Abstract
During endotoxemia, the ATP-dependent drug efflux pump P-glycoprotein (Abcb1/P-gp) is upregulated in kidney proximal tubule epithelial cells. The signaling pathway through which lipopolysaccharide (LPS) or tumor necrosis factor-alpha (TNF-alpha) regulates P-gp expression and activity was investigated further in the present study. Exposure of rat kidney proximal tubule cells to TNF-alpha alone or TNF-alpha and LPS increased P-gp gene and protein expression levels and efflux activity, suggesting de novo P-gp synthesis. Upon exposure to TNF-alpha in combination with LPS, P-gp activity in renal proximal tubule cells is increased under influence of nitric oxide (NO) produced by inducible NO synthase. Upon exposure to TNF-alpha alone, P-gp upregulation seems to involve TLR4 activation and nuclear factor kappaB (NF-kappaB) translocation, a pathway that is likely independent of NO. These findings indicate that at least two pathways regulate P-gp expression in the kidney during endotoxemia.
Original language | English |
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Pages (from-to) | 525180 |
Journal | Journal of Biomedicine and Biotechnology |
Volume | 2010 |
DOIs | |
Publication status | Published - 2010 |
Keywords
- Animals
- Cell Line
- Dose-Response Relationship, Drug
- Drug Combinations
- Epithelial Cells
- Gene Expression Regulation
- Kidney Tubules, Proximal
- Lipopolysaccharides
- P-Glycoprotein
- Rats
- Tumor Necrosis Factor-alpha