Evaluation of the anti-inflammatory activity of Tinospora cordifolia (Willd.) Miers chloroform extract - a preclinical study

被引:28
|
作者
Philip, Sheena [1 ,2 ]
Tom, Greeshma [1 ,2 ]
Vasumathi, Asha V. [1 ]
机构
[1] Rajiv Gandhi Ctr Biotechnol, Plant Based Bioact & Dis Biol Lab, Thiruvananthapuram 695014, Kerala, India
[2] Univ Kerala, Thiruvananthapuram, Kerala, India
关键词
drugs from natural sources; Tinospora cordifolia; anti-inflammatory; COX-2; FACTOR-KAPPA-B; NITRIC-OXIDE; MEDICINAL-PLANTS; INFLAMMATION; CANCER; CYCLOOXYGENASE-2; CELLS; EXPRESSION; PATHWAYS; ROLES;
D O I
10.1111/jphp.12932
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
ObjectivesTinospora cordifolia (Willd.) Miers is an inevitable ingredient of Ayurvedic rasayanas for the treatment of disorders with unregulated inflammation. However, studies regarding the mechanism of anti-inflammatory potential of this plant at the molecular level are lacking. MethodsIn vitro evaluations were conducted in RAW264.7 macrophages which were preincubated with chloroform extract of T.cordifolia (CETC) and subsequently stimulated with LPS. The expressions of COX-2, TNF- and iNOS genes were analysed by SQRT-PCR and Western blot, cytokines (IL-6, IL-1 and PGE(2)) levels by ELISA, NF-B activation and p38 MAPK phosphorylation by Immunoblot and confocal imaging. Anti-inflammatory potential of CETC was validated further in a rat model of carrageenan-induced hind paw edema. Phytochemical characterisation was carried out using the HPLC technique. Key findingsThe LPS-induced upregulation of proinflammatory biomarkers was significantly prevented by CETC, without inhibiting COX-1. CETC- and LPS-incubated cells showed reduced phosphorylated p38 MAPK levels, and higher levels NF-B were retained in cytoplasm. Rats pretreated with CETC showed a statistically significant decrease in paw oedema (P0.05), and HPLC characterisation detected stigmasterol and -sitosterol. The LD50 of CETC lies above 2000mg/Kg body weight. ConclusionsThese findings encourage us strongly to focus on CETC to develop anti-inflammatory drugs with lower degree of inhibition to the constitutively expressing COX-1.
引用
收藏
页码:1113 / 1125
页数:13
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