Guo Yachun, Xing Enhong, Liang Xiujun, Song Hongru, Dong Wenjuan
Department of Pathogen Biology, Chengde Medical College, Hebei, China.
Central Laboratory, the Affiliated Hospital of Chengde Medical College, Hebei, China.
J Chin Med Assoc. 2016 May;79(5):264-71. doi: 10.1016/j.jcma.2015.10.012.
This study aimed to determine the effects of total saponins from Rhizoma Dioscoreae Nipponicae (TS-RDN) on the expression of vascular endothelial growth factor (VEGF) and angiopoietin (Ang)-2 and Tie-2 (endothelial tyrosine kinase receptor) receptors in the synovium of rats with rheumatoid arthritis (RA) (collagen-induced arthritis; CIA), and to examine the mechanisms of TS-RDN in alleviating RA.
The CIA rat model was established and the animals were randomly divided into control, CIA model, TS-RDN, diosgenin, and tripterygium groups. Fluorescent polymerase chain reaction was performed to detect VEGF expression in the rat knee joint synovium. Additionally, immunohistochemical assay was used to detect protein expression of Ang-2 and Tie-2 in the rat knee joint synovium.
Expression of VEGF, Ang-2, and Tie-2 in the model group was significantly higher than in the control group (p < 0.01). After TS-RDN, tripterygium and diosgenin treatment, VEGF and Ang-2 expression was lower than in the model group (p < 0.01). However, Tie-2 expression showed no significant difference. The effects of TS-RDN on VEGF expression were more marked than those of tripterygium and diosgenin (p < 0.01).
TS-RDN might reduce the expression of VEGF, Ang-2, and Tie-2 in the synovium, thus inhibiting synovial angiogenesis and playing a therapeutic role in RA.
本研究旨在确定穿龙薯蓣总皂苷(TS-RDN)对类风湿关节炎(RA)(胶原诱导性关节炎;CIA)大鼠滑膜中血管内皮生长因子(VEGF)、血管生成素(Ang)-2及Tie-2(内皮酪氨酸激酶受体)受体表达的影响,并探讨TS-RDN缓解RA的机制。
建立CIA大鼠模型,将动物随机分为对照组、CIA模型组、TS-RDN组、薯蓣皂苷元组和雷公藤多苷组。采用荧光聚合酶链反应检测大鼠膝关节滑膜中VEGF的表达。此外,采用免疫组织化学法检测大鼠膝关节滑膜中Ang-2和Tie-2的蛋白表达。
模型组VEGF、Ang-2和Tie-2的表达显著高于对照组(p < 0.01)。TS-RDN、雷公藤多苷和薯蓣皂苷元治疗后,VEGF和Ang-2的表达低于模型组(p < 0.01)。然而,Tie-2的表达无显著差异。TS-RDN对VEGF表达的影响比雷公藤多苷和薯蓣皂苷元更显著(p < 0.01)。
TS-RDN可能降低滑膜中VEGF、Ang-2和Tie-2的表达,从而抑制滑膜血管生成并在RA中发挥治疗作用。