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海克苷在完全弗氏佐剂诱导的关节炎大鼠中通过抑制促炎细胞因子发挥抗关节炎活性。

Hecogenin exhibits anti-arthritic activity in rats through suppression of pro-inflammatory cytokines in Complete Freund's adjuvant-induced arthritis.

机构信息

a Institute of Pharmacy , Nirma University , Ahmedabad , Gujarat , India.

b Sinhgad Institute of Pharmaceutical Sciences , Pune , Maharashtra , India.

出版信息

Immunopharmacol Immunotoxicol. 2018 Feb;40(1):59-71. doi: 10.1080/08923973.2017.1405439. Epub 2017 Dec 1.

Abstract

Hecogenin is a steroidal sapogenin isolated from the leaves of Agave genus species that plays an important role in the treatment of a variety of inflammatory diseases. The aim of the present study was to evaluate the anti-arthritic activity of hecogenin in Complete Freund's adjuvant-induced arthritis in rats. The hecogenin (40 µl of 50 µg/kg, orally) and hecogenin + fluticasone (40 µl of 25 µg/kg, each, orally) was tested against Complete Freund's adjuvant-induced arthritis in rats by evaluating various parameters such as paw volume, arthritic score, joint diameter, spleen weight, thymus weight, haematological and biochemical parameters and pro-inflammatory cytokines. Histopathological and radiological analyzes of ankle joints were also carried out. Treatment of rats with hecogenin and its combination elicited significant reduction in paw edema, arthritic score and joint diameter. Hecogenin and its combination also inhibited joint destruction in histopathological and radiological analyzes of ankle joint. Hecogenin and its combination significantly increased the levels of red blood cells and hemoglobin but decreased the white blood cell count. The anti-arthritic activity was also confirmed with the change in biochemical parameters and myeloperoxidase assay. In the present investigation, hecogenin and its combination prevent destruction of cartilage and protect synovial membrane with improving health status through haematonic properties and down regulation of various cytokines. Hence, hecogenin may be a potential therapeutic candidate for the treatment of rheumatoid arthritis.

摘要

荆芥醇是一种从龙舌兰属植物叶子中分离出来的甾体皂素,在治疗多种炎症性疾病中发挥着重要作用。本研究旨在评估荆芥醇在完全弗氏佐剂诱导的大鼠关节炎中的抗关节炎活性。荆芥醇(50μg/kg,40μl,口服)和荆芥醇+氟替卡松(25μg/kg,40μl,口服)用于评估爪体积、关节炎评分、关节直径、脾脏重量、胸腺重量、血液学和生化学参数以及促炎细胞因子等各种参数,以评估其对完全弗氏佐剂诱导的关节炎大鼠的影响。还对踝关节进行了组织病理学和放射学分析。荆芥醇及其组合治疗可显著减少爪水肿、关节炎评分和关节直径。荆芥醇及其组合还抑制了组织病理学和放射学分析中踝关节的关节破坏。荆芥醇及其组合还显著增加了红细胞和血红蛋白水平,但降低了白细胞计数。通过改变生化参数和髓过氧化物酶测定,也证实了其抗关节炎活性。在本研究中,荆芥醇及其组合通过血液学特性和下调各种细胞因子来预防软骨破坏和保护滑膜,从而改善健康状况,可能成为治疗类风湿关节炎的潜在治疗候选物。

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