首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Protective Effects of Simvastatin and Hesperidin against Complete Freund's Adjuvant-Induced Rheumatoid Arthritis in Rats
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Protective Effects of Simvastatin and Hesperidin against Complete Freund's Adjuvant-Induced Rheumatoid Arthritis in Rats

机译:辛伐他汀和橙皮苷对完全弗氏佐剂诱导的类风湿关节炎的保护作用

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Background/Aims: Rheumatoid arthritis (RA) is a disabling autoimmune disease for which most current treatments cause massive complications, thereby limiting treatment dose and duration. The anti-arthritic effects of the 3-hydroxy-3-metylglutary-CoA reductase inhibitor, simvastatin, and the natural flavonoid, hesperidin, were investigated against complete Freund's adjuvant-induced RA in rats. Methods:A normal control group, an arthritis control group, 2 reference treatment groups receiving dexamethasone (1.5 mg/kg/day) and methotrexate (1 mg/kg/day), and 2 treatment groups receiving simvastatin (0.5 mg/kg/day) and hesperidin (200 mg/kg/day) were included in the study. Serum rheumatoid factor, matrix metalloprotinease-3 (MMP-3) and cartilage oligomeric matrix protein (COMP) as specific rheumatoid biomarkers, serum immunoglobulin G (IgG) and antinuclear antibody (ANA) as immunological biomarkers, serum tumor necrosis factor-alpha and interleukin-10 as immunomodulatory cytokines, serum myeloperoxidase (MPO) and C-reactive protein as inflammatory biomarkers, and malondialdehyde (MDA) and glutathione (GSH) as oxidative stress biomarkers were assessed, supported by joint and spleen histopathological study. Results: Simvastatin significantly improved all the measured biomarkers, with MMP-3, COMP, and GSH restored to normal levels. Hesperidin significantly improved all the measured biomarkers, with COMP, IgG, ANA, MPO, MDA and GSH restored to normal levels. Conclusion: Simvastatin and hesperidin may be promising protective agents against RA through immunomodulatory, anti-inflammatory and antioxidant potentials. (C) 2015 S. Karger AG, Basel
机译:背景/目的:类风湿关节炎(RA)是一种致残性自身免疫疾病,目前大多数治疗方法都会引起严重的并发症,从而限制了治疗剂量和持续时间。研究了3-羟基-3-甲基谷氨酸-CoA还原酶抑制剂辛伐他汀和天然类黄酮橙皮苷对大鼠完全弗氏佐剂诱导的RA的抗关节炎作用。方法:正常对照组,关节炎对照组,2个接受地塞米松(1.5 mg / kg /天)和甲氨蝶呤(1 mg / kg /天)的参考治疗组,以及2个接受辛伐他汀(0.5 mg / kg /天)的治疗组)和橙皮苷(200 mg / kg /天)也包括在研究中。血清类风湿因子,基质金属蛋白酶3(MMP-3)和软骨寡聚基质蛋白(COMP)作为类风湿生物标志物,血清免疫球蛋白G(IgG)和抗核抗体(ANA)作为免疫生物标志物,血清肿瘤坏死因子-α和白介素在关节和脾组织病理学研究的支持下,对-10作为免疫调节细胞因子,血清髓过氧化物酶(MPO)和C反应蛋白作为炎症生物标志物,丙二醛(MDA)和谷胱甘肽(GSH)作为氧化应激生物标志物进行了评估。结果:辛伐他汀可显着改善所有测得的生物标志物,MMP-3,COMP和GSH恢复至正常水平。橙皮苷显着改善了所有测得的生物标志物,COMP,IgG,ANA,MPO,MDA和GSH恢复至正常水平。结论:辛伐他汀和橙皮苷可能通过免疫调节,抗炎和抗氧化作用成为有希望的抵抗RA的保护剂。 (C)2015 S.Karger AG,巴塞尔

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