Pharmacokinetics of pergolide after intravenous administration to horses

被引:7
|
作者
Rendle, David I. [1 ]
Hughes, Kris J. [1 ]
Doran, Gregory S. [2 ]
Edwards, Scott H. [1 ]
机构
[1] Charles Sturt Univ, Sch Anim & Vet Sci, Wagga Wagga, NSW 2650, Australia
[2] Charles Sturt Univ, Graham Ctr Agr Innovat, Sch Agr & Wine Sci, Wagga Wagga, NSW 2650, Australia
关键词
PARS-INTERMEDIA DYSFUNCTION; EQUINE CUSHINGS-DISEASE; FUNCTIONAL POTENCIES; DOPAMINE AGONISTS; PLASMA; BIOAVAILABILITY; CYPROHEPTADINE; PREVALENCE; PROLACTIN; DRUGS;
D O I
10.2460/ajvr.76.2.155
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
OBJECTIVE To determine the pharmacokinetics of pergolide after IV administration to horses. ANIMALS 8 healthy adult horses. PROCEDURES Pergolide mesylate was administered IV at a dose of 20 mu g/kg (equivalent to 15.2 mu g of pergolide/kg) to each horse, and blood samples were collected over 48 hours. Pergolide concentrations in plasma were determined by means of high-performance liquid chromatography-tandem mass spectrometry, and pharmacokinetic parameters were determined on the basis of noncompartmental methods. RESULTS After IV administration of pergolide, mean +/- SD clearance, elimination half-life, and initial volume of distribution were 959 +/- 492 mL/h/kg, 5.64 +/- 2.36 hours, and 0.79 +/- 0.32 L/kg, respectively. CONCLUSIONS AND CLINICAL RELEVANCE With an elimination half-life of approximately 6 hours, twice-daily dosing may be more appropriate than once-daily dosing to reduce peak-trough fluctuation in pergolide concentrations. Further pharmacodynamic and pharmacokinetic studies of pergolide and its metabolites will be necessary to determine plasma concentrations that correlate with clinical effectiveness to determine the therapeutic range for the treatment of pituitary pars intermedia dysfunction.
引用
收藏
页码:155 / 160
页数:6
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