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口服甘草酸对泼尼松龙药代动力学的影响。

Effect of oral administration of glycyrrhizin on the pharmacokinetics of prednisolone.

作者信息

Chen M F, Shimada F, Kato H, Yano S, Kanaoka M

机构信息

First Department of Internal Medicine, Toyama Medical and Pharmaceutical University, Japan.

出版信息

Endocrinol Jpn. 1991 Apr;38(2):167-74. doi: 10.1507/endocrj1954.38.167.

Abstract

The pharmacokinetics of total and free prednisolone (PSL) in six healthy men, with or without pretreatment with oral glycyrrhizin (GL), was investigated to confirm whether oral administration of GL influences the metabolism of PSL in man. Each subject received an intravenous administration of 0.096 mg/kg of prednisolone hemisuccinate (PSL-HS) with or without pretreatment with 50 mg of oral GL four times. Blood samples were taken from a peripheral vein at 5, 10, 15, 30, 45 min and 1, 1.5, 2, 3, 4, 6, 8, 10, 12 and 24 h after the start of PSL-HS infusion. The concentrations of total PSL in plasma were analyzed by high-performance liquid chromatography, and the free PSL was measured by an isocolloidosmolar equilibrium dialysis method. The pharmacokinetic parameters of PSL were determined by non-compartment analysis. Oral administration of GL was found to significantly increase the concentrations of total PSL at 6, 8 h, and of free PSL at 4, 6 and 8 h after PSL-HS infusion. Moreover, oral administration of GL was also found to modify the pharmacokinetics of both total and free PSL. After oral administration of GL, the area under the curve (AUC) was significantly increased, the total plasma clearance (CL) was significantly decreased, and the mean residence time (MRT) was significantly prolonged. However, the volume of distribution (Vdss) showed no evident change. This suggests that oral administration of GL increases the plasma PSL concentrations and influences its pharmacokinetics by inhibiting its metabolism, but not by affecting its distribution.

摘要

研究了6名健康男性在口服甘草酸(GL)预处理与否的情况下,泼尼松龙(PSL)总浓度和游离浓度的药代动力学,以确定口服GL是否会影响人体中PSL的代谢。每位受试者接受4次静脉注射0.096 mg/kg泼尼松龙半琥珀酸酯(PSL-HS),其中2次进行50 mg口服GL预处理,2次不进行预处理。在PSL-HS输注开始后的5、10、15、30、45分钟以及1、1.5、2、3、4、6、8、10、12和24小时,从外周静脉采集血样。通过高效液相色谱法分析血浆中总PSL的浓度,采用等胶体渗透压平衡透析法测定游离PSL的浓度。PSL的药代动力学参数通过非房室分析确定。结果发现,口服GL可显著提高PSL-HS输注后6、8小时总PSL的浓度以及4、6和8小时游离PSL的浓度。此外,口服GL还会改变总PSL和游离PSL的药代动力学。口服GL后,曲线下面积(AUC)显著增加,血浆总清除率(CL)显著降低,平均驻留时间(MRT)显著延长。然而,分布容积(Vdss)没有明显变化。这表明口服GL可提高血浆PSL浓度,并通过抑制其代谢而非影响其分布来影响其药代动力学。

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