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Triclosan reduces microsomal prostaglandin E synthase‐1 expression in human gingival fibroblasts
Author(s) -
Mustafa M.,
Wondimu B.,
YucelLindberg T.,
KatsHallström A. T.,
Jonsson A. S.,
Modéer T.
Publication year - 2005
Publication title -
journal of clinical periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.456
H-Index - 151
eISSN - 1600-051X
pISSN - 0303-6979
DOI - 10.1111/j.1600-051x.2004.00622.x
Subject(s) - prostaglandin e2 , prostaglandin e , messenger rna , prostaglandin , triclosan , tumor necrosis factor alpha , microsome , chromosomal translocation , chemistry , cytokine , enzyme , radioimmunoassay , cyclooxygenase , microbiology and biotechnology , endocrinology , medicine , biology , biochemistry , gene , pathology
Objective: The effect of triclosan (2,4,4′‐trichloro‐2′‐hydroxydiphenyl ether) on the expression of cyclooxygenase‐2 (COX‐2) and microsomal prostaglandin E synthase‐1 (mPGES‐1) and on the translocation of the nuclear factor‐ κ B (NF‐ κ B) in relation to prostaglandin E 2 (PGE 2 ) production was investigated in human gingival fibroblasts challenged with tumor necrosis factor α (TNF α ). Methods: Fibroblasts were established from gingival biopsies obtained from six children. COX‐2 mRNA and protein expression was quantified using mRNA quantitation and enzyme immunometric assay kits. mPGES‐1 mRNA was analysed by RT‐PCR, mPGES‐1 protein and NF‐κB translocation by immunoblotting. PGE 2 was determined by radioimmunoassay. Results: The cytokine TNF α enhanced the expression of mRNA as well as the protein levels of both COX‐2 and mPGES‐1 and subsequently the production of PGE 2 in gingival fibroblasts. Treatment of gingival fibroblasts with triclosan (1 μ g/ml) significantly reduced the stimulatory effect of TNF α (10 ng/ml) on the expression of mPGES‐1 at both the mRNA and the protein level by an average of 21% and 43%, respectively, and subsequently the production of PGE 2 ( p <0.01). Triclosan did not, however, affect the translocation of NF‐ κ B or the expression of COX‐2 in TNF α‐ stimulated cells. Conclusion: The results show that triclosan reduces the augmented biosynthesis of PGE 2 by inhibiting the mRNA and the protein expression of mPGES‐1 in gingival fibroblasts. This finding may partly explain the anti‐inflammatory effect of the agent previously reported in clinical studies.