Surge in expression of carboxylesterase 1 during the post-neonatal stage enables a rapid gain of the capacity to activate the anti-influenza prodrug oseltamivir.

BACKGROUND Oseltamivir, a widely used anti-influenza drug, is hydrolytically activated by carboxylesterase 1 (CES1). The expression of this carboxylesterase is developmentally regulated. This study was performed to determine when after birth infants acquire competence of activating this prodrug. METHODS Liver tissue samples were collected and divided into 5 age groups: group 1 (1-31 d old), group 2 (35-70 d old), group 3 (89-119 d old), group 4 (123-198 d old), and group 5 (>18 years of age). These samples were analyzed for oseltamivir hydrolysis and CES1 expression. RESULTS Liver samples in group 1 expressed the lowest level of CES1 with the lowest hydrolytic activity toward oseltamivir. A 4-7-fold increase between groups 1 and 2 (1-31 vs 35-70 d of age) was detected in the hydrolysis and expression analyses, respectively. Liver samples in the other 3 pediatric groups (35-198 d of age) exhibited similar expression and hydrolysis levels. Overall, liver samples in group 1 had CES1 expression and hydrolysis levels that were 10% of those of adults, whereas liver samples in the other 3 pediatric groups had levels that were ∼50% of adult levels. CONCLUSIONS The post-neonatal surge in CES1 expression ensures the hydrolytic capacity to be gained rapidly after birth in infants, but the larger variability during this period suggests that caution should be exercised on the extrapolated dosing regimens of ester drugs from other age groups.

[1]  J. Corton,et al.  Altered expression of the carboxylesterases ES-4 and ES-10 by peroxisome proliferator chemicals. , 2001, Toxicology.

[2]  J. Markowitz,et al.  Activation of the Antiviral Prodrug Oseltamivir Is Impaired by Two Newly Identified Carboxylesterase 1 Variants , 2009, Drug Metabolism and Disposition.

[3]  Jian Yang,et al.  Dexamethasone suppresses the expression of multiple rat carboxylesterases through transcriptional repression: evidence for an involvement of the glucocorticoid receptor. , 2008, Toxicology.

[4]  R. Davey,et al.  Pharmacokinetics and Tolerability of Oseltamivir Combined with Probenecid , 2008, Antimicrobial Agents and Chemotherapy.

[5]  Yan Jiang,et al.  Age- and Sex-Related Expression and Activity of Carboxylesterase 1 and 2 in Mouse and Human Liver , 2009, Drug Metabolism and Disposition.

[6]  Jian Yang,et al.  Antiplatelet Agents Aspirin and Clopidogrel Are Hydrolyzed by Distinct Carboxylesterases, and Clopidogrel Is Transesterificated in the Presence of Ethyl Alcohol , 2006, Journal of Pharmacology and Experimental Therapeutics.

[7]  William F Bosron,et al.  Human carboxylesterases: an update on CES1, CES2 and CES3. , 2009, Protein and peptide letters.

[8]  N. Dreyer,et al.  Effectiveness of antiviral treatment in human influenza A(H5N1) infections: analysis of a Global Patient Registry. , 2010, The Journal of infectious diseases.

[9]  T. Suga,et al.  Species differences in the induction of hepatic microsomal carboxylesterases caused by dietary exposure to di(2-ethylhexyl)phthalate, a peroxisome proliferator. , 1994, Drug metabolism and disposition: the biological fate of chemicals.

[10]  P. Ward,et al.  The Pharmacokinetics and Tolerability of the Oral Neuraminidase Inhibitor Oseltamivir (Ro 64–0796/GS4104) in Healthy Adult and Elderly Volunteers , 2000, Journal of clinical pharmacology.

[11]  E. Acosta,et al.  Oseltamivir dosing for influenza infection in premature neonates. , 2010, The Journal of infectious diseases.

[12]  Tetsuo Satoh,et al.  Structure, function and regulation of carboxylesterases. , 2006, Chemico-biological interactions.

[13]  H. Zhang,et al.  Dexamethasone differentially regulates expression of carboxylesterase genes in humans and rats. , 2000, Drug metabolism and disposition: the biological fate of chemicals.

[14]  Kaoru Kobayashi,et al.  Structural organization and characterization of the regulatory element of the human carboxylesterase (CES1A1 and CES1A2) genes. , 2008, Drug metabolism and pharmacokinetics.

[15]  Xiliang Wang,et al.  Pyrethroid insecticides: isoform-dependent hydrolysis, induction of cytochrome P450 3A4 and evidence on the involvement of the pregnane X receptor. , 2009, Toxicology and applied pharmacology.

[16]  P. Potter,et al.  Inhibition of carboxylesterase 1 is associated with cholesteryl ester retention in human THP-1 monocyte/macrophages. , 2008, Biochimica et biophysica acta.

[17]  Jian Yang,et al.  Interleukin-6 Alters the Cellular Responsiveness to Clopidogrel, Irinotecan, and Oseltamivir by Suppressing the Expression of Carboxylesterases HCE1 and HCE2 , 2007, Molecular Pharmacology.

[18]  T. Satoh,et al.  Effects of hypophysectomy and pituitary hormones on hepatic microsomal carboxylesterase isozymes in male rats. , 1988, Research communications in chemical pathology and pharmacology.

[19]  Yu-Jui Yvonne Wan,et al.  Human carboxylesterases HCE1 and HCE2: ontogenic expression, inter-individual variability and differential hydrolysis of oseltamivir, aspirin, deltamethrin and permethrin. , 2009, Biochemical pharmacology.

[20]  Sara K Quinney,et al.  Hydrolysis of irinotecan and its oxidative metabolites, 7-ethyl-10-[4-N-(5-aminopentanoic acid)-1-piperidino] carbonyloxycamptothecin and 7-ethyl-10-[4-(1-piperidino)-1-amino]-carbonyloxycamptothecin, by human carboxylesterases CES1A1, CES2, and a newly expressed carboxylesterase isoenzyme, CES3. , 2004, Drug metabolism and disposition: the biological fate of chemicals.

[21]  Christopher W. Wong,et al.  Oseltamivir ring prophylaxis for containment of 2009 H1N1 influenza outbreaks. , 2010, The New England journal of medicine.

[22]  B. Yan,et al.  Regulation of two rat liver microsomal carboxylesterase isozymes: species differences, tissue distribution, and the effects of age, sex, and xenobiotic treatment of rats. , 1994, Archives of biochemistry and biophysics.

[23]  D. Vance,et al.  Apolipoprotein B and triacylglycerol secretion in human triacylglycerol hydrolase transgenic mice Published, JLR Papers in Press, September 18, 2007. , 2007, Journal of Lipid Research.

[24]  F. Villarroya,et al.  Hepatic FGF21 expression is induced at birth via PPARalpha in response to milk intake and contributes to thermogenic activation of neonatal brown fat. , 2010, Cell metabolism.

[25]  F. Akhlaghi,et al.  Anti-Influenza Prodrug Oseltamivir Is Activated by Carboxylesterase Human Carboxylesterase 1, and the Activation Is Inhibited by Antiplatelet Agent Clopidogrel , 2006, Journal of Pharmacology and Experimental Therapeutics.

[26]  H. Skopnik,et al.  Oseltamivir for Treatment of Influenza in Infants Less Than One Year: A Retrospective Analysis , 2010, The Pediatric infectious disease journal.