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茶碱和二羟丙茶碱在马体内的药代动力学

Theophylline and dyphylline pharmacokinetics in the horse.

作者信息

Ayres J W, Pearson E G, Riebold T W, Chang S F

出版信息

Am J Vet Res. 1985 Dec;46(12):2500-6.

PMID:4083583
Abstract

The pharmacokinetics of theophylline and dyphylline were determined after IV administration in horses. In a preliminary experiment, the usual human dosage (milligram per kilogram) of each drug was given to 1 horse. Results were used to calculate dosages for a cross-over study, using 6 horses for each drug. Theophylline plasma concentrations decreased triexponentially in 5 of 6 healthy horses after IV infusion of 10 mg of aminophylline/kg of body weight for 16 to 32 minutes. In the 6 horses, total body elimination rate constants were variable, and the half-life of theophylline was 9.7 to 19.3 hours. Clearance was 42.3 to 69.2 ml/hr/kg. The initial distribution phase was rapid (t1/2 approx 3.5 to 4 minutes); a 2nd distribution phase was slower (t1/2 approx 1.5 to 2 hours). Plasma concentrations of theophylline were in the assumed effective range (10 to 20 micrograms/ml) from 15 minutes until 40 minutes after time zero. The mean apparent volume of distribution was 1.02 L/kg. After bolus IV injection of dyphylline (20 mg/kg), pharmacokinetics were best described by a 2-compartment open model in 2 horses and by a 3-compartment open model in 4 horses. In the 6 horses, elimination half-life of dyphylline was 1.9 to 2.9 hours, and clearance was 200 to 320 ml/hr/kg. Plasma concentrations (approx 50 micrograms/ml) were observed at 10 minutes after injection without adverse effects. Concentrations greater than 10 micrograms/ml were observed from time zero to about 1.5 hours after injection. Theophylline induced significant increases in heart rate, but dyphylline did not affect heart rate significantly.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在马静脉注射后测定了茶碱和二羟丙茶碱的药代动力学。在一项初步实验中,将每种药物的常用人类剂量(毫克/千克)给予1匹马。结果用于计算交叉研究的剂量,每种药物使用6匹马。静脉输注10毫克氨茶碱/千克体重16至32分钟后,6匹健康马中有5匹的茶碱血浆浓度呈三指数下降。在这6匹马中,全身消除速率常数各不相同,茶碱的半衰期为9.7至19.3小时。清除率为42.3至69.2毫升/小时/千克。初始分布阶段很快(t1/2约为3.5至4分钟);第二个分布阶段较慢(t1/2约为1.5至2小时)。从时间零点后15分钟到40分钟,茶碱的血浆浓度处于假定的有效范围(10至20微克/毫升)。平均表观分布容积为1.02升/千克。静脉推注二羟丙茶碱(20毫克/千克)后,2匹马的药代动力学最好用二室开放模型描述,4匹马用三室开放模型描述。在这6匹马中,二羟丙茶碱的消除半衰期为1.9至2.9小时,清除率为200至320毫升/小时/千克。注射后10分钟观察到血浆浓度(约50微克/毫升),无不良反应。从时间零点到注射后约1.5小时观察到浓度大于10微克/毫升。茶碱可显著增加心率,但二羟丙茶碱对心率无显著影响。(摘要截断于250字)

相似文献

1
Theophylline and dyphylline pharmacokinetics in the horse.茶碱和二羟丙茶碱在马体内的药代动力学
Am J Vet Res. 1985 Dec;46(12):2500-6.
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引用本文的文献

1
The pharmacokinetics of a slow-release theophylline preparation in horses after intravenous and oral administration.静脉注射和口服后,缓释型茶碱制剂在马体内的药代动力学。
Vet Res Commun. 1992;16(2):131-8. doi: 10.1007/BF01839010.