Rat/mono-arthritis model |
6.2 mg/kg |
oral |
Reduction of edema swelling volume, lymphocyte and monocyte infiltration |
Mouse/TPA-induced skin model |
1 and 2.5 µmol |
topical application |
Reduction of iNOS and COX-2 |
Rat PCA model |
1 and 5 mg/kg |
oral |
Reduction of DNP-HAS-induced PCA by 72% and 45% |
Mouse/ischemic acute kidney injury model |
20 mg/kg |
i.p. |
Involvement of NFκB and HO-1reduction of creatinine, blood urea nitrogen and mRNA of neutrophil gelatinase-associated lipocalin, neutrophil infiltration, andIL-6, MCP-1, MIP-2, and KC mRNA |
Hamster, buccal pouch carcinogenesis model |
20 mg/kg |
oral |
Reduction of DMBA-induced IKK, p65, COX, and iNOS levelsBlock of IκBα degradation and IL-6,IL-1 and TNFReduction of NFκB and AP-1 mRNA expression and c-jun, c-fos protein levels |
Mouse, middle cerebral artery occlusion-induced brain damage model |
5 and 20 mg/kg |
oral |
Reduction of brain infarct volume, MDA and ROS production, IL-1β, TNF, COX-2 and iNOS, ERK, JNK, and p38 activation |