Source:http://linkedlifedata.com/resource/pubmed/id/19135346
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6-7
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pubmed:dateCreated |
2009-5-12
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pubmed:abstractText |
Madecassoside (MA), a triterpenoid product isolated from Centella asiatica, has been described to exhibit antioxidant and anti-inflammatory activities. The present study was undertaken to determine whether madecassoside (MA) is efficacious against collagen-induced arthritis (CIA) in mice and its possible mechanisms. DBA/1J mice were immunized with bovine type II collagen and treated with MA (3, 10 and 30 mg/kg d, i.g.) from days 21 to 42 after immunization. Arthritis was evaluated by hind paw swelling, polyarthritis index, and histological examination. In vitro proliferation of spleen cells was examined using 3-[4,5-dimethylthylthiazol-2-yl]-2, 5-diphenyltetrazoliumbromide (MTT) assay. Plasma levels of cytokines tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6), interleukin-10 (IL-10) and the expression of prostaglandin E(2) (PGE(2)), cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) in synovial tissues were also determined. The results showed that comparing with untreated CIA mice, treated with MA dose-dependently suppressed the clinical arthritis score and joints tissues pathological damage, reduced the proliferation of spleen cells, plasma levels of TNF-alpha and IL-6, synovial tissues PGE(2) production and COX-2 protein expression, however, the expression of COX-1 in synovial tissues did not change and the plasma levels of IL-10 were increased. These results suggest that MA can effectively alleviate inflammatory response on CIA, and anti-inflammatory effects of MA can be attributed, at least partially, to the inhibition of pro-inflammatory mediators, including COX-2 expression, PGE(2) production, TNF-alpha and IL-6 levels and the up-regulation anti-inflammatory molecule IL-10.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Inflammation Mediators,
http://linkedlifedata.com/resource/pubmed/chemical/Triterpenes,
http://linkedlifedata.com/resource/pubmed/chemical/madecassoside
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1618-095X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
538-46
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pubmed:meshHeading |
pubmed-meshheading:19135346-Animals,
pubmed-meshheading:19135346-Arthritis, Experimental,
pubmed-meshheading:19135346-Blotting, Western,
pubmed-meshheading:19135346-Cell Proliferation,
pubmed-meshheading:19135346-Cytokines,
pubmed-meshheading:19135346-Dinoprostone,
pubmed-meshheading:19135346-Inflammation,
pubmed-meshheading:19135346-Inflammation Mediators,
pubmed-meshheading:19135346-Male,
pubmed-meshheading:19135346-Mice,
pubmed-meshheading:19135346-Mice, Inbred DBA,
pubmed-meshheading:19135346-Synovial Membrane,
pubmed-meshheading:19135346-Triterpenes
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pubmed:year |
2009
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pubmed:articleTitle |
Madecassoside attenuates inflammatory response on collagen-induced arthritis in DBA/1 mice.
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pubmed:affiliation |
Department of Pharmacology, Chongqing Medical University, Chongqing 400016, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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