Literature DB >> 3168142

Effect of phenytoin on the pharmacokinetics of doxorubicin and doxorubicinol in the rabbit.

B J Cusack1, D A Tesnohlidek, V L Loseke, R E Vestal, D E Brenner, R D Olson.   

Abstract

Doxorubicin is metabolized extensively to doxorubicinol by the ubiquitous aldoketoreductase enzymes. The extent of conversion to this alcohol metabolite is important since doxorubicinol may be the major contributor to cardiotoxicity. Aldoketoreductases are inhibited in vitro by phenytoin. The present study was conducted to examine the effect of phenytoin on doxorubicin pharmacokinetics. Doxorubicin single-dose pharmacokinetic studies were performed in 10 New Zealand White rabbits after pretreatment with phenytoin or phenytoin vehicle (control) infusions in crossover fashion with 4-6 weeks between studies. Infusions were commenced 16 h before and during the course of the doxorubicin pharmacokinetic studies. Phenytoin infusion was guided by plasma phenytoin estimation to maintain total plasma concentrations between 20 and 30 micrograms/ml. Following doxorubicin 5 mg/kg by i.v. bolus, blood samples were obtained at intervals over 32 h. Plasma doxorubicin and doxorubicinol concentrations were measured by HPLC. The mean plasma phenytoin concentrations ranged from 17.4 to 33.9 micrograms/ml. Phenytoin infusion did not alter doxorubicin pharmacokinetics. The elimination half-life and volume of distribution were almost identical to control. Clearance of doxorubicin during phenytoin administration (60.9 +/- 5.8 ml/min per kg, mean +/- SE) was similar to that during vehicle infusion (67.5 +/- 5.4 ml/min per kg). Phenytoin administration was associated with a significant decrease in doxorubicinol elimination half-life from 41.0 +/- 4.8 to 25.6 +/- 2.8 h. The area under the plasma concentration/time curve (AUC) for doxorubicinol decreased significantly from 666.8 +/- 100.4 to 491.5 +/- 65.7 n.h.ml-1. These data suggest that phenytoin at clinically relevant concentrations does not alter the conversion of doxorubicin to doxorubicinol in the rabbit. The reduction in the AUC for doxorubicinol caused by phenytoin appears to be due to an increased rate of doxorubicinol elimination. Phenytoin or similar agents may have the effect of modifying doxorubicinol plasma concentrations by induction of doxorubicinol metabolism rather than by inhibition of aldoketoreductase enzymes.

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Year:  1988        PMID: 3168142     DOI: 10.1007/bf00254234

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  25 in total

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Journal:  Biochem Pharmacol       Date:  1976-02-01       Impact factor: 5.858

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Journal:  Biochem Pharmacol       Date:  1978       Impact factor: 5.858

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Journal:  Res Commun Chem Pathol Pharmacol       Date:  1984-01

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Authors:  J H Peters; G R Gordon; D Kashiwase; E M Acton
Journal:  Cancer Chemother Pharmacol       Date:  1981       Impact factor: 3.333

7.  Superoxide anion production by adriamycinol from cardiac sarcosomes and by mitochondrial NADH dehydrogenase.

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Journal:  Anticancer Res       Date:  1986 Sep-Oct       Impact factor: 2.480

8.  Redox cycling of anthracyclines by cardiac mitochondria. II. Formation of superoxide anion, hydrogen peroxide, and hydroxyl radical.

Authors:  J H Doroshow; K J Davies
Journal:  J Biol Chem       Date:  1986-03-05       Impact factor: 5.157

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Journal:  J Clin Invest       Date:  1980-01       Impact factor: 14.808

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Authors:  P K Singal; G N Pierce
Journal:  Am J Physiol       Date:  1986-03
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  7 in total

1.  The effect of hepatic enzyme inducers on busulfan neurotoxicity and myelotoxicity.

Authors:  W E Fitzsimmons; R Ghalie; H Kaizer
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

2.  Doxorubicin pathways: pharmacodynamics and adverse effects.

Authors:  Caroline F Thorn; Connie Oshiro; Sharon Marsh; Tina Hernandez-Boussard; Howard McLeod; Teri E Klein; Russ B Altman
Journal:  Pharmacogenet Genomics       Date:  2011-07       Impact factor: 2.089

3.  Cardiac toxicity and antitumor activity of 4'-deoxy-4'-iodo-doxorubicinol.

Authors:  R Danesi; A Marchetti; N Bernardini; R V La Rocca; G Bevilacqua; M Del Tacca
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

4.  Effect of a low-protein diet on doxorubicin pharmacokinetics in the rabbit.

Authors:  B J Cusack; S P Young; V L Loseke; M R Hurty; L Beals; R D Olson
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

5.  Daunorubicin and daunorubicinol pharmacokinetics in plasma and tissues in the rat.

Authors:  B J Cusack; S P Young; R D Olson
Journal:  Cancer Chemother Pharmacol       Date:  1995       Impact factor: 3.333

6.  Doxorubicin and doxorubicinol pharmacokinetics and tissue concentrations following bolus injection and continuous infusion of doxorubicin in the rabbit.

Authors:  B J Cusack; S P Young; J Driskell; R D Olson
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

7.  Schisandrin B prevents doxorubicin-induced chronic cardiotoxicity and enhances its anticancer activity in vivo.

Authors:  Yang Xu; Zhen Liu; Jie Sun; Qiangrong Pan; Feifei Sun; Zhiyu Yan; Xun Hu
Journal:  PLoS One       Date:  2011-12-02       Impact factor: 3.240

  7 in total

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