基于胆碱能抗炎通路的艾灸治疗实验性RA作用机制研究
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摘要
目的:
     本研究依据“艾灸治疗RA抗炎效应明确,胆碱能抗炎通路对全身和局部炎症均具有明显的抑制作用”的基本事实,以针灸理论为指导,艾灸家兔“肾俞”、“足三里”治疗实验性RA,围绕滑膜炎症关键病理环节,选择胆碱能抗炎通路作为研究切入点,以“艾灸刺激一胆碱能抗炎通路一抗炎效应”为研究主线,运用神经阻断、免疫组化、实时荧光定量PCR等方法技术,探索胆碱能抗炎通路在艾灸治疗RA抗炎效应中的作用机制,对于深化艾灸治疗RA的原理研究、丰富灸法的科学内涵具有重要的价值和意义。
     方法:
     将日本大耳白兔随机分为正常对照组、RA模型组、艾灸治疗组、艾灸治疗迷走神经切断组、艾灸治疗假手术组,用福氏完全佐剂塑造RA疾病模型,运用颈部左侧迷走神经干切断术作为干预手段,艾灸“肾俞”、“足三里”治疗。1.观察RA家兔的整体状况、体重、膝关节周长、滑膜组织炎症病理形态;2.采用Elisa法检测滑膜液中TNF-α、IL-1、IL-6、HMGB1含量;3.采用Elisa法检测血清中a7nAChR和ChAT的含量;分别采用免疫组化法和实时荧光定量PCR法检测滑膜组织中a7nAChR、ChAT的蛋白表达和mRNA表达。4.采用免疫组化法检测滑膜组织中NF-κBp65、NF-κBp50、IκBα、IKKβ的表达。
     结果:
     1.艾灸家兔“肾俞”、“足三里”可以明显改善RA家兔全身状况、膝关节肿胀、关节滑膜炎症病理变化,而在切断迷走神经的情况下其作用显著降低。
     2.滑膜液中细胞因子检测结果显示:模型组与正常对照组相比较,RA模型组关节滑膜液中TNFα、IL-1、IL-6、HMGB1含量显著增高(P<0.01);与RA模型组比较,艾灸治疗组、艾灸治疗假手术组关节滑膜液中TNFα、IL-1、IL-6、 HMGB1含量显著降低(P<0.01),而艾灸治疗迷走神经切断组无明显降低((P>0.05);与艾灸治疗组比较,艾灸治疗迷走神经切断组滑膜液中TNFα、IL-1、 IL-6、HMGB1含量显著增高(P<0.01),但艾灸治疗假手术组无明显增高(P>0.05)。
     3.α7nAChR、ChAT表达结果显示:模型组与正常对照组相比较,模型组血清中α7nAChR、ChAT含量、滑膜组织中α7nAChR、ChAT蛋白表达和mRNA表达均显著降低(P<0.01);与模型组比较,艾灸组和假手术组血清中α7nAChR、 ChAT含量、滑膜组织中α7nAChR、ChAT蛋白表达和mRNA表达均显著增高(P<0.01),而艾灸治疗迷走神经切断组无明显增高(P>0.05);与艾灸组比较,艾灸治疗迷走神经切断组血清中α7nAChR、ChAT含量、滑膜组织中α7nAChR、ChAT蛋白表达和mRNA表达均显著降低(P<0.01),但假手术组无明显降低(P>0.05)。
     4.①NF-κBp65、NF-κBp50、p-IκBα、IKKβ表达结果显示:模型组与正常对照组相比较,模型组滑膜组织中NF-κBp65、NF-κBp50、p-IκBα、IKKβ的表达显著增高(P<0.01);与模型组比较,艾灸组和假手术组滑膜组织中NF-κBp65、 NF-KBp50、p-IκBα、IKKβ的表达显著降低(P<0.01),而艾灸治疗迷走神经切断组无明显降低(P>0.05);与艾灸组比较,艾灸治疗迷走神经切断组滑膜组织中NF-KBp65、NF-κBp50、p-IKBα、IKKβ的表达显著增高(P<0.01),但假手术组无明显增高(P>0.05)。
     ②IκBα表达结果显示:模型组与正常对照组相比较,模型组滑膜组织中IκBα的表达显著降低(P<0.01);与模型组比较,艾灸组和假手术组滑膜组织中IκBα的表达显著增高(P<0.01),而艾灸治疗迷走神经切断组无明显增高(P>0.05);与艾灸组比较,艾灸治疗迷走神经切断组滑膜组织中IκBα的表达显著降低(P<0.01),但假手术组无明显降低(P>0.05)。
     结论:
     1.艾灸家兔“肾俞”、“足三里”可以明显改善实验性RA家兔全身状况、膝关节肿胀、关节滑膜炎症病理变化,表明艾灸具有明确的抗炎消肿、抑制滑膜炎症作用,而在切断迷走神经的情况下其抗炎作用显著降低,提示艾灸治疗RA的抗炎效应可能与兴奋胆碱能抗炎通路密切相关。
     2.艾灸家兔“肾俞”、“足三里”可以抑制实验性RA家兔滑膜液中细胞因子TNF-α、IL-1、IL-6和HMGB1水平,但在切断迷走神经的情况下其作用显著下降,提示兴奋胆碱能抗炎通路可能是艾灸抑制实验性RA家兔滑膜细胞分泌促炎细胞因子的重要机制之一。
     3.艾灸家兔“肾俞”、“足三里”可以上调ChAT在RA家兔外周血和滑膜组织中的表达,激活免疫系统的固有胆碱能系统,但在切断迷走神经的情况下其作用显著降低,提示艾灸可能通过兴奋迷走神经释放ACh,并与免疫细胞表面的a7nAChR结合,从而激活免疫细胞的固有胆碱能系统,转化为免疫系统内弥散的、持续的免疫调节。
     4.艾灸家兔“肾俞”、“足三里”可以抑制RA家兔滑膜组织中NF-κBp65、 NF-κBp50、p-IκBα、IKKβ的蛋白表达,上调IκBα的蛋白表达,但在切断迷走神经的情况下其作用显著降低,因此推测艾灸可能通过抑制IKK/IκB/NF-κB信号转导通路活化,改善RA家兔滑膜NF-κB的高调控状态,抑制滑膜细胞炎性细胞因子和炎性介质的合成和分泌,从而实现其抗炎效应,胆碱能抗炎通路在其中具有重要作用。
Objective:
     The research is based on the fact that "moxibustion has obvious anti-inflammatory effects of treating RA and cholinergic anti-inflammatory pathway can obviously inhibit systemic and local inflammation ". Guided by the theory of acupuncture and moxibustion, experimental RA rabbits were treated by moxibustion at "Shenshu"" Zusanli"points. Focusing on the key pathological character of synovitis, we selected cholinergic anti-inflammatory pathway as the breakthrough point of the research and "moxibustion stimulation-cholinergic anti-inflammatory pathway-anti-inflammatory effecf" as the main line of the research. By the use of nerve block, immunohistochemistry, RT-PCR and other methods and techniques, to explore cholinergic anti-inflammatory pathway's mechanism of action in treating RA by moxibustion, the research is of important value for deepening the study of the principles of moxibustion treatment of RA and enriching scientific connotation of moxibustion.
     Methods:
     Japanese big-eared white rabbits were randomly divided into normal control group, RA model group, moxibustion treatment group, normal treatment of vagotomy group, moxibustion treatment of sham operation group. RA animal models were produced by Freunds1Complete Adjuvant (FCA) and left truncal vagotomy of the neck was as a means of intervention. RA rabbits were treated by moxibustion at "Shenshu"" Zusanli"points.1. RA rabbits'overall condition, body weight, knee joint perimeter, pathological morphology of synovial membrane tissue inflammation were observed.2. TNF-a, IL-1, IL-6, HMGB1in synovial fluid were detected by enzyme-linked immunosorbent assay (ELISA).3.Content of α7nAChR, ChAT in blood serum were detected by enzyme-linked immunosorbent assay (ELISA). Expression of a7nAChR, ChAT in synovial membrane tissue were detected by immunohistochemistry method and mRNA expression of a7nAChR, ChAT in synovial membrane tissue were detected by RT-PCR method.4. Expression of NF-KBp65, NF-κBp50, IκBα, p-IκBa, IKKβ in synovial membrane tissue were detected by immunohistochemistry method.
