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Research ArticleArticle

Neonatal Development of Hepatic UGT1A9: Implications of Pediatric Pharmacokinetics

Shogo J. Miyagi, Alison M. Milne, Michael W. H. Coughtrie and Abby C. Collier
Drug Metabolism and Disposition July 2012, 40 (7) 1321-1327; DOI: https://doi.org/10.1124/dmd.111.043752
Shogo J. Miyagi
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Alison M. Milne
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Michael W. H. Coughtrie
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Abby C. Collier
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Abstract

This article reports on the development of UDP-glucuronosyltransferase 1A9 (UGT1A9) in neonatal and pediatric liver. The substrate 4-methylumbelliferone (4MU) with specific inhibition by niflumic acid was used to define specific UGT1A9 activity. Subsequently, in silico pharmacokinetic (PK) and physiology-based pharmacokinetic (PBPK) modeling was used to determine UGT1A9 maturation and hepatic clearance. Modeled maximal enzyme activity was 27.9 nmol · min−1 · mg protein−1 at 4 months of age, which had high concordance with the average Vmax in 45 individual adult (>20 years) livers of 29.0 nmol · min−1 · mg protein−1. The activity of UGT1A9 ranged 7.5-fold in the adult population (4.1–54.5 nmol · min−1 · mg protein−1). Expression of UGT1A9 correlated with age only in children younger than 1 year (Spearman r = 0.70). Activity correlated with expression up to 18 years of age (Spearman r = 0.76). Furthermore, scaling intrinsic hepatic clearance of 4MU with an allometric PK model yielded a high clearance at birth and then fell to adult levels (1.3 l · h−1 · kg−1 at 18.1 years for well stirred or 1.4 l · h−1 · kg−1 at 18.7 years for parallel tube). The Simcyp PBPK models did not converge but showed an increase in clearance at under 1 year of age and then decreased to adult levels at approximately 20 years of age. Allometric scaling may be more accurate in cases of high-extraction drugs. Enzyme activities or hepatic clearances did not differ with gender or ethnicity. The UGT1A9 isoform has higher normalized clearance for 4MU at young ages, which may explain how other UGT1A9 substrates, such as propofol, have higher clearances in children than in adults.

Footnotes

  • This work was supported by the National Institutes of Health National Center for Research Resources [Grant RR024206] (Project 4); the Chun Foundation; and the Human Drug Conjugation Consortium (AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, F. Hoffman-La Roche, Lilly, Novartis, Pfizer, and Wyeth-Ayerst).

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

    http://dx.doi.org/10.1124/dmd.111.043752.

  • ABBREVIATIONS:

    PK
    pharmacokinetics
    UGT
    UDP-glucuronosyltransferase
    P450
    cytochrome P450
    4MU
    4-methylumbelliferone
    NFA
    niflumic acid
    PBPK
    physiology-based pharmacokinetics
    BSA
    bovine serum albumin
    ECL
    enhanced chemiluminescence
    MPPGL
    microsomal protein per gram of liver
    HSA
    human serum albumin
    SN-38
    7-ethyl-10-hydroxycamptothecin
    HEK
    human embryonic kidney
    CI
    confidence interval.

  • Received November 8, 2011.
  • Accepted April 5, 2012.
  • Copyright © 2012 by The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 40 (7)
Drug Metabolism and Disposition
Vol. 40, Issue 7
1 Jul 2012
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Research ArticleArticle

NEONATAL DEVELOPMENT OF HEPATIC UGT1A9

Shogo J. Miyagi, Alison M. Milne, Michael W. H. Coughtrie and Abby C. Collier
Drug Metabolism and Disposition July 1, 2012, 40 (7) 1321-1327; DOI: https://doi.org/10.1124/dmd.111.043752

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Research ArticleArticle

NEONATAL DEVELOPMENT OF HEPATIC UGT1A9

Shogo J. Miyagi, Alison M. Milne, Michael W. H. Coughtrie and Abby C. Collier
Drug Metabolism and Disposition July 1, 2012, 40 (7) 1321-1327; DOI: https://doi.org/10.1124/dmd.111.043752
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