Literature DB >> 17949329

Triclosan inhibits uropathogenic Escherichia coli-stimulated tumor necrosis factor-alpha secretion in T24 bladder cells in vitro.

Chelsea N Elwood1, Ben H Chew, Shannon Seney, Jana Jass, John D Denstedt, Peter A Cadieux.   

Abstract

BACKGROUND AND
PURPOSE: Triclosan is an antimicrobial agent commonly used in consumer and medical products that inhibits bacterial fatty acid synthesis. In addition to its bactericidal effects, sublethal concentrations of triclosan reduce local inflammation, inhibit the growth of bacterial uropathogens, induce membrane stress, and inhibit P-fimbrial expression in uropathogenic Escherichia coli (UPEC). We tested whether sublethal concentrations of triclosan could reduce the adherence of UPEC to bladder and kidney cells and reduce the amount of the pro-inflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) produced by these cells during bacterial challenge in vitro.
MATERIALS AND METHODS: Assays of bacterial growth, adhesion, and intracellularization were performed using UPEC GR12 incubated for 4 hours on monolayers of human T24 bladder cells or A498 kidney cells with various sublethal concentrations of triclosan. The expression profile of TNF-alpha from bladder cells was evaluated using ELISA.
RESULTS: No significant decreases were observed in the adherence or invasion percentages of UPEC GR12 with either cell line when treated with sublethal amounts of triclosan. However, treatment with triclosan 0.5 microg/mL led to a significant decrease in the total number of UPEC GR12 recovered from T24 monolayers (P < 0.05). Importantly, a reduction in the expression of TNF-alpha by T24 cells was shown when UPEC GR12 was treated with triclosan (P < 0.05).
CONCLUSIONS: Sublethal concentrations of triclosan did not inhibit the adhesion or intracellularization of UPEC into kidney or bladder cell lines but did significantly reduce the amount of TNF-alpha secreted by bladder cells. Therefore, the use of triclosan on ureteral stents may prove clinically beneficial, not only by inhibiting bacterial survival and growth within the urinary tract, but by reducing local inflammation as well.

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Year:  2007        PMID: 17949329     DOI: 10.1089/end.2007.9903

Source DB:  PubMed          Journal:  J Endourol        ISSN: 0892-7790            Impact factor:   2.942


  7 in total

Review 1.  Current status of ureteral stent technologies: comfort and antimicrobial resistance.

Authors:  Carlos E Mendez-Probst; Alfonso Fernandez; John D Denstedt
Journal:  Curr Urol Rep       Date:  2010-03       Impact factor: 3.092

2.  Update on ureteral stent technology.

Authors:  Dirk Lange; Ben H Chew
Journal:  Ther Adv Urol       Date:  2009-08

3.  Urinary levels of triclosan and parabens are associated with aeroallergen and food sensitization.

Authors:  Jessica H Savage; Elizabeth C Matsui; Robert A Wood; Corinne A Keet
Journal:  J Allergy Clin Immunol       Date:  2012-06-15       Impact factor: 10.793

4.  Associations between urinary phenol and paraben concentrations and markers of oxidative stress and inflammation among pregnant women in Puerto Rico.

Authors:  Deborah J Watkins; Kelly K Ferguson; Liza V Anzalota Del Toro; Akram N Alshawabkeh; José F Cordero; John D Meeker
Journal:  Int J Hyg Environ Health       Date:  2014-11-18       Impact factor: 5.840

Review 5.  Ureteral stent symptoms and associated infections: a biomaterials perspective.

Authors:  Ben H Chew; Dirk Lange
Journal:  Nat Rev Urol       Date:  2009-07-14       Impact factor: 14.432

Review 6.  Ureteral stent technology: Drug-eluting stents and stent coatings.

Authors:  Luo Yang; Samantha Whiteside; Peter A Cadieux; John D Denstedt
Journal:  Asian J Urol       Date:  2015-09-21

Review 7.  Triclosan: An Update on Biochemical and Molecular Mechanisms.

Authors:  Mohammad A Alfhili; Myon-Hee Lee
Journal:  Oxid Med Cell Longev       Date:  2019-05-02       Impact factor: 6.543

  7 in total

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