     Results:
     1. Moxibustion at "Shenshu" and "Zusanli" points of rabbits could obviously improve RA rabbits" overall condition, body weight, knee joint perimeter, pathological morphology of synovial membrane tissue inflammation, but its effect was decreased significantly after cutting off the vagus nerve.
     2. The expression results of cytokine in synovial fluid showed:Compared with the normal control group, RA model group's expression of TNF a, IL-1, IL-6, HMGB1in synovial fluid were significantly increased (P<0.01); Compared with model group, moxibustion group and sham operation group were decreased significantly (P<0.01) and vagotomy group was not decreased significantly (P>0.05); Compared with moxibustion group, vagotomy group were significantly increased (P<0.01), but the sham operation group was not significantly increased (P>0.05).
     3. The expression results of a7nAChR and ChAT showed:Compared with the normal control group, RA model group's expression of α7nAChR, ChAT in blood serum and proteinum expression of α7nAChR, ChAT in synovial membrane tissue mRNA expression of a7nAChR, ChAT in synovial membrane tissue were decreased significantly (P<0.01); Compared with model group, moxibustion group and sham operation group's expression of a7nAChR, ChAT in blood serum and proteinum expression of a7nAChR, ChAT in synovial membrane tissue mRNA expression of a7nAChR, ChAT in synovial membrane tissue were significantly increased (P<0.01) and vagotomy group was not increased significantly (P>0.05); Compared with moxibustion group, vagotomy group were significantly decreased (P<0.01), but the sham operation group was not significantly decreased (P>0.05).
     4.①The expression results of NF-κBp65, NF-κBp50, p-IκBα, IKKα showed: Compared with the normal control group, RA model group's expression of NF-κBp65, NF-κBp50, p-IκBα, IKKP in synovial membrane tissue were significantly increased (P<0.01); Compared with model group, moxibustion group and sham operation group's expression of NF-κBp65, NF-KBp50, p-IκBα, IKKP in synovial membrane tissue were decreased significantly (P<0.01) and vagotomy group was not decreased significantly (P>0.05); Compared with moxibustion group, vagotomy group were significantly increased (P<0.01), but the sham operation group was not significantly increased (P>0.05).
     ②The expression results of IκBα showed:Compared with the normal control group, RA model group's expression of IκBαin synovial membrane tissue were significantly decreased (P<0.01); Compared with model group, moxibustion group and sham operation group's expression of IκBα in synovial membrane tissue were increased significantly (P<0.01) and vagotomy group was not increased significantly (P>0.05); Compared with moxibustion group, vagotomy group were significantly decreased (P<0.01), but the sham operation group was not significantly decreased (P>0.05).
     Conclusions:
     1. Moxibustion at "Shenshu" and "Zusanli" points of rabbits can obviously improve RA rabbits'overall condition, knee joint perimeter,pathological morphology of synovial membrane tissue inflammation,which shows that moxibustion has a definite effect of anti-inflammatory, detumescence and inhibition of synovial inflammation. But its effect is decreased significantly after cutting off the vagus nerve. It prompts that anti-inflammatory effect of moxibustion for treatment of RA may be closely related to stimulating cholinergic anti-inflammatory pathway.
     2. Moxibustion at "Shenshu" and "Zusanli" points of rabbits can inhibit expression of TNF a, IL-1, IL-6, HMGB1in synovial fluid of RA rabbits, but its effect is decreased significantly after cutting off the vagus nerve. It prompts that stimulating cholinergic anti-inflammatory pathway may be one of the important mechanisms that moxibustion inhibit expression of proinflammatory cytokines in synovial fluid of experimental RA rabbits.
     3.Moxibustion at "Shenshu" and "Zusanli" points of rabbits can increase the expression of a7nAChR、ChAT in blood serum and synovial membrane tissue of RA rabbits, and activate the inherent cholinergic system in immune system, but its effect is decreased significantly after cutting off the vagus nerve. It prompts that moxibustion may promote the vagus nerve to release ACh and make ACh combine with a7nAChR of immune cells, thereby activating the inherent cholinergic system in immune cells and converting to diffuse, sustained immune regulation within the immune system.
     4. Moxibustion at "Shenshu" and "Zusanli" points of rabbits can inhibit the expression of NF-κBp65、NF-icBp50、p-IκBα、IKKP in synovial membrane tissue of RA rabbits,and increase the expression of IicBa, but its effect is decreased significantly after cutting off the vagus nerve. Therefore we speculate that by inhibiting the activation of IKK/IκB/NF-κB signal transduction pathway moxibustion may restrain high regulation of NF-κB in RA rabbits'synovium and inhibit the expression of Inflammatory cytokines in synovial cells, and then achieve its anti-inflammatory effect, in which cholinergic anti-inflammatory pathway plays an important role.
引文
[1]Andcrsson, J. The inflammatory reflex-introduction[J]. Intern Med,2005,257(2):122-125.
    [2]张铃铃,沈玉先.类风湿关节炎的关节滑膜病理生理机制[J].生理科学进展,2003,34(2): 144.
    [3]戴敏,魏伟.类风湿关节炎滑膜细胞信号转导机制研究进展[J].中国药理学通报,2003,19(5):481-485.
    [4]李健武,刘建民,等.隔物温和灸配合西药治疗类风湿性关节炎临床观察[J].中国针灸,2006,26(3):192.
    [5]唐照亮,宋小鸽,陈全珠,等.艾灸抗炎免疫作用及对神经递质影响的实验研究[J]-中国中医基础医学杂志,2000,6(9):53.
    [6]唐照亮,宋鸽,侯正明,等.大鼠海马内微量注射6掘多巴胺对艾灸抗炎免疫作用的影响[J].针刺研究,2000,25(3):184.
    [7]唐照亮,宋小鸽,侯正明,等.艾灸抗炎与免疫作用的基础实验研究[J].针刺研究,1997,22(3): 168.
    [8]杨慎峭,刘旭光,余曙光,等.艾灸对类风湿性关节炎家兔关节滑膜液IL-1β、TNFa含量的影响[J].成都中医药大学学报,2005,28(3):11-12.
    [9]刘旭光杨慎峭 余曙光,等.艾灸对实验性类风湿性关节炎家兔关节滑膜液MMP-3. TIMP-1含量的影响[J].成都中医药大学学报,2005,28(4):1-2.
    [1 0]余俊辉,刘旭光,余曙光,等.艾灸对实验性类风湿关节炎滑膜细胞原癌基因c-fos和c-myc mRNA表达的影响[J].西部医学,2005,17(2):108-110.
    [11]刘旭光,房紧恭,余曙光,等,艾灸对实验性RA家兔关节滑膜液FGF EGF PDGF含量的影响[J].中医药学刊,2006,24(3):428-429.
    [12]周海燕,刘旭光,等.艾灸调整实验性RA大鼠HPAA功能的GR机制研究[J].中华中医药学刊,2010,28(6):1167-1169.
    [13]刘旭光,周海燕,黄迪君,等.艾灸对实验性RA大鼠海马下丘脑垂体GR表达影响的研[J].中华中医药学刊,2009,27(9):1797-1799.
    [14]Ulloa, L. The vagus nerve and the nicotinic anti-inflammatory pathway[J]. Nat ReV Drug Discov,2005,4(8):673-684.
    [15]Czura CJ, Friedman SG, Tracey KJ. Neural inhibition of inflammation:the cholinergic anti-inflammatory pathway [J]. Endotoxin Res,2003,9(6):409-413.
    [16]Van Maanen MA, Lebre MC, van der Poll T, et al. Stimulation of nicotinic acetylcholine receptors attenuates collagen-induced arthritis in mice[J]. Arthritis Rheum,2009,60(1): 114-122.
