Abstract | AIM OF THIS STUDY: METHODS: RESULTS: YJB significantly decreased the production of peritoneal macrophages derived TNF-α, IL-1 and NO. YJB also significantly decreased prostaglandin E ( PGE) and upregulated the Bax expression in AA rat's synovium. CONCLUSION: YJB is a potential anti-rheumatic agent targeting the inflammatory and immunomodulatory response of macrophages while down regulating the PGE and up-regulating the pro-apoptotic Bax expression. Such characteristics of YJB on AA may be advantageous to the treatment of clinical rheumatoid arthritis.
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Authors | Pathirage Kamal Perera, Cheng Peng, Lv Xue, Yunman Li, Caifeng Han |
Journal | Journal of ethnopharmacology
(J Ethnopharmacol)
Vol. 134
Issue 1
Pg. 171-5
(Mar 08 2011)
ISSN: 1872-7573 [Electronic] Ireland |
PMID | 21134433
(Publication Type: Journal Article)
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Copyright | Copyright © 2010 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- Drugs, Chinese Herbal
- Interleukin-1
- Prostaglandins E
- Tumor Necrosis Factor-alpha
- bcl-2-Associated X Protein
- yi shen juan bi
- Nitric Oxide
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Topics |
- Animals
- Arthritis, Experimental
(drug therapy, metabolism)
- Blotting, Western
- Drugs, Chinese Herbal
(therapeutic use)
- Enzyme-Linked Immunosorbent Assay
- Interleukin-1
(antagonists & inhibitors, metabolism)
- Macrophages, Peritoneal
(drug effects, metabolism)
- Male
- Nitric Oxide
(metabolism)
- Prostaglandins E
(metabolism)
- Rats
- Rats, Sprague-Dawley
- Spectrophotometry, Ultraviolet
- Tumor Necrosis Factor-alpha
(antagonists & inhibitors, metabolism)
- bcl-2-Associated X Protein
(metabolism)
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