期刊文献+

穿山龙总皂苷对CIA大鼠滑膜血管新生的作用 被引量:18

EFFECTS OF TOTAL SAPONIN OF RHIZOMA DIOSCREAE NIPPONICAE ON ANGIOGENESIS IN SYNOVIAL MEMBRANE OF CIA RATS
下载PDF
导出
摘要 目的:探讨穿山龙总皂苷对胶原诱导性关节炎(collagen-induced arthritis,CIA)大鼠滑膜血管新生及血管内皮生长因子(vascular endothelial growth factor,VEGF)表达的作用。方法:42只Wistar大鼠随机分为7组:正常对照组(A组)、CIA模型组(B组)、雷公藤组(C组)、穿山龙总皂苷高剂量组(D组)、穿山龙总皂苷中剂量组(E组)、穿山龙总皂苷低剂量组(F组)和薯蓣皂苷元组(G组),每组6只大鼠。B-G组大鼠均建立CIA大鼠模型,待模型成功建立后,C-G组大鼠分别给予相应的药物灌胃,连续21d。采用免疫组织化学染色法检测关节滑膜的微血管密度(MVD)和VEGF的表达。结果:CIA模型组大鼠滑膜MVD和VEGF的表达显著高于正常对照组(P<0.01;)C-G组大鼠滑膜MVD和VEGF的表达明显低于模型组(P<0.01),且各治疗组间比较无显著差异(P>0.05)。结论:穿山龙总皂苷可能通过降低关节滑膜VEGF的表达发挥抑制滑膜血管新生的作用。 Objective:To investigate effects of total saponin of Rhizoma Dioscreae Nipponicae (RDN) on angiogenesis and expression of vascular endothelial growth factor (VEGF) in synovial membrane of collageninduccd arthritis (C1A) rats.Methods:42 Wistar rats were randomly divided into 7 groups (n=6): normal control group (A), CIA model group (B), Tripterygium group (C), RDN high dose group (D), RDN middle dose group (E), RDN low dose group (F) and Diosgenin group (G). Rats in B-G group were established CIA rat model; then the rats in C-G group were lavaged with corresponding medicine for 21 days. Immunohistochemical staining was used to detect MVD and VEGF expression in synovial membrane.Results:MVD and VEGF expression in synovial membrane of CIA rats were obviously higher than normal control rats (P〈 0.01); MVD and VEGF expression in synovial membrane of rats in each treatment group were obviously lower than CIA model rats (P〈 0.01); moreover, there had no obvious differences between each treatment group (-P〉 0.05). Conclnsions:RDN can inhibit angiogenesis in synovial membrane by down regulating VEGF expression.
机构地区 承德医学院
出处 《承德医学院学报》 2010年第4期360-362,共3页 Journal of Chengde Medical University
基金 国家自然基金项目(30873420) 河北省自然基金重点项目(C2007000916)
关键词 CIA 穿LIJ龙总皂苷 血管新生 血管内皮生长因子 CIA Total saponin ofRhizoma Dioscreae Nipponicae Angiogenesis VEGF
  • 相关文献

参考文献7

二级参考文献35

  • 1马东来,李俊.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. 被引量:60
  • 2Eriksson K, Magnusson P, Dixelius J, et al. Angiostatin and endostatin inhibit endothelial cell migration in response to FGF and VEGF without interfering with specific intracellular signal transduction pathways[J ]. FEBS Letters, 2003, 536 (1-3): 19.
  • 3Klimiuk P A, Sierrakow S, Latosiewicz R, et al. Serum matrix matelloproteinases and tissue inhibitor of matelloproteinases in differenthistological variants of rheumatoid synovitis[J]. Rheumatology (Oxford), 2002, 41(1): 78.
  • 4Litinsky I, Paran D, Levartovsky D, et al. The effects of leflunomide on clinical parameters and serum levels of IL-6, IL-10, MMP-1 and MMP-3 in patients with resistant rheumatoid arthritis[J]. Cytokine, 2006, 33(2): 106.
  • 5Cunnane G, Fitzgerald O, Beeton C, et al. Early joint erosions and serum levels of matrix metalloproteinase 1, matrix metalloproteinase 3, and tissue inhibitor of metalloproteinases 1 in rheumatoid arthritis[J]. Arthritis Rheum, 2001, 44 (10) : 2263.
  • 6Arroyo A G, Genis L, Gonzalo P, et al. Matrix metalloproteinases: new mutes to the use of MT1-MMP as a therapeutic target in angiogenesis-related disease[J]. Curr Pharm Des, 2007, 13(17): 1787.
  • 7Koenders M I, Joosten L A, van den Berg W B. Potential new targets in arthritis therapy: interleukin (IL)-17 and its relation to tumour necrosis factor and IL-1 in experimental arthritis[J]. Ann Rheum Dis, 2006, 65(supp13) : iii29.
  • 8Latour F, Zabraniecki L, Dromer C, et al. Does vascular endothelial growth factor in the rheumatoid synovium predict joint destruction? A clinical, radiological, and pathological study in 12 patients monitored for 10 years[J]. Joint Bone Spine, 2001, 68(6): 493.
  • 9Bijman M N, van Nieuw Amerongen G P, Laurens N, et al, Microtubule-targeting agents inhibit angiogenesis at subtoxic concentrations, a process associated with inhibition of Rac1 and Cdc42 activity and changes in the endothelial cytoskeleton [J]. Mol Cancer Ther, 2006, 5(9): 2348.
  • 10Sottile J. Regulation of angiogenesis by extracellular matrix [J]. Biochim Biophys Acta, 2004, 1654(1): 13.

共引文献306

同被引文献234

引证文献18

二级引证文献154

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部