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Effects of trovafloxacin on the IL-1-dependent activation of E-selectin in human endothelial cells in vitro.
- Source :
-
Immunopharmacology [Immunopharmacology] 2000 Jun; Vol. 48 (1), pp. 27-34. - Publication Year :
- 2000
-
Abstract
- E-selectin is an endothelial-specific surface protein, which is transiently expressed in response to inflammatory cytokines and plays an important role in the recruitment of leukocytes to the site of infection. The effect of two fluoroquinolones, ciprofloxacin (cipro) and trovafloxacin (trova), on the interleukin-1 (IL-1)-dependent activation of E-Selectin was studied on human umbilical vein endothelial cells (HUVEC) in vitro. Trova, at 80 microg/ml, affected the transient expression of E-selectin mRNA after pro-inflammatory stimulation with IL-1 leading to a sustained expression over 24 h. Surface expression of E-selectin remained upregulated after 24 h in a higher percentage of cells when they were activated in the presence of trova, as determined by flow cytometry analysis. Moreover, the concentration of shedded soluble E-selectin (sE-selectin) in the cell supernatant increased by 3.5 fold compared to those stimulated in the presence of cipro or without fluoroquinolones. Analogously, the antiproliferative effect of trova on endothelial cells was found to be more pronounced compared to cipro leading to an accumulation of cells arrested in G1-phase. These data provide evidence that accumulation of high concentration of trova in vivo in inflamed tissue might alter inflammatory responses.
- Subjects :
- Cell Division drug effects
Cell Membrane metabolism
Cells, Cultured
Ciprofloxacin pharmacology
Dose-Response Relationship, Drug
Endothelium, Vascular metabolism
Flow Cytometry
Humans
Propidium
RNA, Messenger biosynthesis
Time Factors
Anti-Infective Agents pharmacology
Cell Cycle drug effects
E-Selectin biosynthesis
Endothelium, Vascular drug effects
Fluoroquinolones
Interleukin-1 pharmacology
Naphthyridines pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0162-3109
- Volume :
- 48
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Immunopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 10822086
- Full Text :
- https://doi.org/10.1016/s0162-3109(99)00191-5