    [17]Li T, Zuo X, Zhou Y, et al. The vagus nerve and nicotinic receptors involve inhibition of HMGB 1 release and early pro-inflammatory cytokines function in collagen-induced arthritis[J]. Journal of clinical immunology,2010,30(2):213-220.
    [18]苏跃.胆碱能抗炎通路对家兔肺缺血再灌注损伤的影响[D].北京:北京市结核病胸部肿瘤研究所,2007,12-13.
    [19]Van Maanen MA, Vervoordeldonk MJ, Paul P Tak. The cholinergic anti-inflammatory pathway:towards innovative treatment of rheumatoid arthritis[J]. Nat Rev Rheumatol,2009, 5:229-232.
    [20]陈奇.中药药理实验方法学[M].北京:人民卫生出版社,1994,68.
    [21]Gay S, et al. Molecular and cellular mechanisms of joint destrution in rheumatoid arthritis: two cellular mechanisms explain joint destruction? [J]. Ann Rheum Dis,1993.52:39.
    [22]Firestein GS.Evolving concepts of rheumatoid arthritis[J].Nature,2003,423(6937):356-361.
    [23]TerlmanH, PagliariLJ, LiuH, etal. Rheumatoid arthritis synovial macrophages express the Fas-associated death domain-like interleukin-1B-converting enzyme-Inhibitory protein and are r fractory to Fas-Mediated apoptosis[J]. Arthritis rheum,2001,44:21-30.
    [24]陈桂敏,代林刚,贺金,等.类风湿性关节炎相关机制研究进展[J].海南医学院学报,2007,13(3):292-298.
    [25]Muller-Ladner U, et al. Activation of synoviocytes[J]. Curr Opin Rheumabol,2000,12:186.
    [26]Raimund W Kinne, et al. Activation of synovial fibroblast in rheumatoid arthritis[J].Annals of the Rheumatic Diseases,1995,54:501.
    [27]Ulf Muller-Ladner, et al. synovial fibroblasts of patients with rheumatoid arthritis attach to and invade normal human cartilage when engrafted into SCID mice.1996,149(5):1607
    [28]Keller, K et al. Effects of isolated rheumatoid synovial cells on cartilage degradation in vitro[J]. Orthop Res,1990.8:345.
    [29]Firestein, GS. Mechanisms of tissue destruction and cellular activation in rheumatoid arthritis[J]. Curr Opin Rheumatol.1992,4:348.
    [30]Trabandt A, et al. Expression of the collagenolytic and ras-induced cysteine proteinase cathepsin L and proliferation-associated oncogenes in synovial cells of MRL/1 mice and patients with rheumatoid arthritis[J]. Matrix,1990,10:349.
    [31]Zvaifler NJ, et al. Pannus and pannocytes.Alternative models of joint destruction in rheumatoid arthritis[J]. Arthritis Rheum.1994,37:783.
    [32]Kinne R W, et al. Expression of jun-B and c-fos proto-oncogenes by activated fibroblast-like cells in synovial tissue of rheumatoid arthritis and osteoarthritis patients[J]. Arthritis Rheum, 1993,36:264
    [33]Fox D A, et al. Activation pathways of synovial T lymphocytes[J]. Clin Invest,1990,86:1124.
    [34]Sivalingam SP,Thumboo J, Vasoo S, et al. In vivo pro-and anti-inflammatory cytokines in normal and patients with rheumatoid arthritis[J]. Ann Acad Med Singapore,2007,36(2):96-99.
    [35]Miossec P.An update on the cytokine network in rheumatoid arthritis[J]. Curropin Rheumatol.2004,16(3):218-222.
    [36]费克香,晏年春.类风湿性关节炎与T淋巴细胞研究[J].旧本医学介绍,2000,2l(9):427.
    [37]李霞,孙健,范成明.细胞因子与类凤湿关节炎[J].大连大学学报,2000,21(4):102.
    [38]Firestein GS. Evolving concepts of rheumatoid arthritis[J]. Nature.2003,423(6937):356-361.
    [39]张玲玲,沈玉先,魏伟.类风湿关节炎的关节滑膜病理生理机制[J].生理科学进展,2003,34(2): 146.
    [40]张义浜.类风湿关节炎发病机制及其治疗方法研究进展[J].细胞与分子免疫学杂志,2005,21(1):88.
    [41]HangHG,WangYM, XieJF, etal. Regulation of tumor necrosis factorA-mediated apoptosis of rheumatoid arthritis synovial fibroblasts by the protein kinase Akt[J]. Arthritis rheum, 2001,44:1555-1567.
    [42]Malemud CJ, Miller AH. Pro-inflammatory cytokine-induced SAPK/MAPK and JAK/STAT,in rheumatoid arthritis and the new anti-depression drugs[J]. ExPert OPin TherTargets,2008,12(2):171-183.
    [43]Olse N. Anti-TNF switehing:effect on outcomes in Patients with RA[J]. Nat Clin Pract Rheumatol,2007,3(8):430-431.
    [44]Muller-Ladner U, Gay RE, Gay5. Role of nuclear factor kappB in synovial inflammation[J]. Curreumatol ReP,2002,4(3):201-207.
    [45]Kubo M, Hanada T, Yoshimura A. Suppressors of cytokine signaling and immunity[J].Nat Immunol,2003,4(12):1169-1176.
    [46]Wendling D. Do patients with RA receiving anti-TNFagent have an increased risk of surgical site Infections? [J]. Nat Clin Pract Rheumatol,2007,3(8):432-433.
    [47]Tak PP, Firestein GS. NF-kappaB:a key role in inflammatory diseases[J]. Clin Invest.2001. 107(1):7-11.
    [48]TaylorPC. Is abatacept an effective treatmeat for Patients with RA who do not respond to other anti-TNF treatments? [J]. Nat Clin Pract Rheumatol,2006,2(3):128-129.
    [49]Askling J, Fored CM, Brandi L, et al. Time-dependent increase in risk of hospitalization with infection among Swedish RA Patients treated with TNF antagonists [J]. Ann Rheum Dis, 2007,66(10):1339-1344.
    [50]Georganas C, Liu H, Periman H, et al. Regulation of IL-6 and IL-8expression in rheumatoid arthritis synovial fibroblasts:the dominant role for NF-kappa B but notC/EBP beta or c-Jun[J]. Immunol,2006,165(12):7199-7206.
    [51]Aupperie KR, Bennett BL, Boyle DL, et al. NF-kappaB regulation by lkappaB kinase in primary fibroblast-like synoviocytes [J]. Immunol,1999,163(1):427-33.
    [52]Kisseleva T, Bhattacharya S, Braunstein J, et al. Signaling through the JAK/STAT pathway, recent advances and future challenges[J]. Gene,2002,285(1-2):1-24.
    [53]Ulloa, L. The vagus nerve and the nicotinic anti-inflammatory pathway [J]. Nat ReV Drug Discov,2005,4(8):673-684.
    [54]Tracey KJ.The inflammatory reflex[J]. Nature,2002,420:853-859.
    [55]Hong Wang,ManYu,Mahendar Ochani,etal. Nicotinic acetylcholine receptor a7 subunit is an essential regulator of inflammation[J]. Nature,2003,421(6921):384-388.
    [56]WANG Bo-jie, SU Yue. Development of research on cholinergic anti-inflammatory Pathway [J]. Anesth Resus,2006,27(4),242-245.
    [57]Czura CJ, Friedman SG, Tracey KJ. Neural inhibition of inflammation:the cholinergic anti-inflammatory pathway [J]. Endotoxin Res,2003,9(6):409-413.
    [58]Rosas-Ballina M, Tracey K J. Cholinergic control of inflammation[J]. Journal of Internal Medicine,2009,265:663.
    [59]Tracey K J. Physiology and immunology of the cholinergic anti-inflammatory pathway[J]. Clin Invest,,2007,117(2):289-296.
    [60]Wang H, Liao H, Ochani M et al. Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis[J]. Nat Med,2004,10(11):1216-1221.
    [61]王敏,孙炳伟.炎症反应调控新机制--神经系统胆碱能抗炎通路的调节作用[J].江苏大学学报,2010,20(3):274-276.
