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Induction of inducible nitric oxide synthase expression by 18β‐glycyrrhetinic acid in macrophages
Author(s) -
Jeong Hye Gwang,
Kim Ji Young
Publication year - 2002
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(02)02311-6
Subject(s) - transactivation , nitric oxide synthase , microbiology and biotechnology , transcription factor , electrophoretic mobility shift assay , luciferase , chemistry , gene expression , nitric oxide , transcription (linguistics) , glycyrrhizin , nf κb , nfkb1 , biochemistry , messenger rna , activator (genetics) , biology , gene , signal transduction , enzyme , transfection , linguistics , philosophy , organic chemistry , pharmacology
Glycyrrhizin (GL), a triterpenoid saponin fraction of licorice, is reported to have anti‐viral and anti‐tumor activities and is metabolized to 18β‐glycyrrhetinic acid (GA) in the intestine by intestinal bacteria. However, the mechanism underlying its effects is poorly understood. To further elucidate the mechanism of GA, the aglycone of GL, we investigated the effects of GA on the release of nitric oxide (NO) and at the level of inducible NO synthase (iNOS) gene expression in mouse macrophages. We found that GA elicited a dose‐dependent increase in NO production and in the level of iNOS mRNA. Since iNOS transcription has been shown to be under the control of the transcription factor nuclear factor κB (NF‐κB), the effects of GA on NF‐κB activation were examined. Transient expression assays with NF‐κB binding sites linked to the luciferase gene revealed that the increased level of iNOS mRNA, induced by GA, was mediated by the NF‐κB transcription factor complex. By using DNA fragments containing the NF‐κB binding sequence, GA was shown to activate the protein/DNA binding of NF‐κB to its cognate site, as measured by electrophoretic mobility shift assay. These results demonstrate that GA stimulates NO production and is able to up‐regulate iNOS expression through NF‐κB transactivation in macrophages.