Effects of P-glycoprotein inhibitors on transepithelial transport of cadmium in cultured renal epithelial cells, LLC-PK1 and LLC-GA5-COL 150.
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[1] Sarfaraz Ahmad,et al. Molecular handling of cadmium in transporting epithelia. , 2003, Toxicology and applied pharmacology.
[2] T. Endo,et al. Effects of P-glycoprotein inhibitors on cadmium accumulation in cultured renal epithelial cells, LLC-PK1, and OK. , 2002, Toxicology and applied pharmacology.
[3] L. Benet,et al. Comparison of Furosemide and Vinblastine Secretion from Cell Lines Overexpressing Multidrug Resistance Protein (P-Glycoprotein) and Multidrug Resistance-Associated Proteins (MRP1 and MRP2) , 2002, Pharmacology.
[4] H. Saitoh,et al. Secretory transport of cadmium through intestinal brush border membrane via H(+)-antiport. , 2000, Toxicology.
[5] D. Breimer,et al. Specificity of doxorubicin versus rhodamine-123 in assessing P-glycoprotein functionality in the LLC-PK1, LLC-PK1:MDR1 and Caco-2 cell lines. , 2000, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[6] P. Soares-da-Silva,et al. Outward transfer of dopamine precursor L-3,4-dihydroxyphenylalanine (L-dopa) by native and human P-glycoprotein in LLC-PK(1) and LLC-GA5 col300 renal cells. , 2000, The Journal of pharmacology and experimental therapeutics.
[7] F. Thévenod,et al. Up-regulation of Multidrug Resistance P-glycoprotein via Nuclear Factor-κB Activation Protects Kidney Proximal Tubule Cells from Cadmium- and Reactive Oxygen Species-induced Apoptosis* , 2000, The Journal of Biological Chemistry.
[8] T. Endo,et al. Further analysis of cadmium uptake from apical membrane of LLC-PK1 cells via inorganic anion exchanger. , 1999, Pharmacology & toxicology.
[9] T. Endo,et al. Bidirectional transport of cadmium across apical membrane of renal epithelial cell lines via H+-antiporter and inorganic anion exchanger. , 1998, Toxicology.
[10] Y. Ku,et al. Inhibitory Effects of a Cyclosporin Derivative, SDZ PSC 833, on Transport of Doxorubicin and Vinblastine via Human P‐Glycoprotein , 1998, Japanese journal of cancer research : Gann.
[11] T. Endo,et al. pH-dependent transport of cadmium in rat renal brush border membrane vesicles: cadmium efflux via H+-antiport. , 1998, Toxicology letters.
[12] D. Meijer,et al. Heterologous expression of various P-glycoproteins in polarized epithelial cells induces directional transport of small (type 1) and bulky (type 2) cationic drugs. , 1998, The Journal of pharmacology and experimental therapeutics.
[13] E Crivellato,et al. Handling of doxorubicin by the LLC-PK1 kidney epithelial cell line. , 1998, The Journal of pharmacology and experimental therapeutics.
[14] H. Saitoh,et al. Uptake of doxorubicin by cultured kidney epithelial cells LLC-PK1. , 1998, Biological & pharmaceutical bulletin.
[15] I. Yano,et al. Transport of quinolone antibacterial drugs by human P-glycoprotein expressed in a kidney epithelial cell line, LLC-PK1. , 1997, The Journal of pharmacology and experimental therapeutics.
[16] M. Cavet,et al. Fluoroquinolone (ciprofloxacin) secretion by human intestinal epithelial (Caco‐2) cells , 1997, British journal of pharmacology.
[17] F. Russel,et al. Rhodamine 123 accumulates extensively in the isolated perfused rat kidney and is secreted by the organic cation system. , 1997, European journal of pharmacology.
[18] T. Endo,et al. Comparison of cadmium uptakes from apical and basolateral membranes of LLC-PK1 cells. , 1996, Toxicology and applied pharmacology.
[19] Colin D. A. Brown,et al. Mediation of cimetidine secretion by P‐glycoprotein and a novel H+‐coupled mechanism in cultured renal epithelial monolayers of LLC‐PK1 cells , 1996, British journal of pharmacology.
[20] O. Yoshida,et al. Cepharanthin, a multidrug resistant modifier, is a substrate for P-glycoprotein. , 1995, The Journal of pharmacology and experimental therapeutics.
[21] K. Ullrich,et al. Specificity of transporters for 'organic anions' and 'organic cations' in the kidney. , 1994, Biochimica et biophysica acta.
[22] D. Miller,et al. Mechanisms mediating renal secretion of organic anions and cations. , 1993, Physiological reviews.
[23] Y. Tanigawara,et al. P‐glycoprotein‐mediated transcellular transport of MDR‐reversing agents , 1993, FEBS letters.
[24] Y. Tanigawara,et al. Human P-glycoprotein transports cyclosporin A and FK506. , 1993, The Journal of biological chemistry.
[25] R Hori,et al. Human P-glycoprotein transports cortisol, aldosterone, and dexamethasone, but not progesterone. , 1992, The Journal of biological chemistry.
[26] Y. Tanigawara,et al. Transport of digoxin by human P-glycoprotein expressed in a porcine kidney epithelial cell line (LLC-PK1). , 1992, The Journal of pharmacology and experimental therapeutics.
[27] K. White,et al. Photoaffinity labeling of the organic cation/H+ exchanger in renal brush border membrane vesicles. , 1992, The Journal of biological chemistry.
[28] I. Roninson,et al. Efficient inhibition of P-glycoprotein-mediated multidrug resistance with a monoclonal antibody. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[29] I. Pastan,et al. Transepithelial transport of vinblastine by kidney-derived cell lines. Application of a new kinetic model to estimate in situ Km of the pump. , 1990, Biochimica et biophysica acta.
[30] I. Pastan,et al. Heat shock and arsenite increase expression of the multidrug resistance (MDR1) gene in human renal carcinoma cells. , 1990, The Journal of biological chemistry.
[31] I. Pastan,et al. The multidrug transporter, a double-edged sword. , 1988, The Journal of biological chemistry.
[32] M C Willingham,et al. Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[33] I. Pastan,et al. The human multidrug resistance (mdr1) gene. cDNA cloning and transcription initiation. , 1987, The Journal of biological chemistry.
[34] L. Friberg,et al. Cadmium and the kidney. , 1984, Environmental health perspectives.
[35] M. M. Bradford. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.
[36] W. Prozialeck,et al. Surface binding and uptake of cadmium (Cd2+) by LLC-PK1 cells on permeable membrane supports , 2005, Archives of Toxicology.
[37] M. Melamed,et al. Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites. , 1989, Proceedings of the National Academy of Sciences of the United States of America.