    [62]Guarini S, Altavilla D, Cainazzo MM, et al. Efferent vagal fibre stimulation blunts nuclear factor-kappaB activation and protects against hypovolemic hemorrhagic shock[J]. Circulation,2003,107(8):1189-1194.
    [63]Li, Q, and Verma, I.M.. NF-kappaB regulation in the immune system[J]. Nat Rev Immunol, 2002,2(10):725-734.
    [64]Wang. H., Liao, H., Ochani, M., et al. Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis[J]. Nat Med,2004,10(11):1216-1221.
    [65]Saeed, R.W.,Varma, S., Peng-Nemeroff, T., et al. Cholinergic stimulation blocks endothelial cell activation and leukocyte recruitment during inflammation[J]. Exp Med, 2005,201(7):1113-1123.
    [66]Hamano R, Takahashi HK, Lwagaki H, et al. Stimulation of alpha7 nicotinic acetylcholine receptor inhibits CD14 and the toll-like receptor4 expression in human monocytes[J].Shock, 2006,26(4):358-364.
    [67]Guha, M., O, Connell, M.A., Pawlinski, R., et al. LIpopolysaccharide activation of the MEK-ERK1/2 Pathway in human monoeytic cells mediates tissue factor and tumor necrosis factor alpha expression by inducing Elk-1 phosphorylation and Egr-1 expression[J]. Blood,2001,98(5):1429-1439.
    [68]De Jonge WJ, van der Zanden EP, The FO, Bijlsma MF, van Westerloo DJ, Bennink RJ, Berthoud HR, et al. Stimulation of the vagus nerve attenuates macrophage activation by activating the Jak2-STAT3 signaling pathway [J]. Nat Inununol,2005,6(8):844-851.
    [69]Chatterjee PK, AI-Abed Y, Sherry B, Metz CN. Cholinergic agonists regulate JAK2/STAT3 signaling to suppress endothelial cell activation [J]. Am J Physiol Cell Physiol,2009, 297(5):C1294-C1306.
    [70]Kubo, M.,Hanada, T., and Yoshimura, A. Suppressors of cytokine signaling and immunity[J]. Nat Immunol,2003,4(12):1169-1176.
    [71 Wittebole X, Hahm S, Coyle SM, et al. Nicotine exposure alters in vivo human responses to endotoxin[J]. Clin Exp Immunol 2007;147(1):28-34.
    [72]Pavlov VA, Ochani M, Gallowitsch-Puerta M, et al. Central muscarinic cholinergic regulation of the systemic inflammatory response during endotoxemia[J]. Proe Natl Acad Sci USA,2006,103(13):5219-5223.
    [73]Huston JM, Ochani M, Rosas-Ballina M, et al. Splenectomy inactivates the cholinergic anti-inflammatory pathway during lethal endotoxemia and polymicrobial sepsis[J]. Exp Med,2006,203(7):1623-1628.
    [74]Wang H, Liao H, Ochani M et al. Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis[J]. Nat Med,2004,10(11):1216-1221.
    [75]Guarini S, Cainazzo MM, Giuliani D, et al. Adrenocorticotropin reverses hemorrhagic shock in anesthetized rats through the rapid activation of a vagal anti-inflammatory pathway[J]. Cardiovasc Res,2004,63(2):357-365.
    [76]Guarini S, Altavilla D, Cainazzo MM et al. Efferent vagal fibre stimulation blunts nuclear factor-kappaB activation and protects against hypovolemic hemorrhagic shock[J]. Circulation 2003,107(8):1189-1194.
    [77]Bemik TR Friedman SG, Ochani M, et al. Cholinergic anti-inflammatory pathway inhibition of tumor necrosis factor during ischemia reperfusion[J]. Vase Stag,2002,36(6): 1231-1236.
    [78]Crockett ET, Galligan JJ, Uhal BD, et al. Protection of early phase hepatic ischemia-reperfusion injury by cholinergic agonists[J]. BMC Clin Pathol,2006,63.
    [79]Sadis C, Teske G Stokman G, et al. Nicotine protects kidney from renal ischemia reperfusion injury through the cholinergic anti-inflammatory pathway[J]. PLoS One,2007,2(5):469.
    [80]Van Westerloo DJ, Giebelen IA,Florquin S, et al.The cholinergic anti-inflammatory pathway regulates the host response during septic peritonitis[J].Infect Dis,2005,191 (12):2138-2148.
    [81]Vall Westerloo DJ, Giebelen IA, Florquin S, et al. The vagus nerve and nicotinic receptors modulate experimental pancreatitis severity in mice[J]. Gastroenterology,2006,130(6): 1822-1830.
    [82]Van Maanen MA, Vervoordeldonk MJ, Tak PP. The cholinergic anti-inflammatory pathway: towards innovative treatment of rheumatoid arthritis[J]. Nat Rev Rheumatol,2009,5(4): 229-232.
    [83]Li T, Zuo X, Zhou Y et al. The vagus nerve and nicotinic receptors involve inhibition of HMGB 1 release and early pro-inflammatory cytokines function in collagen-induced arthritis[J]. Journal of clinical immunology,2010,30(2):213-220.
    [84]The FO, Boeckxstaens GE, Snoek SA, et al. Activation of the cholinergic anti-inflammatory pathway ameliorates postoperative ileus in mice[J]. Gastroenterology,2007,133(4): 1219-1228.
    [85]De Jonge WJ, Van der Zanden EP, The FO,et al. Stimulation of the vagus nerve attenuates macrophage activation by activating the Jak2-STAT3 signaling pathway[J]. Nat Immunol. 2005,6(8):844-851.
    [86]Van Maanen MA, Lebre MC, van der Poll T, et al. Stimulation of nicotinic acetylcholine receptors attenuates collagen-induced arthritis in mice[J]. Arthritis Rheum,2009,60(1): 114-122.
    [87]Li T, Zuo X, Zhou Y et al. The vagus nerve and nicotinic receptors involve inhibition of HMGB 1 release and early pro-inflammatory cytokines function in collagen-induced arthritis[J]. Journal of clinical immunology,2010,30(2):213-220.
    [88]Waldburger JM, Boyle DL, Pavlov VA, et al. Acetylcholine regulation of synoviocyte cytokine expression by the alpha7 nicotinic receptor[J]. Arthritis Rheum,2008,58(11): 3439-3449.
    [89]Wang H, Liao H, Ochani M, et al. Cholinergic agonists inhibit HMGB 1 release and improve survival in experimental sepsis[J]. Nat Med,2004,10(11):1216-1221.
    [90]Lindblad SS, Mydel P, Jonsson IM, et al. Smoking and nicotine exposure delay development of collagen-induced arthritis in mice[J]. Arthritis Res Ther,2009,11(3):R88.
    [91]Van Maanen MA, Vervoordeldonk MJ, Tak PP. The cholinergic anti-inflammatory pathway: towards innovative treatment of rheumatoid arthritis[J]. Nat Rev Rheumatol,2009,5(4): 229-232.
    [92]Li T, Zuo X, Zhou Y et al. The vagus nerve and nicotinic receptors involve inhibition of HMGB 1 release and early pro-inflammatory cytokines function in collagen-induced arthritis[J]. Journal of clinical immunology,2010,30(2):213-220.
    [93]周金黄主编.抗炎药物筛选规程药理学进展[M].北京:人民卫生出版社,1982,176.
    [94]金问祯,等.鼠类胸膜炎模型与抗炎抗风湿药物研究[J].中国药理学通报,1986,2(2):42.
    [95]吕爱平.类风湿关节炎中西医结合应用基础研究[M].北京:中医古籍出版社,1999.23-32.
    [96]Zhang Jinyu, Rheumatoid Arthritis[M]. Beijing:People's Medical Publishing House, 1998,524-526.
    [97]左亚杰,等.疏风通络片抗炎镇痛作用的实验研究[J].河北中医药学报,2002,17(1):25-27.
    [98]Easser RE, Hildebr and AR,AngeloRA, et al. Measurement of radiographic changes in adjuvantinduced arthritis in rats by quantitative image analysis[J]. Arthritis Rheum,1995, 38:129.
