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γ-羟基丁酸在 6 周龄猪(Sus scrofa domesticus)静脉和口服给药后的药代动力学。

Pharmacokinetics of gamma-hydroxybutyric acid in 6-week-old swine (Sus scrofa domesticus) after intravenous and oral administration.

机构信息

Department of Large Animal Surgery, Anaesthesia and Orthopaedics, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

出版信息

J Vet Pharmacol Ther. 2024 Mar;47(2):95-106. doi: 10.1111/jvp.13418. Epub 2023 Nov 20.

Abstract

Sedative as well as protective effects during hypoxia have been described for gamma-hydroxybutyric acid (GHB). Six swine (Sus scrofa domesticus) of 6 weeks old were administered NaGHB at a dose of 500 mg/kg intravenously (IV) and 500 and 750 mg/kg orally (PO) in a triple cross-over design. Repeated blood sampling was performed to allow pharmacokinetic analysis of GHB. Whole blood concentration at time point 0 after IV administration was 1727.21 ± 280.73 μg/mL, with a volume of distribution of 339.45 ± 51.41 mL/kg and clearance of 164.94 ± 47.05 mL/(kg h). The mean peak plasma concentrations after PO administration were 326.57 ± 36.70 and 488.01 ± 154.62 μg/mL for 500 mg/kg and 750 mg/kg, respectively. These were recorded at 1.42 ± 0.72 and 1.58 ± 0.58 h after PO dose for GHB 500 mg/kg and 750 mg/kg, respectively. The elimination half-life for IV and PO 500 mg/kg and PO 750 mg/kg dose was respectively 1.33 ± 0.30, 1.16 ± 0.31 and 1.11 ± 0.33 h. The bioavailability (F) for PO administration was 45%. No clinical adverse effects were observed after PO administration. Deep sleep was seen in one animal after IV administration, other animals showed head pressing and ataxia.

摘要

γ-羟基丁酸(GHB)具有镇静和保护作用。在一项三交叉设计中,6 头 6 周龄的家猪(Sus scrofa domesticus)静脉内(IV)给予 500mg/kg 的 NaGHB 以及 500mg/kg 和 750mg/kg 的口服(PO)剂量。反复采血以允许进行 GHB 的药代动力学分析。IV 给药后 0 时间点的全血浓度为 1727.21±280.73μg/mL,分布容积为 339.45±51.41mL/kg,清除率为 164.94±47.05mL/(kg·h)。PO 给药后,500mg/kg 和 750mg/kg 的平均峰值血浆浓度分别为 326.57±36.70μg/mL 和 488.01±154.62μg/mL。这些分别在 PO 剂量后 1.42±0.72 和 1.58±0.58 h 记录,用于 GHB 500mg/kg 和 750mg/kg。IV 和 PO 500mg/kg 以及 PO 750mg/kg 剂量的消除半衰期分别为 1.33±0.30、1.16±0.31 和 1.11±0.33 h。PO 给药的生物利用度(F)为 45%。PO 给药后未观察到临床不良反应。一只动物在 IV 给药后出现深度睡眠,其他动物出现头部按压和共济失调。

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