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Inhibitory effect of Coptis chinensis on inflammation in LPS-induced endotoxemia.

AbstractETHNOPHARMACOLOGICAL RELEVANCE:
Rhizoma coptidis (RC) has been used as a remedy for inflammation-related diseases in traditional medicine. Although it is known to have anti-inflammatory activities, its mechanism of action on lipopolysaccharide (LPS)-induced inflammation has not yet been identified in detail.
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.
AuthorsYou Yeon Choi, Mi Hye Kim, Ik-Hyun Cho, Ji Hee Kim, Jongki Hong, Tae Hee Lee, Woong Mo Yang
JournalJournal of ethnopharmacology (J Ethnopharmacol) Vol. 149 Issue 2 Pg. 506-12 (Sep 16 2013) ISSN: 1872-7573 [Electronic] Ireland
PMID23871807 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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
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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