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首页> 外文期刊>Pharmaceuticals >Oral Administration of Shark Type II Collagen Suppresses Complete Freund’s Adjuvant-Induced Rheumatoid Arthritis in Rats
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Oral Administration of Shark Type II Collagen Suppresses Complete Freund’s Adjuvant-Induced Rheumatoid Arthritis in Rats

机译:鲨鱼II型胶原的口服给药可抑制大鼠完全弗氏佐剂诱导的类风湿关节炎

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Objective: Shark type II collagen (SCII) is extracted as a glycoprotein from the cartilage of blue shark (Prionace glauca). We aim to confirm the effects of oral tolerance of SCII on inflammatory and immune responses to the ankle joint of rheumatoid-arthritis rats induced by Complete Freund’s Adjuvant (CFA). Materials and Methods: The onset of rheumatoid arthritis (RA) was observed 14 ± x days after injection of CFA. Rats in the control group were treated with acetic acid by oral administration (0.05 mmol kg−1d−1, days 14–28), while rats in experimental groups were treated by oral administration with SCII (1 or 3 mg kg−1d−1, days 14–28), Tripterygium wilfordii polyglycosidium (TWP) (10 mg kg−1d−1, days 14–28), and bovine type II collagen from US (US-CII) (1 mg kg−1d−1, days 14–28), respectively. The severity of arthritis was evaluated by the articular swelling. The immunological indexes observed included delayed type hypersensitivity (DTH) reaction, the level of interleukins 10 (IL-10) in rat blood serum and morphological characterization. Mixed lymphocyte culture (MLC) was performed to investigate the relationship between T cell apoptosis and specific immune tolerance induced by SCII. Results: Treatment with SCII for 2 weeks significantly attenuated the acute inflammation. The rats orally administrated with SCII at the level of 3 mg kg−1d−1 (SCII 3) and US-CII had decreased DTH reaction compared with rats in control group. Rats treated with SCII 3 had the highest level of IL-10 with 102 pg/mL. SCII with concentration of 10 μg/L could help to significantly enhance level of Fas/Apo-1 in T cell in vitro. The result of histological staining indicated that the recovery of the articular membranes of ankle joint in SCII 3 group was greatly enhanced. Conclusions: Our results suggest that appropriate dose of SCII can not only ameliorate symptoms but also modify the disease process of Complete-Freunds-Adjuvant-induced arthritis. Oral administration of SCII might be a potential candidate as a novel drug for further investigation.
机译:目的:从蓝鲨(Prionace glauca)的软骨中提取糖蛋白II型鲨鱼(SCII)作为一种糖蛋白。我们旨在确认SCII的口服耐受性对完全弗氏佐剂(CFA)诱导的类风湿关节炎大鼠踝关节的炎症和免疫反应的影响。材料和方法:注射CFA后14±x天观察到类风湿关节炎(RA)的发作。对照组大鼠口服醋酸治疗(0.05mmol kg -1 d -1 -1,第14-28天),而实验组大鼠通过口服SCII(1或3 mg kg −1 d -1 ,第14-28天),雷公藤多苷(TWP)(10 mg kg -1 d -1 ,第14-28天),以及来自美国的II型牛胶原蛋白(US-CII)(1 mg kg -1 d < sup> -1 ,分别是14-28天)。通过关节肿胀评估关节炎的严重程度。观察到的免疫学指标包括迟发型超敏反应(DTH),大鼠血清中白介素10(IL-10)的水平和形态学特征。进行混合淋巴细胞培养(MLC)以研究T细胞凋亡与SCII诱导的特异性免疫耐受之间的关系。结果:SCII治疗2周可显着减轻急性炎症。与对照组相比,口服SCII 3 mg kg -1 d -1 (SCII 3)和US-CII的大鼠DTH反应降低。用SCII 3治疗的大鼠的IL-10水平最高,为102 pg / mL。浓度为10μg/ L的SCII可能有助于显着提高体外T细胞中Fas / Apo-1的水平。组织学染色结果显示,SCII 3组踝关节的关节膜恢复明显增强。结论:我们的结果表明,适当剂量的SCII不仅可以缓解症状,而且可以改善完全弗氏佐剂引起的关节炎的发病过程。口服SCII可能作为新药有待进一步研究。

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