کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5860334 | 1133179 | 2014 | 10 صفحه PDF | دانلود رایگان |
- The flame retardant FM 550 activates human PPARγ luciferase reporter assays.
- A non-monotonic concentration response relationship was identified for FM 550.
- The triarylphosphate components of FM 550 were responsible for PPARγ activation.
- Triphenyl phosphate was the most efficacious PPARγ ligand.
- The triarylphosphate components of FM 550 induced dose dependent apoptosis.
Firemaster® 550 (FM 550) is a mixture of brominated and triarylphosphate flame retardants used in polyurethane foam-based products. The primary components are also used in numerous other applications and are thus common household and industrial contaminants. Our previous animal studies suggested that FM 550 exposure may alter metabolism and cause weight gain. Employing human nuclear receptor (NR) luciferase reporter assays, the goal of this study was to evaluate the agonist actions of FM 550 and its constituent compounds at NRs with known roles in establishing or regulating energy balance. FM 550 was found to have significant agonist activity only at the master regulator of adipocyte differentiation PPARγ. As a result, the concentration response relationships and relative activities of FM 550 at PPARγ were investigated in more detail with the contribution of each chemical component defined and compared to the activities of the prototypical PPARγ environmental ligands triphenyltin and tributyltin. The resulting data indicated that the primary metabolic disruptive effects of FM 550 were likely mediated by the activity of the triarylphosphates at PPARγ, and have identified TPP as a candidate metabolic disruptor that also acts as a cytotoxicant.
Journal: Toxicology Letters - Volume 228, Issue 2, 15 July 2014, Pages 93-102