    [99]马东来.等.大鼠佐剂性关节炎的诱导及其免疫异常研究[J].中国实验临床免疫学杂志,1995,7(3):13-17.
    [100]Lewis AJ, et al. Pharmacology of inflammation[J]. Amsterdam:Elsevier S cience Puli, 1985:376-378.
    [101]Roberts BV, In:Dick WC, et al. Recent advance in rheumatology. Vol 3.New York:Pitman, 1983:73-98
    [102]卫生部科教司.医学实验动物模型及红细胞学研制与应用[M].1984:168.
    [103]黄迪君,等.灸刺法对实验性RA大鼠血液流变学的影响[J].中国针灸,1996,41-43.
    [104]馗文海,石奉文,张惠民,等.关节腔内注射尿素治疗实验性类风湿性关节炎[J].中国康复医学杂志,1994,9(1):24-26.
    [105]陈奇主编.中药药理实验方法学[M].北京:人民卫生出版社,1994,68.
    [106]章鸣,高根德.羟甲基几丁糖的兔佐剂性关节炎滑膜细胞体外培养影响的试验研究[J]浙江临床医学,2002,4(6):405-406.
    [107]Hughel E Buttery L, Hukkanen M, et al. Gytokine induced PGE synthesis and cox-2 activity ale regulated both by anitric oxide dependent and independent mechanism in rat osteoblasts in vitro [J]. Biol Chem,1999,274(3):1776-1782.
    [108]Ulloa, L. The vagus nerve and the nicotinic anti-inflammatory pathway[J]. Nat ReV Drug Discov,2005,4(8):673-684.
    [109]Van Maanen MA, Lebre MC, van der Poll T, et al. Stimulation of nicotinic acetylcholine receptors attenuates collagen-induced arthritis in mice[J]. Arthritis Rheum,2009,60(1): 114-122.
    [110]Lindblad SS, Mydel P, Jonsson IM, et al. Smoking and nicotine exposure delay development of collagen-induced arthritis in mice[J]. Arthritis Res Ther,2009,11(3):R88.
    [111]蒋明等.风湿病学[M].科学出版社,124.
    [112]Bromley M, et al. Histopathology of teh rheumatoid lesion:identificatoin of cell types at sites of acrtilage erosion[J]. Arthritis Rhirm,1984,27:857.
    [113]Edwards, J.C.W, et al. Membrane properties and esterase activity of synovial lining cells, evidence for a mononuclear phagocyte population[J]. Ann. Rheum. Dis,1982,41:282.
    [114]Zvaifler NJ, et al. Pannus and pannocytes. Alternative models of joint destruction in rheumatoid arthritis[J]. Arthritis Rheum,1994,37:783.
    [115]Kinne R W, et al. expression of jun-B and c-fos proto-oncogenes by activated fibroblast-like cells in synovial tissue of rheumatoid arthritis and osteoarthritis patients[J]. Arthritis Rheum,1993,36:264.
    [116]Muller-Ladner U, et al. Activation of synoviocytes. Curr Opin Rheumabol[J].2000,12:186.
    [117]Raimund W Kinne, et al. Activation of synovial fibroblast in rheumatoid arthritis[J]. Annals of the Rheumatic Diseases.1995,54:501.
    [118]Trabandt A, et al. Expression of the collagenolytic and ras-induced cysteine proteinase cathepsin L and proliferation-associated oncogenes in synovial cells of MRL/1 mice and patients with rheumatoid arthritis[J]. Matrix,.1990.10:349.
    [119]杨慎峭,刘旭光,余曙光,等.艾灸对类风湿性关节炎家兔关节滑膜液IL-1β、TNF含量的影响[J].成都中医药大学学报,2005,28(3):11-12.
    [120]刘旭光,杨慎峭,余曙光,等.艾灸对实验性类风湿性关节炎家兔关节滑膜液MMP-3、 TIMP-1含量的影响[J].成都中医药大学学报,2005,28(4):1-2.
    [121]Wang H, Liao H,Ochani M, et al. Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis[J]. Nature Med.2004,10(11):1216-1221.
    [122]张强华.类风性湿关节炎的发病机制[J].国外医学免疫学分册,1994,(1):40-43.
    [123]Nakajima H,et al. the effect of treatment with interferon gamma on type II collagen induced arthritis. Clin Exp Immunol 1990,81:441
    [124]徐春晓.肿瘤坏死因子受体生物学功能及其临床应用研究进展[J].微生物学免疫学进展,2003,3l(1):37.
    [125]蔡青,等.类风湿关节炎的病理生理及生物学治疗进展[J].中华风湿病学杂志,2000,4(3):183-286.
    [126]Firestein GS.Invasive fibroblase-like synoviocytes in rheumatoid arthritis passive responders or transformed aggressor? [J]. Arthritis Rheum.1996.39:1781-1790.
    [127]Isomaki P, et al. The presence of inter-leukin-13 in rheumatoid synovium and its anti-inflammatory effects on synovial fluid macrophages from Patients with rheumatoid arthritis[J]. Arthritis Rheum,1996,39:1693-1702.
    [128]Deleuran BW, et al. Localization of tumor necrosis factor receptor in the synovial tissues and cartilage-pannus junction in patients with rheumatoid arthritis:implications for local actions of tumor necrosis factor-a[J]. Arthritis Rheum,1992,35:1170-1178.
    [129]仁洁,齐义成.类风湿性关节炎与细胞凋亡[J].天津医药,2004,32(4):255.
    [130]Grom AA, et al. Patterns of expression of tumor necrosis factor α, tumor necrosis factor β, and their receptors in synovial of patients with juvenile spondy larthropathy[J]. Arthritis Rheum,1996,39:1703-1710.
    [131]Arend WP, et al. Cytokine and inhibitors or antagonists in rheumatoid arthritis[J]. Arthritis Rheum,1990,33:305-310.
    [132]Mistune H, Yudoh K, Katakana R, et al. The role of TNF-alpha in the pathogenesis of inflammation and joint destruction in rheumatoid arthritis(RA):a study using ahumanRA/ SCID mouse chimera[J]. Rheumatology(Oxford),2002,41(3):329-337.
    [133]William RA, Dayer JM. Cytokines and cytokine inhibitors or antagonists in rheumatoid arthritis[J]. Arthritis Rheum,1990,33(3):305-315.
    [134]David ML, Miehael EW. Rheumatoid Arthritis[J]. Lancet,2001,358(9285):903-911.
    [135]Dayer JM. The pivotal role of interleukin- in the clinical manifestations of Rheumatoid arthritis[J]. Rheumatology,2003,42(suppl2):3-10.
    [136]VuolteenahoK, Moilane T, Hamalainen M, et al. Regulation of nitric oxide production in osteoarthritis and rheumatoid cartilage, Role of endogenous IL-1 inhibitors. Scand[J]. Rheumatology,2003,32(1):19-24.
    [137]Roams E, Gillespie MT, Martin TJ. Indecent of receptor activator of NF-Kappa B ligand and tumor necrosis factor alpha in bone destruction[J]. Bone,2002,30(2):340-346.
    [138]Tyler J A. Articular cartilage cultured with catabilin (pig IL-1) Syntheses a decreased number of normal proteoglycan molecules[J]. Biochem,1985,227.869-878.
    [139]Yin T. Involvement of IL-6 signal transducergp 130 in IL-1 1- mediated signal transduction[J]. Immunol,1993,151:2555-2561.
    [140]Volin, M.V, Huynh, N., Klosowska, K., et al. Fractalkine is a novel chemoattractant for rheumatoid arthritis fibroblast-like synoviocyte signaling through MAP kinases and Akt[J]. Arthritis Rheum,2007,56(8):2512-2522.
    [141]Rose-John S. lnterleukin-6 biology is coordinated by membrane bound and soluble receptors[J]. Acta Biochim P01,2003,50(3):603-611.
    [142]Carter SD, Barnes A. Gilmore WH[J]. Vetimmunol Immunopathol,1999,69(2-4):201-214.
    [143]Feldmann M, Maini RN. [J]. Rheumatology oxford,1999,38(Supple2):3-7.
