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苯妥英对兔体内阿霉素和阿霉素醇药代动力学的影响。

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

作者信息

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

机构信息

Clinical Pharmacology and Gerontology Research Unit, Veterans Administration Medical Center, Boise, Idaho.

出版信息

Cancer Chemother Pharmacol. 1988;22(4):294-8. doi: 10.1007/BF00254234.

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.

摘要

阿霉素通过普遍存在的醛酮还原酶广泛代谢为阿霉素醇。转化为这种醇代谢物的程度很重要,因为阿霉素醇可能是心脏毒性的主要促成因素。醛酮还原酶在体外被苯妥英抑制。本研究旨在考察苯妥英对阿霉素药代动力学的影响。在10只新西兰白兔中进行了阿霉素单剂量药代动力学研究,研究前以交叉方式用苯妥英或苯妥英溶媒(对照)输注,两次研究之间间隔4 - 6周。在阿霉素药代动力学研究开始前16小时及研究过程中开始输注。根据血浆苯妥英测定结果指导苯妥英输注,以维持血浆总浓度在20至30微克/毫升之间。静脉推注5毫克/千克阿霉素后,在32小时内间隔采集血样。通过高效液相色谱法测定血浆阿霉素和阿霉素醇浓度。血浆苯妥英平均浓度范围为17.4至33.9微克/毫升。苯妥英输注未改变阿霉素药代动力学。消除半衰期和分布容积与对照几乎相同。苯妥英给药期间阿霉素的清除率(60.9±5.8毫升/分钟/千克,平均值±标准误)与溶媒输注期间(67.5±5.4毫升/分钟/千克)相似。苯妥英给药与阿霉素醇消除半衰期从41.0±4.8小时显著降至25.6±2.8小时有关。阿霉素醇的血浆浓度/时间曲线下面积(AUC)从666.8±100.4显著降至491.5±65.7纳·小时·毫升-1。这些数据表明,临床相关浓度的苯妥英不会改变兔体内阿霉素向阿霉素醇的转化。苯妥英导致的阿霉素醇AUC降低似乎是由于阿霉素醇消除速率增加。苯妥英或类似药物可能通过诱导阿霉素醇代谢而非抑制醛酮还原酶来改变阿霉素醇的血浆浓度。

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