Armillariella mellea shows anti-inflammatory activity by inhibiting the expression of NO, iNOS, COX-2 and cytokines in THP-1 cells.

Abstract

Armillariella mellea (AM), also known as Mi-Huan-Ku, a popular medicinal fungus used in the traditional Chinese medicine for treating headache, neurasthenia and insomnia. In the present study, our aim was to determine the effects of aqueous (AAM) and ethanol (EAM) extracts of A. mellea on lipopolysaccharide (LPS)-induced inflammatory response by measuring the inducible nitric oxide synthase (iNOS), cyclooxygenase-1 and -2 (COX-1 and COX-2) protein expression, cytokines (TNF-alpha, IL-4 and IL-8) formation, nitric oxide (NO) release and prostaglandin (PGE(2)) production in human monocytic (THP-1) cells. At concentration of 100 microg/ml, EAM, but not AAM, effectively protected against LPS-induced cell death in THP-1 cells. At concentrations of 10 approximately 100 microg/ml, EAM showed a potent anti-inflammatory activity as demonstrated by a dose-dependent inhibition of LPS (1 microg/ml)-induced release of NO and PGE(2), and significantly decreased the transcription of proinflammatory cytokines. EAM at 100 mug/ml significantly blocked the LPS induction of iNOS and COX-2 expression, but not COX-1. Therefore, the protective effect of EAM against LPS-induced inflammatory mediators release could explain, at least in part, its effectiveness in alleviating certain inflammatory related diseases.

• Authors: Shu-Jing Wu, Jenn-Yi Tsai, Min-Nan Lai, Lean-Teik Ng
• Journal: The American journal of Chinese medicine (Am J Chin Med) Vol. 35 Issue 3 Pg. 507-16 ( 2007) ISSN: 0192-415X [Print] Singapore
• PMID: 17597509 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Inflammatory Agents
• Cytokines
• Drugs, Chinese Herbal
• Nitric Oxide
• Nitric Oxide Synthase
• Cyclooxygenase 1
• Cyclooxygenase 2
• Dinoprostone

Topics

• Agaricales
• Anti-Inflammatory Agents (pharmacology)
• Cell Line
• Cell Survival (drug effects)
• Cyclooxygenase 1 (drug effects, metabolism)
• Cyclooxygenase 2 (drug effects)
• Cytokines (antagonists & inhibitors, metabolism)
• Dinoprostone (antagonists & inhibitors, metabolism)
• Drugs, Chinese Herbal
• Humans
• Nitric Oxide (antagonists & inhibitors, metabolism)
• Nitric Oxide Synthase (antagonists & inhibitors, metabolism)
• Up-Regulation