    [144]Klimiuk PA, Sierakowski S, Chwiecko J. Serum interleukin 6(IL-6) concentration correlates with matrix metalloproteinase and their tissue inhibitors in rheumatoid arthritis[J]. Pol Arch Med Wewn,2003,109(2):119-123.
    [145]Goodwin GH, Sander C, Johns EW. A new group of chromatin-associated proteins with a high content of acidic and basic amino acids[J]. Eur J Biochem,1973,38(3):14-19.
    [146]Yamada S, Maruyama. HMGB1, a novel inflammatory cytokine[J]. Clin Chim Acta,2007, 375(1-2):36-42.
    [147]Gardella S, Andrei C, Ferrera D et al.The nuclear protein HMGB1 is secreted by monocytes via a non classical,vesicle mediated secretory pathway[J]. EMBO Rep,2002,3(10): 995-1001.
    [148]Yang H, Wang H, Christopher J, et al. The cytokine activity of HMGB1[J]. Journal of Leukocyte Biology,2005,78(1):1-8.
    [149]Chen G, Ward MF, Sama AE,, et al. Extracellular HMGB1 as a proinflammatory cytokine[J]. Interferon Cytokine Res,2004,24(6):329-333.
    [150]Tang D, Shi Y, Jang L, et al. Heat shock response inhibits release of high mobility group boxl protein induced by endotoxin in murine macrophages[J].Shock,2005,23(5):434-440.
    [151]Fiuza C, Bustin M. Inflammation-promoting activity of HMGB1 on human microvascular endothelialcells[J]. Blood,2003,101(7):2652-2660.
    [152]Pisetsky DS, Erlandsson-Harris H, Andersson U. High mobility group box protein 1 (HMGB1):an alarmin mediating the pathogenesis of rheumatic disease[J]. Arthritis ResTher,2008,10(3):209.
    [153]Andcrsson, J. The inflammatory reflex-introduction[J]. Intern Med,2005,257(2):122-125.
    [154]Taniguchi N, Kawahara K, Yone K, et al. High mobility group box chromosomal protein 1 plays a role in the pathogenesis of rheumatoid arthritis as a novel cytokine[J]. Arthritis Rheumatism,2003,48(4):971-981.
    [155]Andersson U, Erlandsson-Harris H. HMGB1 is a potent trigger of arthritis[J]. J Intern Med 2004,255(3):344-350.
    [156]Taniguchi N, Kawahara K, Yone K, et al. High mobility group box chromosomal protein 1 plays a role in the pathogenesis of rheumatoid arthritis as a novel cytokine[J]. Arthritis Rheumatism,2003,48(4):971-981.
    [157]Kokkola R, Sundberg E, Ulfgren AK et al. High mobility group box chromosomal protein 1: a novel proinflammator mediator in synovitis[J]. Arthritis Rheum,2002,46(10):2598-2603.
    [158]Pullerits R, Jonsson IM, Verdrengh M. High mobility group box chromosomal protein 1, a DNA binding cytokine, Induces Arthritis[J]. Arthritis Rheum,2003,48(6):1693-1700.
    [159]Li T, Zuo X,Zhou Y et al. The vagus nerve and nicotinic receptors involve inhibition of HMGB 1 release and early pro-inflammatory cytokines function in collagen-induced arthritis[J].Journal of clinical immunology,2010,30(2):213-220.
    [160]Kokkola R, Li J, Sundberg E et al. Successful treatment of collagen-induced arthritis in mice and rats by targeting extracellular high mobility group box chromosomal protein 1 activity [J]. Arthritis Rheum,2003,48(7):2052-2058.
    [161]Borovikova LV, Ivanova S, Zhang MH, et al. Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin [J]. Nature,2000,405(6785):458-462.
    [162]Tracey KJ, Czura CJ. Janova S. Mind over immunity[J]. FASEB J,2001,15:1575-1576.
    [163]Czura Cj, Friedman SG, Tracey KJ. Neural Inhibition of inflammation:the cholinergic anti-inflammatory pathway[J]. Endotoxin Res,2003,9(6):409-413.
    [164]Kawashima K, Fujii T. The lymphocytic cholinergic system and its contribution to the regulation of immune activity[J]. Life Sci,2003,74(6):675-696.
    [165]Arenault AL, Lhotak S, Hunter WL, et al. Taxol involution of collagen-induced arthritis: ultrastructural correlation with the inhibition of synovitis and neovascularization[J]. Clin Immunol Immunopathol,1998,86:280-289.
    [166]Kawashima K, Fujii T. Expression of non-neuronal acetylcholine in lymphocytes and its contribution to the regulation of immune function[J]. Front Biosci,2004,9:2063-85.
    [167]周亚欧.胆碱能抗炎通路在类风湿关节炎中的作用及机制研究[D].长沙:中南大学,2008,58-62.
    [168]The FO, Boeckxstaens GE, Snoek SA, et al. Activation of the cholinergic anti-inflammatory pathway ameliorates postoperative ileus in mice[J]. Gastroenterology,2007,133(4): 1219-1228.
    [169]Hamano R, Takahashi HK, Iwagaki H, et al. Stimulation of alpha7 nicotinic acetylcholine receptor inhibits CD 14 and the toll-like receptor 4 expression in human monocytes[J]. Shock,2006,26(4):358-364.
    [170]De Jonge WJ, Ulloa L. The alpha7 nicotinic acetylcholine receptor as a pharmacological target for inflammation[J]. Br J Phamacol,2007,151(7):915-929.
    [171]王金荣,王宏伟,刘胜洪,等.大鼠免疫细胞及器官的固有胆碱能系统[J].中华神经医学杂志,2005,4(1),28-31.
    [172]Poggetti RS, Moore FA, Moore Ee, et al. Liver injury is a reversible neutrophil-mediated event following gut ischemia[J]. Arch Surg,1992,127(2):175-179.
    [173]Hogg RC, Raggenbass M, Bertrand D, et al. Nicotinic acetylcholine receptors, from structure to brain function[J]. Physiol Biochem Pharmacol,2003,147:1-46.
    [174]Sato E, koyama S, Okubo, Y, et al. Axetylcholine stimulates alveolar macrophage to release inflammatory cell chemotacticactivity[J]. Am Physiol,1998,274:979-979.
    [175]Wang H, Yu M, Ochani M, et al. Nicotinic acetylcholine receptor alpha7 subunit is an essential regulator of inflammation[J]. Nature,2003,421(6921):384-388.
    [176]Bernik TR, Friedman SG, Ochani M, et al. Pharmacological stimulation of the cholinergic anti-inflammatory pathway[J]. Experimental Medicine,2002,195:781-788.
    [177]de Jonge, W.J., van der Zanden, E.P., The, F.O., et al. Stimulation of the vagus nerve attenuates macrophage activation by activating the Jak2-STAT3 signaling pathway[J]. Nat Immunol,2005,6(8):844-851.
    [178]Borovikova LV, Ivanova S, Zhang MH, et al. Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin [J]. Nature,2000,405(6785):458-462.
    [179]杨藻宸.药理学和药物治疗学[M].第1版.北京:人民卫生出版社,2000,357-359.
    [180]Gil-Bea FJ, Garcia Alloza M, Dominguesz J, et al. Evaluation of cholinergic markers in Alzheimer's disease and in a model of cholinergic deficit [J]. Neurosci Lett,2005, 375(1):37-41.
    [181]Markowska AL, Olton DS. Cholinnergic manipulations in the medial septal area:age-related effects on working memory and hippocampal electrophysiology [J]. The Journal of Neuroseience,1995,15(3):2063-2073.
    [182]朱长庚.神经解剖学[M].北京:人民卫生出版社,2002,716-718.
    [183]Oda Y. Choline acetyltransferase:the structure, distribution and pathologic changes in the central nervous system[J]. Pathol lnt,1999,49(11):921-937.
    [184]李小鹰.心血管疾病分子生物学[M].北京:人民军医出版社,2000:220.
    [185]Ahn K S, Sethi G, Aggarwal B B. Nuclear factor-kappa B:from clone to clinic[J]. Curt MolMed,2007,7(7):619-637.
