2-AR and GRK2, and decreased that of beta-arrestin 1, 2 of MLN lymphocytes in AA rats. These results suggested that Pae might induce the Th1 cells immune tolerance, which then shift to Th2, TO cells mediated activities to take effect the anti-inflammatory and immunoregulatory effects. The mechanisms of Pae on beta 2-AR desensitization and beta 2-AR-AC-cAMP transmembrane signal transduction of MLN lymphocytes play crucial roles in pathogenesis of this disease. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:662 / 673
页数:12
相关论文
共 54 条
[1]   PATIENT EMPOWERMENT - RESULTS OF A RANDOMIZED CONTROLLED TRIAL [J].
ANDERSON, RM ;
FUNNELL, MM ;
BUTLER, PM ;
ARNOLD, MS ;
FITZGERALD, JT ;
FESTE, CC .
DIABETES CARE, 1995, 18 (07) :943-949
[2]   INFLAMMATION ACTIVATES SELF HSP60-SPECIFIC T-CELLS [J].
ANDERTON, SM ;
VANDERZEE, R ;
GOODACRE, JA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (01) :33-38
[3]  
ANDERTON SM, 1994, J IMMUNOL, V152, P3656
[4]  
BLASI DA, 1995, J CLIN INVET, V95, P203
[5]  
CHUANG TT, 1992, J BIOL CHEM, V267, P6886
[6]   The β2-adrenergic agonist salbutamol potentiates oral induction of tolerance, suppressing adjuvant arthritis and antigen-specific immunity [J].
Cobelens, PM ;
Kavelaars, A ;
Vroon, A ;
Ringeling, M ;
van der Zee, R ;
van Eden, W ;
Heijnen, CJ .
JOURNAL OF IMMUNOLOGY, 2002, 169 (09) :5028-5035
[7]   Essential role for G protein-coupled receptor endocytosis in the activation of mitogen-activated protein kinase [J].
Daaka, Y ;
Luttrell, LM ;
Ahn, S ;
Della Rocca, GJ ;
Ferguson, SSG ;
Caron, MG ;
Lefkowitz, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (02) :685-688
[8]  
DAI Y, 2004, CELL STRESS CHAPERON, V9, P378
[9]   Stress hormones, proinflammatory and antiinflammatory cytokines, and autoimmunity [J].
Elenkov, IJ ;
Chrousos, GP .
NEUROENDOCRINE IMMUNE BASIS OF THE RHEUMATIC DISEASES II, PROCEEDINGS, 2002, 966 :290-303
[10]   Rheumatoid arthritis [J].
Feldmann, M ;
Brennan, FM ;
Maini, RN .
CELL, 1996, 85 (03) :307-310