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Research ArticleArticle

Selective Role of Sulfotransferase 2A1 (SULT2A1) in the N-Sulfoconjugation of Quinolone Drugs in Humans

Laddawan Senggunprai, Kouichi Yoshinari and Yasushi Yamazoe
Drug Metabolism and Disposition August 2009, 37 (8) 1711-1717; DOI: https://doi.org/10.1124/dmd.109.027441
Laddawan Senggunprai
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Kouichi Yoshinari
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Yasushi Yamazoe
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Abstract

N-Sulfoconjugation is a common metabolic pathway of amine compounds in vivo. In the present study, we investigated the N-sulfation of quinolones and other amine drugs (ciprofloxacin, moxifloxacin, garenoxacin, desipramine, and metoclopramide) to assess the contribution of specific human cytosolic sulfotransferases (SULTs) to the reactions using purified recombinant enzymes and human liver cytosols (HLCs). Among the enzymes examined, human (h) SULT2A1 exhibited N-sulfoconjugation activities toward all drugs tested, whereas the other five different forms (hSULT1A1, hSULT1A3, hSULT1B1, hSULT1C2, and hSULT1E1) showed no detectable activities except hSULT1A1 for garenoxacin sulfation. The N-sulfoconjugating activity of hSULT2A1 was highest toward moxifloxacin (6.3 ± 0.1 nmol/min/mg protein) at the substrate concentration of 100 μM. Kinetic analyses demonstrated that HLC-mediated N-sulfations were monophasic for all of the substrates examined with apparent Km values comparable to those mediated by hSULT2A1. The Km values for N-sulfation mediated by hSULT2A1 were as follows: 1.08 ± 0.03 mM for ciprofloxacin, 0.53 ± 0.01 mM for moxifloxacin, 0.19 ± 0.01 mM for garenoxacin, 0.054 ± 0.001 mM for desipramine, and 2.32 ± 0.12 mM for metoclopramide. The sulfating activities of HLCs toward the amines were well correlated with those for O-sulfation of dehydroepiandrosterone, a hSULT2A1 probe substrate. Taken together, the present results unequivocally demonstrate that hSULT2A1 is responsible for the N-sulfation of quinolones and possibly other therapeutic drugs in humans.

Footnotes

  • ↵1 The nomenclature of individual SULT forms is based on the Human Genome Nomenclature Committee. The names in the nomenclature system proposed by us with “ST” as a prefix (Nagata et al., 2005) are included in the text. Their accession numbers are as follows: ST1A3/hSULT1A1, NM_001055; ST1A5/hSULT1A3, NM_003166; ST1B2/hSULT1B1, NM_014465; ST1C2/hSULT1C2, NM_001056; ST1E4/hSULT1E1, NM_005420; and ST2A3/hSULT2A1, NM_003167.

  • This work was supported in part by the Ministry of Education, Culture, Sports, Sciences and Technology of Japan; and the Comprehensive Research and Education Center for Planning of Drug Development and Clinical Education, Tohoku University 21st Century “Center of Excellence” Program.

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

  • doi:10.1124/dmd.109.027441.

  • ABBREVIATIONS: SULT, sulfotransferase; PAPS, 3′-phosphoadenosine 5′-phosphosulfate; DHEA, dehydroepiandrosterone; h, human; HLC, human liver cytosol.

    • Accepted May 4, 2009.
    • Received March 12, 2009.
  • The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 37 (8)
Drug Metabolism and Disposition
Vol. 37, Issue 8
1 Aug 2009
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Research ArticleArticle

Selective Role of Sulfotransferase 2A1 (SULT2A1) in the N-Sulfoconjugation of Quinolone Drugs in Humans

Laddawan Senggunprai, Kouichi Yoshinari and Yasushi Yamazoe
Drug Metabolism and Disposition August 1, 2009, 37 (8) 1711-1717; DOI: https://doi.org/10.1124/dmd.109.027441

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Research ArticleArticle

Selective Role of Sulfotransferase 2A1 (SULT2A1) in the N-Sulfoconjugation of Quinolone Drugs in Humans

Laddawan Senggunprai, Kouichi Yoshinari and Yasushi Yamazoe
Drug Metabolism and Disposition August 1, 2009, 37 (8) 1711-1717; DOI: https://doi.org/10.1124/dmd.109.027441
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