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Pharmacokinetics of isoflavones from soy infant formula in neonatal and adult rhesus monkeys.
Doerge, Daniel R; Woodling, Kellie A; Churchwell, Mona I; Fleck, Stefanie C; Helferich, William G.
Afiliación
  • Doerge DR; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA. Electronic address: daniel.doerge@fda.hhs.gov.
  • Woodling KA; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
  • Churchwell MI; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
  • Fleck SC; Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
  • Helferich WG; Department of Food Science and Human Nutrition, University of Illinois, Urbana-Champaign, IL 61810, USA.
Food Chem Toxicol ; 92: 165-76, 2016 Jun.
Article en En | MEDLINE | ID: mdl-27084109
ABSTRACT
Consumption of soy infant formula represents a unique exposure scenario in which developing children ingest a mixture of endocrine-active isoflavones along with a substantial portion of daily nutrition. Genistein and daidzein were administered as glucoside conjugates to neonatal rhesus monkeys in a fortified commercial soy formula at 5, 35, and 70 days after birth. A single gavage dosing with 10 mg/kg bw genistein and 6 mg/kg bw daidzein was chosen to represent the upper range of typical daily consumption and to facilitate complete pharmacokinetic measurements for aglycone and total isoflavones and equol. Adult monkeys were also gavaged with the same formula solution at 2.8 and 1.6 mg/kg bw genistein and daidzein, respectively, and by IV injection with isoflavone aglycones (5.2 and 3.2 mg/kg bw, respectively) to determine absolute bioavailability. Significant differences in internal exposure were observed between neonatal and adult monkeys, with higher values for dose-adjusted AUC and Cmax of the active aglycone isoflavones in neonates. The magnitude and frequency of equol production by the gut microbiome were also significantly greater in adults. These findings are consistent with immaturity of metabolic and/or physiological systems in developing non-human primates that reduces total clearance of soy isoflavones from the body.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Soja / Fórmulas Infantiles / Isoflavonas Límite: Adult / Animals / Humans / Infant / Male Idioma: En Revista: Food Chem Toxicol Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Soja / Fórmulas Infantiles / Isoflavonas Límite: Adult / Animals / Humans / Infant / Male Idioma: En Revista: Food Chem Toxicol Año: 2016 Tipo del documento: Article
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