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(E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine inhibits Inducible Nitric Oxide Synthase Expression in RAW264.7 Macrophages Stimulated with Lipopolysaccharide  

Gu, Gyo-Jeong (Department of Medical Science, College of Medical Sciences, SoonChunHyang University)
Eom, Sang-Hoon (Department of Biomedical Laboratory Science, College of Medical Sciences, SoonChunHyang University)
Suh, Chang Won (Department of Chemistry, College of Natural Sciences, Soonchunhyang University)
Koh, Kwang Oh (Department of Chemistry, College of Natural Sciences, Soonchunhyang University)
Kim, Dae Young (Department of Chemistry, College of Natural Sciences, Soonchunhyang University)
Youn, Hyung-Sun (Department of Medical Science, College of Medical Sciences, SoonChunHyang University)
Abstract
Toll-like receptors (TLRs) play an important role for host defense against invading pathogens. TLR4 has been identified as the receptor for lipopolysaccharide (LPS), which is a cell wall component of gram-negative bacteria. The activation of TLR4 signaling by LPS leads to the activation of NF-${\kappa}B$ and the expression of pro-inflammatory gene products such as cytokines, inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2). To evaluate the therapeutic potential of (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine (NVPP), previously synthesized in our laboratory, NF-${\kappa}B$ activation and iNOS and COX-2 expression induced by LPS were examined. NVPP inhibited the activation of NF-${\kappa}B$ induced by LPS. NVPP also suppressed the iNOS expression induced by LPS but it did not suppress COX-2 expression induced by LPS. These results suggest that NVPP has the specific mechanism for anti-inflammatory responses.
Keywords
Cyclooxygenase-2; Lipopolysaccharide; NF-${\kappa}B$; Inducible nitric oxide synthase; (E)-1-(2-(2-nitrovinyl) phenyl)pyrrolidine;
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