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替米沙坦与氢氯噻嗪对自发性高血压大鼠降压相互作用的药代动力学-药效学模型

Pharmacokinetic-pharmacodynamic model of the antihypertensive interaction between telmisartan and hydrochlorothiazide in spontaneously hypertensive rats.

作者信息

Hao Kun, Chen Yuancheng, Zhao Xiaoping, Liu Xiaoquan

机构信息

State Key Laboratory of Natural Medicines, Key Lab of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing, Jiangsu, China.

出版信息

J Pharm Pharmacol. 2014 Aug;66(8):1112-21. doi: 10.1111/jphp.12230. Epub 2014 Mar 17.

Abstract

OBJECTIVES

The goal of this study was to establish an integrated indirect response pharmacokinetic-pharmacodynamic model between telmisartan and hydrochlorothiazide to describe the antihypertensive interaction of these two drugs in spontaneously hypertensive rats.

METHODS

The blood pressure and plasma concentrations were measured by the tail-cuff test and high performance liquid chromatography-mass spectrometry, respectively, in spontaneously hypertensive rats. The current pharmacokinetic-pharmacodynamic model was based on the non-competitive pharmacodynamic interaction of two drugs acting on different physiological processes.

KEY FINDINGS

This model was able to acquire the temporal changes in drug concentration and blood pressure after administration of telmisartan or hydrochlorothiazide. The noncompetitive pharmacodynamic interaction assumed that the decreased blood pressure was attributed to the inhibitory function of telmisartan and stimulatory function of hydrochlorothiazide after administration of these two drugs. There was no significant pharmacokinetic change of telmisartan and hydrochlorothiazide in the different groups tested. The model predicted a synergistic pharmacodynamic interaction when telmisartan was administered in combination with hydrochlorothiazide, which was notably stronger than if the effects were additive.

CONCLUSION

The results showed that the presented pharmacokinetic-pharmacodynamic model was suitable for describing the antihypertensive interaction between telmisartan and hydrochlorothiazide.

摘要

目的

本研究的目的是建立替米沙坦和氢氯噻嗪之间的综合间接反应药代动力学-药效学模型,以描述这两种药物在自发性高血压大鼠中的降压相互作用。

方法

分别通过尾套法和高效液相色谱-质谱联用技术测量自发性高血压大鼠的血压和血浆浓度。当前的药代动力学-药效学模型基于两种作用于不同生理过程的药物的非竞争性药效学相互作用。

主要发现

该模型能够获取替米沙坦或氢氯噻嗪给药后药物浓度和血压的时间变化。非竞争性药效学相互作用假设,给药后血压下降归因于替米沙坦的抑制作用和氢氯噻嗪的刺激作用。在不同测试组中,替米沙坦和氢氯噻嗪的药代动力学没有显著变化。该模型预测,替米沙坦与氢氯噻嗪联合给药时存在协同药效学相互作用,其作用明显强于相加作用。

结论

结果表明,所提出的药代动力学-药效学模型适用于描述替米沙坦和氢氯噻嗪之间的降压相互作用。

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