Abstract
Background:
3-(3-chloro-phenyl)-5-(4-pyridyl)-4,5-dihydroisoxazole (DIC) is a five-membered heterocyclic compound containing a N-O bond. The anti-inflammatory effects of this compound were studied both in vitro and in vivo.
Principal findings:
DIC effectively decreased TNF-α and IL-6 release from LPS-stimulated macrophages in a dose dependent manner. DIC diminished the levels of COX-2 with subsequent inhibition of PGE(2) production. DIC also compromised HMGB1 translocation from the nucleus to the cytoplasm. Moreover, DIC prevented the nuclear translocation of NF-κB and inhibited the MAPK pathway. In vivo, DIC inhibited migration of neutrophils to the peritoneal cavity of mice.
Conclusions:
This study presents the potential utilization of a synthetic compound, as a lead for the development of novel anti-inflammatory drugs.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Active Transport, Cell Nucleus / drug effects
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Animals
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Anti-Inflammatory Agents / administration & dosage
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Anti-Inflammatory Agents / chemical synthesis
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Anti-Inflammatory Agents / pharmacology*
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Cell Movement / drug effects
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Cell Movement / immunology
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Dinoprostone / biosynthesis
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Enzyme Activation / drug effects
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Female
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HMGB1 Protein / metabolism
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Interleukin-6 / biosynthesis
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Isoxazoles / administration & dosage
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Isoxazoles / chemical synthesis
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Isoxazoles / pharmacology*
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Lipopolysaccharides / immunology
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Macrophages / drug effects
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Macrophages / immunology
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Mice
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Mice, Inbred BALB C
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Mitogen-Activated Protein Kinases / metabolism
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NF-kappa B / metabolism
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Peritonitis / chemically induced
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Peritonitis / drug therapy
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Pyridines / administration & dosage
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Pyridines / chemical synthesis
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Pyridines / pharmacology*
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Signal Transduction
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Thioglycolates / adverse effects
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Tumor Necrosis Factor-alpha / biosynthesis
Substances
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3-(3-chloro-phenyl)-5-(4-pyridyl)-4,5-dihydroisoxazole
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Anti-Inflammatory Agents
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HMGB1 Protein
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Interleukin-6
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Isoxazoles
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Lipopolysaccharides
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NF-kappa B
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Pyridines
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Thioglycolates
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Tumor Necrosis Factor-alpha
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Mitogen-Activated Protein Kinases
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Dinoprostone