Therapeutic effects of gentiopicroside on adjuvant-induced arthritis by inhibiting inflammation and oxidative stress in rats

被引:30
|
作者
Xie, Xiaoqian [1 ]
Li, He [1 ,2 ]
Wang, Yale [1 ]
Wan, Zhijie [1 ]
Luo, Shasha [1 ]
Zhao, Zeyue [1 ]
Liu, Jingjing [1 ]
Wu, Xiaohan [1 ]
Li, Xinxin [1 ]
Li, Xiaotian [1 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, 100 Kexue, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Pharm, Zhengzhou 450001, Henan, Peoples R China
关键词
Rheumatoid arthritis; Gentiopicroside; Antioxidant; Anti-inflammation; NF-KAPPA-B; RHEUMATOID-ARTHRITIS; CARDIOVASCULAR-DISEASE; SYNOVIAL INFLAMMATION; ANIMAL-MODELS; ACTIVATION; CYTOKINES; OSTEOCLASTOGENESIS; METHOTREXATE; PATHWAYS;
D O I
10.1016/j.intimp.2019.105840
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The purpose of this research was to evaluate the therapeutic effects of gentiopicroside (GPS) on adjuvant-induced arthritis (AA) rats. Rats were injected with complete Freund's adjuvant (CFA) for 0.1 mL in the right hind paw to induce AA. Thirty rats from three groups were treated with GPS (30, 60, 90 mg/kg) from day 15 to day 26. Arthritis was evaluated by arthritis index, paw volume, paw thickness, and X-ray. The effect of GPS on inflammation was assessed by measuring the levels of interleukin (IL)-1 beta, tumor necrosis factor (TNF)-alpha, IL-6 and IL-17, as well as related mRNA. Glutathione peroxidase (GSH-Px), superoxide dismutase (SOD), glutathione (GSH) protein carbonyl (PCO) and malondialdehyde (MDA) were measured to assess the effect of GPS on oxidative stress. These results indicate that GPS increases the levels of GSH-Px, SOD and GSH, and reduces the levels of MDA and PCO. GPS can significantly down-regulate the levels of IL-1 beta, TNF-alpha, IL-6 and IL-17, as well as related mRNA. In addition, X-ray and histopathological results show that GPS has a therapeutic effect on joints in AA rats. In summary, the therapeutic effects of GPS on AA rats are associated with anti-inflammation and antioxidation.
引用
收藏
页数:9
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