类风湿关节炎脾虚病证结合大鼠模型的建立

Du Zhongping , Zhao Hongyan , Xiao Cheng , Liu Meijie , Wang Yan , Lv Cheng , Lv Aiping , Wang Shaojun , Teng Jingru , Ju Dahong
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引用次数: 2

摘要

本研究旨在建立脾虚型类风湿关节炎(RA)病证结合大鼠模型。将60只6周龄SpragueDawley大鼠随机分为正常对照组和利血平(RSP)组。采用RSP腹腔注射造脾虚模型大鼠组。14 d后,RSP组大鼠皮下注射II型胶原蛋白诱导关节炎。观察模型发生率,并采用酶联免疫吸附试验(ELISA)分析其作用机制。结果显示,与胶原诱导关节炎(CIA)组相比,RSP CIA模型关节肿胀程度和关节损伤程度明显增加。RSP CIA模型大鼠表现出与临床症状相似的脾虚证,表现为无精打采、眯眼、被毛稀疏干燥暗沉、驼背、踝关节肿胀、乏力、运动懒散、不聚、少食、体重减轻、便稀。与CIA对照大鼠相比,脾虚使肠绒毛紊乱,上皮内大量杯状细胞被覆盖,形成脱落、变性、坏死绒毛块,使肠黏膜功能受损。抗II型胶原抗体、IL-6、IL-10、IFN-γ含量升高。由此可见,利血平腹腔注射类风湿性关节炎脾虚证大鼠模型既具有明显的脾虚证,又具有类风湿关节炎的特点。为类风湿关节炎脾虚证大鼠模型的建立提供了成功的经验。脾虚在类风湿关节炎中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establishment of Disease-syndrome Combination Rat Model of Rheumatoid Arthritis with Spleen Deficiency

This study was aimed at establishing a disease-syndrome combination rat model of rheumatoid arthritis (RA) with spleen deficiency. A group of 60 six-week-old SpragueDawley rats were randomly divided into normal control group and reserpine (RSP) group. Spleen deficiency model rat groups were made by an intraperitoneal injection of RSP. After 14 days, rats of RSP groups were subcutaneously injected with collagen type II protein to induce arthritis. The incidence of the model was observed, and the mechanism was analyzed by enzyme-linked immunosorbent assay (ELISA). The results showed that compared with the collagen-induced arthritis (CIA) group, the degree of joint swelling and joint damage was significantly increased in the RSP CIA model. The RSP CIA model rats were observed as exhibiting spleen deficiency syndrome that was similar to clinical symptoms, such as appearing apathetic, squinting, a sparse dry dull coat, a bowed back, a swollen ankle, fatigue, lazy movement, getting together, eating less, weight loss, and loose stools. Compared with the CIA control rats, spleen deficiency impaired the function of intestinal mucosa by disordering the intestinal villi, covering a large amount of goblet cells in the epithelium, and inducing exfoliation, degeneration, and necrosis fluff pieces. The content of anti-type II collagen antibody, IL-6, IL-10, and IFN-γ was increased. It was concluded that the rat model of rheumatoid arthritis with spleen deficiency syndrome by an intraperitoneal injection of reserpine has both obvious spleen deficiency syndrome and characteristics of RA. It can provide successful experiences for the rat model of rheumatoid arthritis with spleen deficiency syndrome. Spleen deficiency plays a vital role in RA.

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