Uptake, Distribution and Release of 14C-Triclosan in Human Gingival Fibroblasts
Autor: | Manal Mustafa, Kjell Hultenby, Tülay Yucel-Lindberg, Biniyam Wondimu, Thomas Modéer |
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Rok vydání: | 2003 |
Předmět: |
Cell Nucleus
Cytoplasm Chemistry Cell Gingiva Pharmaceutical Science Fibroblasts Molecular biology Triclosan chemistry.chemical_compound medicine.anatomical_structure Biochemistry medicine Humans Liberation Carbon Radioisotopes Child Fibroblast Incubation Cells Cultured Intracellular Antibacterial agent |
Zdroj: | Journal of Pharmaceutical Sciences. 92:1648-1653 |
ISSN: | 0022-3549 |
DOI: | 10.1002/jps.10429 |
Popis: | Triclosan (2,4,4′-trichloro-2′-hydroxydiphenyl ether) is an antibacterial agent included in dentifrices and mouth rinses. Previously, we reported that triclosan reduces the production of the inflammatory mediators in gingival fibroblasts. The aim of this study was to investigate the uptake, distribution, and release of 14 C-triclosan in gingival fibroblasts. Time-course studies showed that the uptake of 14 C-triclosan in cytoplasmic and nuclear fraction started within the first minute of incubation, increased gradually, and reached constant levels after 1 h in the nuclear fraction and slightly increased in the cytoplasmic fraction between 3 and 24 h. The distribution of 14 C-triclosan in the cytoplasmic and the nuclear fractions was, on an average, 84 and 16%, respectively. Autoradiographic results based on transmission electron microscopy confirmed the distribution of 14 C-triclosan in the cytoplasm and nucleus of the cell. The release of 14 C-triclosan showed that the radioactivity of the agent in the medium gradually increased during the first hour of incubation and then reached steady-state levels. After repeated washing of preloaded fibroblasts, the level of 14 C-triclosan in the cytoplasmic fraction decreased by 77% whereas the level in the nuclear fraction remained unchanged. Our results demonstrate that triclosan is distributed in the cytoplasm and remains associated with the nucleus of gingival fibroblasts, suggesting that the agent may affect the intracellular signal pathways involved in the production of inflammatory mediators. © 2003 Wiley-Liss, Inc. and the American Pharmacists Association |
Databáze: | OpenAIRE |
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