    [186]Hayden MS, Ghosh S. Shared principles in NF-κB signaling [J]. Cell,2008,132(3): 344-362.
    [187]Chen FE, and Ghosh G. Regulation of DNA binding by Rel/NF-k B transcription factots structural [J]. Oncogene,1999,18(49):6845-6852.
    [188]May MJ, Ghosh S. Sianal transduction through NF-κB [J]. Immunology Today,1998, 19:80-88.
    [189]Barnes PJ, Karin M. Nuclear factor kappa B:a pivotal transcription factor in Chronic inflammatory diseases [J]. New English Med,1997,336(15):1066-1071.
    [190]Gomez PF, Pillinger MH, Atteur M, et al. Resolution of inflammation:prostagland in E2 dissociates nuclear trafficking of individual NF-κB subunits(p65,p50) in stimulated rheumatoid synovial fibroblasts [J]. J Immunol,2005,175(10):6924-6930.
    [191]Aya K, Ahawagri M. Hagen-Stapleton A, et al. NF-κB inducing kinase controls lymphocyte and osteoclast activities in inflammatory arthritis[J].J Clin Invest.2005,115(7):1848-1854.
    [192]Sergei S, Makam~ SS. NF-KB in rheumatoid arthritis:a pivotal-lator of inflammation, hyperplasia and tissue destruction [J]. Arthritis Res,2001,3:200-206.
    [193]Sergei S Makarov. NF-κB in rheumatoid arthritis:a pivotal regulator of inflammation,hyperplasia and tissue destruction [J]. Arthritis Res,2001,3:200-206.
    [194]AUPPERLE K R, BENNE'IT B L, HAN z, et al. NF-KB Regulation by hoB Kinase-2 in Rheumatoid Arthritis Synoviocytes[J]. J Immunol,2001,166:2705-2711.
    [195]H Asahara,M Asanuma, N Ogawa, S Nishibayashi, H Inoue. High DNA-binding activity of transcripfion factor NF-kappa B in synovial membranes of pafients with rheumatoid arthritis [J]. Biochem Mol Biol hat,1995,37:827-832.
    [196]PW Tsao, T Suzuki, R Totsaka;et al. The effect ofdexamethasoue 0/1 the expression of activated NF-kappa B in adjuvant arthritis [J]. Clin immunol innmmopathol,1997,83: 173-178.
    [197]VJ Palombella, EM Conner, JW Fuseler, et al. Role of the proteasome and NF-kappaB in s treptococcal cell wallqnduced polyarthritis [J]. Proe Natl.&cad Sei USA,1998,95: 15671-15676.
    [198]Z Han, DL Boyle, AM Manning, GS Firestein. AP-1 and NF-kappa B regalation inrheumatoid thritis and murine collagen-induced arthritis [J]. Autoimmanity,1998,28: 197-208.
    [199]Tak PP, Firestein GS. NF-kappaB:a key role in inflammatory diseases[J]. J Clin Invest, 2001,107(1):7-11.
    [200]Tsao PW, Suzuki T, Totsuka R, et al. The efect of dexamethasone on the expression of activated NF-Kappa B in adjuvant arthritis [J]. Clin Immunol Immunopathol,1997,83(2): 173-178.
    [201]Bond M, Chase AJ, Baker AH, et al. Inhibition of transcription factor NF-kappaB reduces m8tI'lX metalloproteinase:1,-3 and-9 production by vascular smooth muscle ceils [J]. Cardiovasc Res,2001,50(3):556-565.
    [202]M Bond, AH Baker, AC Newby. Nuclear factor kappa B activity is essential for matrixmetalloproteinase-1 and o upregulation in rabbit dermal flbroblasts [J]. Biochern Biophys Res Commun,1999,264:561-567.
    [203]Benito MJ, Murphy E, Murphy EP, et al. Increased synovial tissue NF-Kappa BI expression at sites adjacent to the cartilage-pannus junction in rheumatoid arthritis[J]. Arthritis Rheum, 2004,50(6):1781-1787.
    [204]John C,Bhabesh C.Direct inhibition of NF-κB blocks bone erosion associated thinflammatory arthritis [J].J Immunol,2003,171:5547-5553.
    [205]孙天英,赵凤,等.血管内皮生长因子和核因素-κB在CIA大鼠滑膜组织中的表达[J].华北煤炭医学院学报,2009,11(1):5-6.
    [206]Gomez PF, Pillinger MH, Attur M, et al. Resolution of inflammation:prostaglandin E2 dissociates nuclear trafficking of individual NF-kappaB subunits (p65, p50) in stimulated rheumatoid synovial fibroblasts [J]. J Immunol.,2005,175(10):6924-6930.
    [207]Baldwin Jr AS. The NF-κB and IκB proteins:new discoveries and insights [J]. Annu Rev mmunol,1996.,14(1):649-681.
    [208]Ghosh G. NF-kappaB and Rel proteins:evolutionary conserved mediators of the nlune response [J]. Annu Rev Innmaunol,1998,16:225.
    [209]Zhong H, May MJimi E, el al. The phosphorylation status of nucler NF-kappa B determinesits association with CBP/p300 or HDAC-1 [J]. Mol Cell,2002,9:625-636.
    [210]Beg A A, Sha W C, Bronson R T.el al. Embryonic lethality and liver degeneration in micelacking the RelA eomponant of NF-kappa B [J]. Nature,1995,167-169.
    [211]Whiteside ST, Israel A. I kappa B proteins:structure, function and regulation [J]. Semin Cancer Bin,1997,8(2):75-82.
    [212]Whiteside ST, Israel A. I kappa B proteins:structure, function and regulation [J]. Semin Cancer Bin,1997,8(2):75-82.
    [213]Ghosh S, Karin M. Missing pieces in the NF-kappaB puzzle [J]. Cell,2002,109:S81-S96.
    [214]Hoffmann A, Levchenko A, Scott L M,et al. The IkappaB-NF-kappa B signaling module: temporal control and selective gene activation[J]. Science,2002,298(5595) 1241-1245.
    [215]Hayden MS. Ghosh S. Signaling to NF-kappa B[J]. Genes Dev.2004,18(18):2195-2224.
    [216]赵文树,杨智荣,姜超,等.溃结灵Ⅲ号治疗肝郁脾虚型溃疡性结肠炎31例[J].中医药信息,2005,22(3):47-49.
    [217]Zandi E, Karin M. Bridging the gap:composition, regulation and physiological function of the I kappa B kinase complex[J]. Mol Cell Bio,1999,19:4547-4551.
    [218]Yang F, tang E, Guan K, et al. IKK beta plays an essential role in the phosphorylation of RelA/p65 on serine 536 induced by lipopolysaccharide [J]. Immunol,2003,170(11): 5630-5635.
    [219]Zandi E, Karin M. Bridging the gap:composition, regulation and physiological function of the I kappa B kinase complex[J]. Mol Cell Bio,1999,19:4547-4551.
    [220]Aupperle KR Bennett BE, Manning AM, Boyle DI. Firestein GS. I kappa B kinase (IKK2), but not IKK1, is the convergent pathway for cytokine-induced NF-kappa B Signaling in fibroblast-like synovioeytes[J]. J Immunol,2001,166:2705-2711.
    [221]Aupperle K, Bennett B, Han z, et al. NF-Kappa Bregulation by I Kappa B kinase-2 in rheumatoid arthritis synoviacytes[J]. J Immunol,2001,166(4):2705-2711.
    [222]Tak PP, Gedag DM, Auppefle KR, et al. Inhibitor of nuclear factorkappa B kinase beta is a key regulator Of synovial inflammation [J]. Arthritis Rheum,2001,44(8):1897-1907.
    [1]Ulloa, L. The vagus nerve and the nicotinic anti-inflammatory pathway[J]. Nat ReV Drug Discov,2005,4(8):673-684.
    [2]Tracey KJ. The inflammatory reflex[J]. Nature,2002,420:853-859.
    [3]Tracey K J. Physiology and immunology of the cholinergic anti-inflammatory pathway[J]. JClin Invest,2007,117(2):289-296.
