CDr10b inhibits the expression of cyclooxygenase-2 and inducible nitric oxide synthase induced by lipopolysaccharide

The pathophysiological processes of inflammation can lead to a host of diseases, such as periodontitis, atherosclerosis, rheumatoid arthritis, and even cancer. The dysregulated inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) activation play important roles in the development of c...

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Veröffentlicht in:European journal of pharmacology 2014-11, Vol.742, p.42-46
Hauptverfasser: Gu, Gyo-Jeong, Lim, Se-Jin, Ahn, Sang-il, Lee, Sung-Chan, Chang, Young-Tae, Choi, Tae Hyun, Kim, Byoung Soo, Eom, Yong-Bin, Lee, Na Kyung, Youn, Hyung-Sun
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Sprache:eng
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Zusammenfassung:The pathophysiological processes of inflammation can lead to a host of diseases, such as periodontitis, atherosclerosis, rheumatoid arthritis, and even cancer. The dysregulated inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) activation play important roles in the development of certain inflammatory diseases. Here, we investigated the effects of CDr10b which is originally developed for a microglia staining probe on inflammation, by modulating NF-κB activation and iNOS and COX-2 expression induced by lipopolysaccharide (LPS) in murine macrophages. The CDr10b suppressed NF-κB activation and iNOS and COX-2 expression induced by LPS. All the results suggest that CDr10b is a promising novel agent for the treatment of inflammatory diseases. [Display omitted]
ISSN:0014-2999
1879-0712
DOI:10.1016/j.ejphar.2014.08.036