Abstract
The anti-inflammatory activity of the surfactin C derived from Bacillus subtilis isolate was investigated in lipopolysaccharide (LPS, 1 microg ml(-1))-treated mouse RAW 264.7 cells. LPS increased mRNA transcription of cyclooxygenase (COX)-2, interleukin (IL)-1beta and inducible nitric oxide synthase (iNOS). However, surfactin C at 50 microg ml(-1 )inhibited the LPS-induced increase in the transcription of IL-1beta and iNOS and nitric oxide (NO) production in a dose-dependent manner.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Bacillus subtilis / chemistry*
-
Bacterial Proteins / chemistry
-
Bacterial Proteins / pharmacology*
-
Cell Line
-
Dose-Response Relationship, Drug
-
Gene Expression Regulation / drug effects*
-
Interleukin-1 / biosynthesis*
-
Interleukin-1 / genetics
-
Lipopeptides
-
Lipopolysaccharides / pharmacology
-
Mice
-
Nitric Oxide Synthase Type II / biosynthesis*
-
Nitric Oxide Synthase Type II / genetics
-
Peptides, Cyclic / chemistry
-
Peptides, Cyclic / pharmacology*
-
Transcription, Genetic / drug effects
Substances
-
Bacterial Proteins
-
Interleukin-1
-
Lipopeptides
-
Lipopolysaccharides
-
Peptides, Cyclic
-
surfactin peptide
-
Nitric Oxide Synthase Type II
-
Nos2 protein, mouse