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作 者:韦登明[1] 王一凡[1] 王琳[1] 龙正海[2]
机构地区:[1]宁波大学医学院,浙江宁波315211 [2]浙江医药高等专科学校,浙江宁波315100
出 处:《中华中医药学刊》2009年第11期2413-2416,共4页Chinese Archives of Traditional Chinese Medicine
基 金:宁波市科技局社会发展攻关项目(2006C100059)
摘 要:目的:探讨雷公藤内酯醇对佐剂性关节炎大鼠病变关节组织MIP-1α、RANTES和VEGF表达的影响。方法:在建立大鼠佐剂性关节炎模型基础上,给予不同剂量雷公藤内酯醇后,观察病变关节组织病理损害程度和MIP-1α、RANTES和VEGF免疫组织化学染色结果。结果:与模型组比较,3个雷公藤内酯醇治疗组关节肿胀度和病变关节组织MIP-1α、RANTES和VEGF表达明显减少,病变关节组织的病理损害明显改善。结论:雷公藤内酯醇可抑制佐剂性关节炎大鼠病变关节组织MIP-1α、RANTES和VEGF表达。Objective: To study the inhibitory effects of Triptolide (TL) on expression of MIP -1α, RANTES and VEGF in adjuvant - induced arthritis rats. Methods : Rat arthritis model waz induced by adjuvant, TL was given at does of 0. 1- 0.4mg/kg, The MIP-1α, RANTES and VEGF protein expression in arthritis tissue was examined by immunohisto- chemistry ,The macroscopical and histological changes of the arthrite were checked. Results: Compared with model group, the expression of MIP -1α, RANTES and VEGF were remarkably reduced, the macroscopical and histological changes were significantly improved in TL - treated rats ( P 〈 0.05,P 〈 0.01 ). Conclusion: triptolide can inhibite production of MIP -1α, RANTES and VEGF in arthrits tissue of adjuvant induced rats.
关 键 词:雷公藤内酯醇 佐剂性关节炎 MIP-1α:[{ANTES VEGF
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