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丙卡特罗在纯种马中的药代动力学。

Pharmacokinetics of procaterol in thoroughbred horses.

作者信息

Kusano K, Nomura M, Toju K, Ishikawa Y, Minamijima Y, Yamashita S, Nagata S

机构信息

Equine Department, Japan Racing Association, Minato, Tokyo, Japan.

Racehorse Hospital, Ritto Training Center, Japan Racing Association, Ritto, Shiga, Japan.

出版信息

J Vet Pharmacol Ther. 2016 Jun;39(3):264-70. doi: 10.1111/jvp.12272. Epub 2015 Nov 5.

Abstract

Procaterol (PCR) is a beta-2-adrenergic bronchodilator widely used in Japanese racehorses for treating lower respiratory disease. The pharmacokinetics of PCR following single intravenous (0.5 μg/kg) and oral (2.0 μg/kg) administrations were investigated in six thoroughbred horses. Plasma and urine concentrations of PCR were measured using liquid chromatography-mass spectrometry. Plasma PCR concentration following intravenous administration showed a biphasic elimination pattern. The systemic clearance was 0.47 ± 0.16 L/h/kg, the steady-state volume of the distribution was 1.21 ± 0.23 L/kg, and the elimination half-life was 2.85 ± 1.35 h. Heart rate rapidly increased after intravenous administration and gradually decreased thereafter. A strong correlation between heart rate and plasma concentration of PCR was observed. Plasma concentrations of PCR after oral administration were not quantifiable in all horses. Urine concentrations of PCR following intravenous and oral administrations were quantified in all horses until 32 h after administration. Urine PCR concentrations were not significantly different on and after 24 h between intravenous and oral administrations. These results suggest that the bioavailability of orally administrated PCR in horses is very poor, and the drug was eliminated from the body slowly based on urinary concentrations. This report is the first study to demonstrate the pharmacokinetic character of PCR in thoroughbred horses.

摘要

丙卡特罗(PCR)是一种β-2肾上腺素能支气管扩张剂,在日本赛马中广泛用于治疗下呼吸道疾病。在6匹纯种马中研究了单次静脉注射(0.5μg/kg)和口服(2.0μg/kg)后PCR的药代动力学。使用液相色谱-质谱法测量血浆和尿液中PCR的浓度。静脉注射后血浆PCR浓度呈现双相消除模式。全身清除率为0.47±0.16L/h/kg,稳态分布容积为1.21±0.23L/kg,消除半衰期为2.85±1.35h。静脉注射后心率迅速增加,随后逐渐下降。观察到心率与血浆PCR浓度之间存在强相关性。所有马匹口服给药后血浆中PCR浓度均无法定量。静脉注射和口服给药后,所有马匹在给药后32小时内尿液中PCR浓度均可定量。静脉注射和口服给药后24小时及之后,尿液中PCR浓度无显著差异。这些结果表明,马匹口服PCR的生物利用度非常低,并且根据尿液浓度,药物从体内消除缓慢。本报告是首次证明纯种马中PCR药代动力学特征的研究。

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