ttCH, a selective inhibitor of inducible nitric oxide synthase expression with antiarthritic properties
European Journal of Pharmacology, ISSN: 0014-2999, Vol: 465, Issue: 1, Page: 183-189
2003
- 48Citations
- 16Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations48
- Citation Indexes48
- 48
- CrossRef28
- Captures16
- Readers16
- 16
Article Description
In a previous work, we investigated the effects of a series of dimethoxy- and trimethoxychalcone derivatives, with various patterns of fluorination, on nitric oxide production in lipopolysaccharide-stimulated murine RAW 264.7 cells. The present study was designed to determine if 2,4,6-trimethoxy-2′-trifluoromethylchalcone (ttCH) could modulate the production of nitric oxide (NO) and/or prostaglandins in vitro and in vivo. On the mouse macrophage cell line RAW 264.7, ttCH inhibited dose-dependently NO and prostaglandin E 2 production, with IC 50 in the micromolar range. This compound had no direct inhibitory effect on inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 activities. NO reduction was the consequence of inhibition of the expression of iNOS. This compound also exhibited in vivo an inhibitory behaviour on nitrite and prostaglandin E 2 levels. We have assessed the effect of ttCH in the treatment of acute and chronic inflammatory processes such as the mouse carrageenan paw oedema and the rat adjuvant-induced arthritis. The present study demonstrated that ttCH exerts acute and chronic anti-inflammatory effects that may be related with the inhibition of iNOS expression.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0014299903014572; http://dx.doi.org/10.1016/s0014-2999(03)01457-2; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0037470809&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/12650848; https://linkinghub.elsevier.com/retrieve/pii/S0014299903014572; http://linkinghub.elsevier.com/retrieve/pii/S0014299903014572; http://api.elsevier.com/content/article/PII:S0014299903014572?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0014299903014572?httpAccept=text/plain; http://dx.doi.org/10.1016/s0014-2999%2803%2901457-2; https://dx.doi.org/10.1016/s0014-2999%2803%2901457-2
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