Abstract | AIM OF THIS STUDY:
GCSB-5 is a traditional medicine preparation composed with six oriental herbs which have been widely used for the inflammatory diseases in Asia. In the present study, we have demonstrated the anti-inflammatory effects of GCSB-5 in vivo and in vitro along with its underlying mechanism of action. METHODS: The acute and chronic inflammation models in animals were applied to investigate the anti-inflammatory effects of GCSB-5. To further investigate the mechanism of the anti-inflammatory activity, lipopolysaccharide (LPS)-induced murine macrophage RAW264.7 cells were also employed. RESULTS: CONCLUSIONS: Taken together, our results demonstrate that GCSB-5 reduces the development of acute and chronic inflammation and its anti-inflammatory property might in part be a function of the inhibition of iNOS and COX-2 expression via down-regulation of the Akt signal pathway and inhibition of NF-kappaB activation. These findings suggest that GCSB-5 might be an applicable therapeutic traditional medicine in the regulation of the inflammatory response.
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Authors | Hwa-Jin Chung, Hak-Sun Lee, Joon-Shik Shin, Sang-Ho Lee, Byung-Mo Park, You-Suk Youn, Sang Kook Lee |
Journal | Journal of ethnopharmacology
(J Ethnopharmacol)
Vol. 130
Issue 3
Pg. 450-9
(Aug 09 2010)
ISSN: 1872-7573 [Electronic] Ireland |
PMID | 20621661
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2010 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- Anti-Inflammatory Agents
- NF-kappa B
- Plant Extracts
- Nitric Oxide Synthase Type II
- Cyclooxygenase 2
- Proto-Oncogene Proteins c-akt
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Topics |
- Acute Disease
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Cell Line
- Chronic Disease
- Cyclooxygenase 2
(drug effects, genetics)
- Disease Models, Animal
- Inflammation
(drug therapy, physiopathology)
- Macrophages
(drug effects, metabolism)
- Male
- Medicine, East Asian Traditional
- Mice
- Mice, Inbred ICR
- NF-kappa B
(antagonists & inhibitors)
- Nitric Oxide Synthase Type II
(drug effects, genetics)
- Phytotherapy
(methods)
- Plant Extracts
(pharmacology)
- Proto-Oncogene Proteins c-akt
(drug effects, metabolism)
- Rats
- Rats, Sprague-Dawley
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