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二甲双胍在马体内的药代动力学和生物利用度

Pharmacokinetics and bioavailability of metformin in horses.

作者信息

Hustace Jaime L, Firshman Anna M, Mata John E

机构信息

Department of Clinical Sciences, College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331, USA.

出版信息

Am J Vet Res. 2009 May;70(5):665-8. doi: 10.2460/ajvr.70.5.665.

DOI:10.2460/ajvr.70.5.665
PMID:19405907
Abstract

OBJECTIVE

To determine pharmacokinetics and oral bioavailability of metformin in healthy horses.

ANIMALS

4 adult horses.

PROCEDURES

6 g of metformin was administered 3 times IV and PO (fed and unfed) to each horse, by use of a crossover design, with a 1-week washout period between treatments. Plasma metformin concentration was determined via high-pressure liquid chromatography.

RESULTS

Mean +/- SD distribution half-life of metformin following IV administration was 24.9 +/- 0.4 minutes with a volume of distribution of 0.3 +/- 0.1 L/kg. Mean area under the curve was 20.9 +/- 2.0 h.microg/mL for IV administration; PO administration resulted in area under the curves of 1.6 +/- 0.4 h.microg/mL in unfed horses and 0.8 +/- 0.2 h.microg/mL in fed horses. Bioavailability was determined to be approximately 7.1 +/- 1.5% in unfed horses and 3.9 +/- 1.0% in fed horses. The maximal concentration following PO administration in unfed horses was 0.4 +/- 0.1 microg/mL with a time at maximal concentration of 0.9 +/- 0.1 hours. In fed horses, maximal concentration was reduced to 0.3 +/- 0.04 microg/mL with a time at maximal concentration at 1.3 +/- 0.3 hours.

CONCLUSIONS AND CLINICAL RELEVANCE

The low bioavailability of metformin may explain the reported lack of clinical success in improving insulin sensitivity with metformin treatment in horses. Dosages and dose intervals previously used may have been insufficient to achieve plasma concentrations of drug comparable to the therapeutic range achieved in humans. Therefore, a larger and more frequently administered dose may be required to fully evaluate efficacy of metformin in horses.

摘要

目的

测定二甲双胍在健康马匹中的药代动力学和口服生物利用度。

动物

4匹成年马。

实验步骤

采用交叉设计,每匹马静脉注射和口服(进食和未进食状态下)3次二甲双胍,每次6克,每次治疗之间有1周的洗脱期。通过高压液相色谱法测定血浆二甲双胍浓度。

结果

静脉注射后二甲双胍的平均分布半衰期为24.9±0.4分钟,分布容积为0.3±0.1升/千克。静脉注射的平均曲线下面积为20.9±2.0小时·微克/毫升;口服给药在未进食马匹中的曲线下面积为1.6±0.4小时·微克/毫升,在进食马匹中为0.8±0.2小时·微克/毫升。未进食马匹的生物利用度约为7.1±1.5%,进食马匹为3.9±1.0%。未进食马匹口服给药后的最大浓度为0.4±0.1微克/毫升,最大浓度出现时间为0.9±0.1小时。在进食马匹中,最大浓度降至0.3±0.04微克/毫升,最大浓度出现时间为1.3±0.3小时。

结论及临床意义

二甲双胍的低生物利用度可能解释了报道中使用二甲双胍治疗马匹改善胰岛素敏感性缺乏临床成功的原因。之前使用的剂量和给药间隔可能不足以达到与人类治疗范围相当的血浆药物浓度。因此,可能需要更大且更频繁给药的剂量来全面评估二甲双胍在马匹中的疗效。

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