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祛风息痛丸对大鼠佐剂性关节炎的治疗作用 被引量:13

Therapeutic effect of Qufeng Xitong Wan on adjuvant arthritis in rats
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摘要 目的观察祛风息痛丸对佐剂性关节炎的治疗作用,为其临床治疗类风湿性关节炎提供实验依据。方法建立佐剂性关节炎大鼠模型,采用玻璃容器法测定大鼠原发性和继发性足爪肿胀度。采用酶联免疫吸附试验测定血清白细胞介素1(IL-1)和肿瘤坏死因子α(TNFα)含量。结果祛风息痛丸0.26,0.78和2.34g.kg-1连续灌胃3d显著抑制佐剂性关节炎大鼠原发性足爪肿胀,对致炎后18h的肿胀抑制率分别为21.4%,36.8%和65.0%。同剂量祛风息痛丸连续灌胃30d对佐剂性关节炎大鼠继发性即非致炎侧关节肿胀具有明显的抑制作用,并可明显降低多发性关节炎病变评分,中、大剂量可明显降低血清IL-1和TNFα含量。结论祛风息痛丸对实验性佐剂性关节炎具有治疗作用。 AIM To investigate the therapeutic effect of Qufeng Xitong Wan (QFXTW) on rheumatoid arthritis. METHODS The rat model of adjuvant arthritis (AA) was established. The primary and secondary swelling extent in hind paws was detected by using volume testing method and the serum levels of interleukin-1 (IL-1) and tumor necrosis factor-α (TNFct) were measured with enzyme-linked immunosorbent assay. RESULTS In AA rats, QFXTW 0. 26,0. 78 and 2. 34 g·kg^-1 (ig) for 3 d obviously inhibited the right paw swelling, the primary inflammation, and the swelling inhibition rates were 21.4%, 36.8% and 65.0%, respectively. QFXTW at the same doses (ig) for 30 d suppressed the left paw swelling, the secondary inflammation, and reduced the scores of polyarticular arthritis markedly. QFXTW 0.78 and 2.34 g·kg^-1 also decreased the serum levels of IL-1 and TNFα. CONCLUSION QFXTW has therapeutic effect on experimental AA in rats.
出处 《中国药理学与毒理学杂志》 CAS CSCD 北大核心 2007年第5期422-426,共5页 Chinese Journal of Pharmacology and Toxicology
关键词 祛风息痛丸 治疗应用 关节炎 实验性 Qufeng Xitong Wan therapeutic use arthritis, experimental
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  • 1Xu SY, Bian RL, Chen X. Methodology of Pharmacological Experiments(药理实验方法学) [M] //3rd ed. Beijing: People's Medical Publishing House, 2002:915.
  • 2Chen Q. Methodology of Pharmacological Experiments of Chinese Medicine(中药药理实验方法学) [M]//Beijing: People's Medical Publishing House, 1993:369-371.
  • 3张国恩,杨德华,钱玉中,胡冬菊,姚筱梅.痹康饮合剂对佐剂性关节炎大鼠的实验研究[J].北京中医药大学学报,2006,29(2):104-107. 被引量:16
  • 4Abbott JD, Moreland LW. Rheumatoid arthritis: developing pharmacological therapies[J]. Expert Opin Investig Drugs, 2004, 13(8) :1007 -1018.
  • 5Badolato R, Oppenheim JJ. Role of cytokines, acute - phase proteins, and chemokines in the progression of rheumatoid arthritis [J]. Semin Arthritis Rheum, 1996, 26(2) :526 -538.
  • 6Cai X, Wong YF, Zhou H, Liu ZQ, Xie Y, Jiang ZH, et al. Manipulation of the induction of adjuvant arthritis in Sprague-Dawley rats [J]. Inflamm Res, 2006, 55 (9) :368 - 377.
  • 7Abramson SB, Amin A. Blocking the effects of IL-1 in rheumatoid arthritis protects bone and cartilage [J]. Rheumatology (Oxford), 2002, 41(9):972-980.
  • 8Marshall N J, Wilson G, Lapworth K, Kay LJ. Patients' perceptions of treatment with anti-TNF therapy for rheumatoid arthritis : a qualitative study [J]. Rheumatology, 2004, 43:1034 - 1038.
  • 9Cai X, Zhou H, Wong YF, Xie Y, Liu ZQ, Jiang ZH, et al. Suppression of the onset and progression of collagen-induced arthritis in rats by QFGJS, a preparation from an anti-arthritic Chinese herbal formula[J]. J Ethnopharmacol, 2007, 110(1) :39-48.
  • 10Pearson CM. Experimental models in rheumatoid disease [J]. Arthritis Rheum, 1964, 7:80 -86.

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