    [4]Borovikova LV, Ivanova S, Zhang MH, et al. Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin[J]. Nature,2000,405(6785): 458-462.
    [5]Hong Wang, ManYu,Mahendar Ochani, et al. Nicotinic acetylcholine receptor a7 subunit is an essential regulator of inflammation[J]. Nature,2003, 421(6921):384-388.
    [6]WANG Bo-jie, SU Yue. Development of research on cholinergic anti-inflammatory Pathway[J]. In J Anesth Resus,2006,27(4),242-245.
    [7]Czura CJ, Friedman SG, Tracey KJ. Neural inhibition of inflammation:the cholinergic anti-inflammatory pathway[J]. J Endotoxin Res,2003,9(6):409-413.
    [8]Rosas-Ballina M, Tracey K J. Cholinergic control of inflammation [J]. Journal of Internal Medicine,2009,265:663.
    [9]Wang H, Liao H, Ochani M et al. Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis[J]. Nat Med,2004,10(11):1216-1221.
    [10]Wang H, Yu M, Ochani M, et al.Nicotinic acetyrIcholine receptor alpha7 subunit is an essential regulator of inflammation[J]. Nature,2003,421(6921):384-388.
    [11]Villiger Y, Szantol, Jaconi S, et al. Expression of an alpha7 duplicate nicotinic acetylcholine receptor-related protein in human leukocytes [J]. Neuroimmunol, 2002,126(1-2):86-98.
    [12]李琪,刘霞.胆碱能抗炎通路的信号机制研究[J].药学实践杂志,2010,28(5):325-327.
    [13]DeJonge WJ, VanderZanden EP, TheFO et al. Stimulation of the vagus nerve attenuates macrophage activation by activating the Jak2-STAT3 signaling pathway [J]. Nat Immunol,2005,6(8):844-851.
    [14]胡森.兴奋胆碱能抗炎通路干预炎症与缺血引起的器官损害[J].感染、炎症、修复,2008,9(4):195.
    [15]Liu JH, Yan J, Hu JM, et al. Effects of electroacupuncture on gastric myoeletric activity and substance P in the dorsal vagal comples of rats[J]. Neuroscience Letters,2004,356(2):99-102.
    [16]刘健华,李江山,严洁,等.针刺“足三里”对大鼠孤束核P物质的影响[J].针刺研究,2003,28(1):5.
    [17]王景杰,黄裕新.c-fos在电针调控大鼠胃运动中的表达及其意义[J].针刺研宄,2001,26(4):274-278.
    [18]胡森,宋琪,王磊,等.电针兴奋胆碱能抗炎通路减轻内毒素引起的细胞因子释放和脏器功能损害[J].中国中西医结合急救杂志,2008,15(4):205-208.
    [19]李建国,彭周全,杜朝晖,等.电针足三里激活胆碱能抗炎通路抗大鼠失血性休克的研究[J].中国中西医结合急救杂志,2006,13(1):29-33.
    [20]张立德,柴纪严.针刺对健康家兔体表胃电图和17肽胃泌素的影响[J].中 国针灸,1996,1:27-30.
    [21]Ouyang H, Yin JS, Chen JD, et al. Electroacupuncture accelerates gastric emptying in association with changes in vagal activityp[J]. American Physiological Socipty,2002,282,390-396.
    [22]王景杰,黄裕新.心理性应急壮态下针刺对大鼠DMV放电、胃电和胃黏膜损伤的影响[J].第四军医大学学报,2001,22(9):806-809.
    [23]王景杰,黄裕新.C-fos在电针调控大鼠胃运动中的表达及其意义[J].针刺研宄,2001,26(4):274-278.
    [24]曹艳,刘伟华,张万峰.“关元穴”烧山火刺法对家兔失血性休克、血压、温度的影响[J].中医药信息,1999,2:62-62.
    [25]Ouyang H, Yin JY, Wang ZS, et al. Electroacupuncture accelerates gastric emptying in association with changes in vagal activity[J]. Am J Physiol Gastrointest Liver Physiol,2002,282(2):390-396.
    [26]张立德等.针刺对健康家兔体表胃电图和17肽胃泌素的影响[J].中国针灸,1996,26(1):27-30.
    [27]Liu JH, Yan J, Hu JM, et al. Effeets of electroacupuncture on gastric myoeletric activity and substance P in the dorsal vagal eomples of rats[J]. Neurosei Lett, 2004,356(2):99-102.
    [28]Chou JW, Chang YH, Chang CS, et al. The effect of different frequency electrical acu-stimulation on gastric myoelectrical activity in healthy subjects[J]. Hepatogastroenterology,2003,50(50):582-586.
    [29]Ouyang H, Yin JY, Wang ZS, et al. Electroacupuncture accelerates gastric emptying in association with changes in vagal activity[J]. Am J Physiol Gastrointest Liver Physiol,2002,282(2):390-396.
    [30]吴红金,周雷,薛峥,等.电针抗大鼠急性炎症性内脏痛的肠神经机制[J].针刺研究,1999,24(2):138.
    [31]张立德,冯起国,王德山,等.电针足三里对重症肌无力(MG)大鼠神经-肌肉接头传递的影响[J].中国针灸,1998,25:92-95.
    [32]张立俭,黄振俊,白慧颖,等.电针足三里干预大鼠腹腔粘连的实验研究[J].中医学报,2011,26(12):1466-1468.
    [33]田易军,王磊,耿世佳,等.电针足三里减轻大鼠术后腹腔粘连的实验研究[J].感染、炎症、修复,2005,9(3):153-156.
    [34]胡森,宋琪,王海滨,等.电针足三里对内毒素所致大鼠肝损伤保护机制的研究[J].中国中西医结合急救杂志,2007,14(5):296-298.
    [35]胡森,张立俭,白慧颖,等.电针足三里对脓毒症大鼠促炎症因子所致肝损伤的保护作用[J].医学研究杂志,2009,38(10):25-28.
    [36]李叶晟,徐峰,李洪海,等.电针刺激大鼠足三里穴对肝缺血再灌注损伤的保护作用[J].第二军医大学学报,2011,32(2):191-194.
    [37]胥阳,宋学敏,李建国,等.电针足三里对严重烫伤大鼠凝血功能和血浆促炎性细胞因子的影响[J].武汉大学学报,2012,33(4):453-456.
    [38]胡森,王磊,周国勇,等.针刺足三里穴减轻烫伤大鼠肠缺血引起的氧自由基损伤[J].西北国防医学杂志,2010,31(1):1-3.
    [39]袁翔,李建国,黄越,等.电针足三里激活胆碱能抗炎通道抗大鼠感染性休克[J].武汉大学学报(医学版),2007,28(2):203-206.
    [40]胡森,王磊,周洁平.电针足三里对烫伤休克大鼠肠黏膜血流和微血管通透性的影响[J].微循环学杂志,2010,20(1):10-12.
    [41]李建国,彭周全,杜朝晖,等.电针足三里激活胆碱能抗炎通路抗大鼠失血性休克的研究[J].中国中西医结合急救杂志,2006,13(1):27-31.
    [42]张立俭,石现,白慧颖,等.电针足三里对脓毒症大鼠促炎症因子所致心肌损伤的保护作用[J].军医进修学院学报,2010,31(4):377-381.
    [43]胡森,宋琪,石德光,等.兴奋胆碱能抗炎通路对内毒素致心肌损害的保护作用[J].感染、炎症、修复,2008,9(3):134.
    [44]胡森,张立俭,白慧颖,等.电针足三里对脓毒症大鼠组织肿瘤坏死因子和多脏器功能损害的影响[J].中国病理生理杂志,2010,26(2):353-356.
    [45]胡森,张立俭,白慧颖,等.电针足三里对脓毒症大鼠小肠促炎症因子、二胺氧化酶活性及组织含水率的影响[J].世界华人消化杂志,2009,17(20):2079-2082.
    [46]赵玉雪,何伟,高听妍,等.电针耳甲区对内毒素血症模型大鼠的抗炎保护作用[J].针刺研究,2011,36(3):187-192.

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