Abstract
The objectives of the study were to evaluate the effects of pregnancy on CYP3A and P-glycoprotein (P-gp) activities, as measured by disposition of midazolam and digoxin, respectively. Thirteen women received digoxin (0.25 mg p.o.) and midazolam (2 mg p.o.) in random order, separated by 1-2 weeks at 28-32 weeks gestation, and the same order was repeated at 6-10 weeks postpartum. Plasma and urine concentrations were determined by liquid chromatography-mass spectrometry and analyzed by noncompartmental methods. Midazolam CL/F(unbound) (593 +/- 237 l/min vs. 345 +/- 103 l/min; P = 0.007), digoxin CL(Renal, unbound) (272 +/- 45 ml/min vs. 183 +/- 37 ml/min; P < 0.002) and digoxin CL(secretion,) (unbound) (109 +/- 34 ml/min vs. 58 +/- 22 ml/min; P < 0.002) were higher during pregnancy than postpartum. These data are consistent with increased hepatic and/or intestinal CYP3A and renal P-gp activities during pregnancy.
Publication types
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Randomized Controlled Trial
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
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Adult
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Anesthetics, Intravenous / pharmacokinetics
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Anti-Anxiety Agents / pharmacokinetics
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Anti-Arrhythmia Agents / pharmacokinetics
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Area Under Curve
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Cardiotonic Agents / pharmacokinetics
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Creatinine / urine
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Cytochrome P-450 CYP3A / metabolism*
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Digoxin / blood
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Digoxin / pharmacokinetics*
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Digoxin / urine
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Enzyme Inhibitors / pharmacokinetics
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Female
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Gas Chromatography-Mass Spectrometry
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Genotype
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Humans
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Hypnotics and Sedatives / pharmacokinetics
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Midazolam / blood
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Midazolam / pharmacokinetics*
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Midazolam / urine
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Postpartum Period / metabolism*
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Pregnancy / metabolism*
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Pregnancy Trimester, Third / metabolism
Substances
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ATP Binding Cassette Transporter, Subfamily B, Member 1
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Anesthetics, Intravenous
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Anti-Anxiety Agents
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Anti-Arrhythmia Agents
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Cardiotonic Agents
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Enzyme Inhibitors
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Hypnotics and Sedatives
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Digoxin
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Creatinine
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Cytochrome P-450 CYP3A
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Midazolam