RT Journal Article
SR Electronic
T1 Multidrug Resistance-Associated Protein 4 (MRP4/ABCC4) Controls Efflux Transport of Hesperetin Sulfates in SULT1A3-Overexpressing HEK293 Cells
JF Drug Metabolism and Disposition
JO Drug Metab Dispos
FD American Society for Pharmacology and Experimental Therapeutics
SP dmd.115.065953
DO 10.1124/dmd.115.065953
A1 Hua Sun
A1 Xiao Wang
A1 Xiaotong Zhou
A1 Danyi Lu
A1 Zhiguo Ma
A1 Baojian Wu
YR 2015
UL http://dmd.aspetjournals.org/content/early/2015/07/29/dmd.115.065953.abstract
AB Sulfonation is an important metabolic pathway for hesperetin. However, the mechanisms for cellular disposition of hesperetin and its sulfate metabolites are not fully established. In this study, disposition of hesperetin via the sulfonation pathway was investigated using HEK293 cells overexpressing sulfotransferase 1A3 (SULT1A3). Two mono-sulfates, hesperetin-3'-O-sulfate (H-3'-S) and hesperetin-7-O-sulfate (H-7-S), were rapidly generated and excreted into the extracellular compartment upon incubation of the cells with hesperetin. Regiospecific sulfonation of hesperetin by cell lysate followed the substrate inhibition kinetics (Vmax = 0.66 nmol/min/mg, Km = 12.9 μM and Ksi= 58.1 μM for H-3'-S; Vmax = 0.29 nmol/min/mg, Km = 14.8 μM and Ksi= 49.1 μM for H-7-S). The pan-MRP inhibitor MK-571 at 20 uM essentially abolished cellular excretion of both H-3'-S and H-7-S (the excretion activities were only 6% of the control), whereas the BCRP-selective inhibitor Ko143 had no effects on sulfate excretion. In addition, knock-down of MRP4 led to a substantial reduction (> 47.1%, p < 0.01) in sulfate excretion. Further, H-3'-S and H-7-S were good substrates for transport by MRP4 according to the vesicular transport assay. Moreover, sulfonation of hesperetin and excretion of its metabolites were well characterized by a two-compartment pharmacokinetic model that integrated drug uptake and sulfonation with MRP4-mediated sulfate excretion. In conclusion, the exporter MRP4 controlled efflux transport of hesperetin sulfates in HEK293 cells. Due to significant expression in the various organs/tissues (including the liver and kidney), MRP4 should be a determining factor to elimination and body distribution of hesperetin sulfates.