Abstract | ETHNOPHARMACOLOGICAL RELEVANCE: AIM OF THE STUDY: This study was designed to assess the beneficial effects of pretreatment with RC in ameliorating LPS-induced liver inflammation. MATERIALS AND METHODS: Mice were orally administered RC (500, 1000 mg/kg) for three days in a row. 1h after the last RC administration, the mice were intraperitoneally injected with LPS (35 mg/kg). After treatment, histological alterations and inflammatory factor levels in the liver and proinflammatory cytokines in the serum associated with inflammation were examined. RESULTS: We found that pretreatment with RC (500 and 1000 mg/kg) exerted a significant protective effect by attenuating liver histopathological changes in endotoxemic mice. The results also demonstrated that RC suppressed secretion of LPS-stimulated pro-inflammatory cytokines, such as interleukin-6 (IL-6). Furthermore, RC inhibited LPS-mediated nuclear factor (NF)-κB activation via the prevention of IκB-α phosphorylation, as well as the phosphorylation of ERK1/2, JNK, and p38 MAPKs. These results were associated with decreases in the expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (I-NOS). CONCLUSIONS: The results presented here clearly demonstrate that RC could significantly protect mice against LPS-induced acute liver injury.
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Authors | You Yeon Choi, Mi Hye Kim, Ik-Hyun Cho, Ji Hee Kim, Jongki Hong, Tae Hee Lee, Woong Mo Yang |
Journal | Journal of ethnopharmacology
(J Ethnopharmacol)
Vol. 149
Issue 2
Pg. 506-12
(Sep 16 2013)
ISSN: 1872-7573 [Electronic] Ireland |
PMID | 23871807
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2013 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- Anti-Inflammatory Agents
- I-kappa B Proteins
- Interleukin-6
- Lipopolysaccharides
- NF-kappa B
- Nfkbia protein, mouse
- NF-KappaB Inhibitor alpha
- Interferon-gamma
- Nitric Oxide Synthase Type II
- Nos2 protein, mouse
- Ptgs2 protein, mouse
- Cyclooxygenase 2
- Mitogen-Activated Protein Kinases
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Topics |
- Animals
- Anti-Inflammatory Agents
(pharmacology, therapeutic use)
- Coptis
- Cyclooxygenase 2
(metabolism)
- Endotoxemia
(chemically induced, drug therapy, metabolism, pathology)
- Female
- Hepatitis
(drug therapy, metabolism, pathology)
- I-kappa B Proteins
(metabolism)
- Interferon-gamma
(blood)
- Interleukin-6
(blood)
- Lipopolysaccharides
- Liver
(drug effects, metabolism, pathology)
- Mice
- Mice, Inbred ICR
- Mitogen-Activated Protein Kinases
(metabolism)
- NF-KappaB Inhibitor alpha
- NF-kappa B
(metabolism)
- Nitric Oxide Synthase Type II
(metabolism)
- Rhizome
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