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替米沙坦和氢氯噻嗪对自发性高血压大鼠长期给药后血压和血钾的药代动力学-药效学模型

The pharmacokinetic-pharmacodynamic model of telmisartan and hydrochlorothiazide on blood pressure and plasma potassium after long-term administration in spontaneously hypertensive rats.

作者信息

Yu Dan, Chen Yuancheng, Hao Kun

机构信息

Center for Drug Safety Evaluation and Research, Nanjing University of Chinese Medicine, Nanjing, 210023, China.

Institutes of Antibiotics, Huashan Hospital, Fudan University, Shanghai, 200040, China.

出版信息

Fundam Clin Pharmacol. 2015 Dec;29(6):543-52. doi: 10.1111/fcp.12152. Epub 2015 Oct 5.

Abstract

A pharmacokinetic-pharmacodynamic model was developed to describe the time course of blood pressure and plasma potassium after long-term telmisartan and/or hydrochlorothiazide administration in spontaneously hypertensive rats. The spontaneously hypertensive rats were administered once daily for 6 weeks. The drug concentration, blood pressure and plasma potassium were monitored for several points. The time courses of blood pressure and plasma potassium were described by indirect response pharmacokinetic-pharmacodynamic model. The synergistic antihypertensive pharmacodynamic interaction between telmisartan and hydrochlorothiazide was observed, which was simulated by the inhibitory function of telmisartan and stimulatory function of hydrochlorothiazide after co-administration of the two drugs. For plasma potassium, when hydrochlorothiazide administrated alone, the plasma potassium reached to a low steady-state level at 4.64 mmol/L for 6 weeks. The plasma potassium increased to a steady-state level at 4.84 mmol/L after co-administration of telmisartan. The time courses of plasma potassium were successfully characterized by indirect response pharmacokinetic-pharmacodynamic model after long-term administration of telmisartan and/or hydrochlorothiazide. The model captured turnovers of blood pressure and plasma potassium in the different time phases and dose conditions.

摘要

建立了一个药代动力学-药效学模型,以描述在自发性高血压大鼠中长期给予替米沙坦和/或氢氯噻嗪后血压和血钾的时间进程。对自发性高血压大鼠每日给药一次,持续6周。在多个时间点监测药物浓度、血压和血钾。血压和血钾的时间进程用间接反应药代动力学-药效学模型进行描述。观察到替米沙坦和氢氯噻嗪之间的协同降压药效学相互作用,这在两种药物联合给药后通过替米沙坦的抑制作用和氢氯噻嗪的刺激作用进行模拟。对于血钾,单独给予氢氯噻嗪时,血钾在6周内达到4.64 mmol/L的低稳态水平。联合给予替米沙坦后,血钾升至4.84 mmol/L的稳态水平。长期给予替米沙坦和/或氢氯噻嗪后,间接反应药代动力学-药效学模型成功地表征了血钾的时间进程。该模型捕捉了不同时间阶段和剂量条件下血压和血钾的变化情况。

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