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Author Notes:

Leonard L. Howell, PhD, Yerkes National Primate Research Center, Emory University, 954 Gatewood Rd., Atlanta, GA 30329 (USA), Tel. +1 404 727 7786, E-Mail lhowell@emory.edu

Subjects:

Research Funding:

This research was supported by DA10344 (L.L.H.), DA000517 (L.L.H.), T-32 DA015040 (E.K.S.), and RR00065 (Yerkes National Primate Research Center).

Keywords:

  • Fluoxetine
  • Norfluoxetine
  • Nonhuman primate
  • Pharmacokinetics
  • Selective serotonin reuptake inhibitors

Pharmacokinetics of Fluoxetine in Rhesus Macaques following Multiple Routes of Administration

Tools:

Journal Title:

Pharmacology

Volume:

Volume 88, Number 1-2

Publisher:

, Pages 44-49

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background/Aims Fluoxetine (Prozac) is a selective serotonin reuptake inhibitor currently used to treat depression and mood disorders. It has been widely studied clinically and preclinically, yet there is limited knowledge of its pharmacokinetics in nonhuman primates. Methods The present study characterized the pharmacokinetics of fluoxetine and its active metabolite norfluoxetine in rhesus macaques following both acute (1, 3, 5.6 and 10 mg/kg) and chronic doses (5.6 and 10 mg/kg/day) via different routes of administration (intravenous, subcutaneous, intramuscular, and oral). Blood samples were collected at multiple time points following administration and analyzed using mass spectrometry. Results Fluoxetine had a half-life of 11–16 h and norfluoxetine had a half-life of 21–29 h. Potentially functionally significant serum concentrations of norfluoxetine were present at 24 h even after a single administration of fluoxetine. Similar to observations in humans under steady state conditions, norfluoxetine accounted for the greater percentage of active drug in the blood stream. Conclusion A daily dose of 10 mg/kg administered orally maintained serum concentrations in the human clinical range over the course of 6 weeks. Given the long half-lives of fluoxetine and norfluoxetine observed in this study, precautions should be taken when designing preclinical studies to prevent accumulation of drug serum concentrations.

Copyright information:

© 2011 by S. Karger AG, Basel

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