Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/9915
Title: Hecogenin Exhibits Anti-Arthritic Activity in Rats Through Suppression of Pro-Inflammatory Cytokines in Complete Freund’s Adjuvant-Induced Arthritis
Authors: Ingawale, Deepa K.
Patel, Snehal S.
Keywords: Rheumatoid Arthritis
Complete Freund’s adjuvant
Hecogenin
Fluticasone
Proinflammatory cytokines
Myeloperoxidase
Issue Date: 2017
Publisher: Taylor & Francis
Series/Report no.: IPFP0371;
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 ml of 50 mg/kg, orally) and hecogeninþ fluticasone (40 ml of 25 mg/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, haem atological and biochemical parameters and pro-inflammatory cytokines. Histopathological and radio logical 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
Description: Immunopharmacology and Immunotoxicology; 40(1), 1-13: 2017
URI: http://10.1.7.192:80/jspui/handle/123456789/9915
Appears in Collections:Faculty Papers

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