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      Antipyretic and anti-inflammatory effects of asiaticoside in lipopolysaccharide-treated rat through up-regulation of heme oxygenase-1.

      Phytotherapy Research
      Animals, Anti-Inflammatory Agents, pharmacology, Antipyretics, Centella, chemistry, Cyclooxygenase 2, genetics, metabolism, Dinoprostone, Heme Oxygenase (Decyclizing), Inflammation, drug therapy, Interleukin-10, blood, Interleukin-6, Lipopolysaccharides, Liver, enzymology, Male, Peroxidase, Rats, Rats, Sprague-Dawley, Triterpenes, Tumor Necrosis Factor-alpha, Up-Regulation, drug effects

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          Abstract

          Asiaticoside (AS), a triterpenoid isolated from Centella asiatica, has been found to exhibit antioxidant and anti-inflammatory activities in several experimental animal models. However, the underlying mechanisms remain elusive. In this study, we provide experimental evidences that AS dose-dependently inhibited lipopolysaccharide (LPS)-induced fever and inflammatory response, including serum tumor necrosis factor (TNF)-α and interleukin (IL)-6 production, liver myeloperoxidase (MPO) activity, brain cyclooxygenase-2 (COX-2) protein expression and prostaglandin E2 (PGE2 ) production. Interestingly, AS increased serum IL-10 level, liver heme oxygenase-1 (HO-1) protein expression and activity. Furthermore, we found that the suppressive effects of AS on LPS-induced fever and inflammation were reversed by pretreatment with ZnPPIX, a HO-1 activity inhibitor. In summary, our results suggest that AS has the antipyretic and anti-inflammatory effects in LPS-treated rat. These effects could be associated with the inhibition of pro-inflammatory mediators, including TNF-α and IL-6 levels, COX-2 expression and PGE2 production, as well as MPO activity, which might be mediated by the up-regulation of HO-1. Copyright © 2012 John Wiley & Sons, Ltd.

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