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Research ArticleArticle

Functional Characterization of the Human Organic Cation Transporter 2 Variant p.270Ala>Ser

Oliver Zolk, Thomas F. Solbach, Jörg König and Martin F. Fromm
Drug Metabolism and Disposition June 2009, 37 (6) 1312-1318; DOI: https://doi.org/10.1124/dmd.108.023762
Oliver Zolk
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Thomas F. Solbach
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Jörg König
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Martin F. Fromm
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Abstract

The organic cation transporter 2 (OCT2, SLC22A2) plays an important role for renal drug elimination. Recent clinical studies indicate an impact of the frequent nonsynonymous c.808G>T (p.270Ala>Ser) polymorphism on renal clearance of metformin and the extent of the metformin-cimetidine interaction. The role of this polymorphism for renal disposition of endogenous compounds and drugs other than metformin has not been investigated. In addition, it is unclear whether the observed genotype dependence of an OCT2-mediated drug-drug interaction might occur also with other OCT inhibitors. To address these issues, we generated human embryonic kidney cells stably expressing wild-type OCT2 or the p.270Ala>Ser variant. No differences in protein expression levels and membrane incorporation pattern were observed between the two cell lines. The p.270Ala>Ser variant significantly impaired uptake kinetics of 1-methyl-4-phenylpyridinium, dopamine, norepinephrine, and propranolol. Vmax values were significantly reduced for uptake of all four compounds mediated by the p.270Ala>Ser variant compared with wild-type OCT2. In addition, a significant difference in the affinity to wild-type and mutant OCT2 was observed for dopamine (Km dopamine: 932 ± 77 versus 1285 ± 132 μM). Moreover, out of a set of 27 compounds p.270Ala>Ser OCT2 was significantly less sensitive to inhibition by cimetidine, flurazepam, metformin, mexiletine, propranolol, and verapamil than wild-type OCT2 (e.g., for propranolol: IC50 wild type versus p.270Ala>Ser 189 versus 895 μM, P < 0.001). Our results indicate that the common OCT2 c.808G>T single nucleotide polymorphism significantly alters uptake of endogenous compounds and drugs. Moreover, for selected compounds the extent of OCT2-mediated drug interactions could depend on OCT2 c.808G>T genotype.

Footnotes

  • This work was supported by the Deutsche Forschungsgemeinschaft (Fr 1298/5-1).

  • Article, publication date, and citation information can be found at http://dmd.aspetjournals.org.

  • doi:10.1124/dmd.108.023762.

  • ABBREVIATIONS: MPP+, 1-methyl-4-phenylpyridinium; OCT2, organic cation transporter 2; SNP, single nucleotide polymorphism; HEK, human embryonic kidney; GlpT, glycerol-3-phosphate transporter.

    • Received August 6, 2008.
    • Accepted February 26, 2009.
  • The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 37 (6)
Drug Metabolism and Disposition
Vol. 37, Issue 6
1 Jun 2009
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Research ArticleArticle

Functional Characterization of the Human Organic Cation Transporter 2 Variant p.270Ala>Ser

Oliver Zolk, Thomas F. Solbach, Jörg König and Martin F. Fromm
Drug Metabolism and Disposition June 1, 2009, 37 (6) 1312-1318; DOI: https://doi.org/10.1124/dmd.108.023762

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Research ArticleArticle

Functional Characterization of the Human Organic Cation Transporter 2 Variant p.270Ala>Ser

Oliver Zolk, Thomas F. Solbach, Jörg König and Martin F. Fromm
Drug Metabolism and Disposition June 1, 2009, 37 (6) 1312-1318; DOI: https://doi.org/10.1124/dmd.108.023762
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