高海拔环境对大鼠华法林药代动力学和药效学的影响

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Current drug metabolism Pub Date : 2024-01-01 DOI:10.2174/0113892002277930240201101256
Xiaojing Zhang, Hongfang Mu, Yan Zhong, Rong Wang, Wenbin Li
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引用次数: 0

摘要

背景:高海拔环境会影响药物的药代动力学(PK)参数,而PK参数是指导临床合理用药的重要理论依据。华法林是临床常用的香豆素类口服抗凝药,但其治疗窗窄,个体差异大。然而,高海拔环境对华法林的PK和药效学(PD)的影响尚不清楚:本研究旨在探讨高海拔环境对大鼠服用华法林的 PK 和 PD 的影响:方法:将大鼠随机分为普通组和高海拔组,在给药 2 mg/kg 华法林后通过眼眶静脉丛采集血样。采用液相色谱-串联质谱法(LC-MS/MS)测定血浆中华法林的浓度,并利用WinNonlin 8.1软件通过非室模型计算PK参数。同时,还采用免疫印迹法测定了PXR、P-gp和CYP2C9在肝组织中的表达。通过测定活化部分凝血活酶时间(APTT)和凝血酶原时间(PT)值,并根据PT值计算国际归一化比率(INR)值,探讨高海拔环境对华法林PD的影响:结果:观察到高海拔大鼠体内华法林的 PK 行为和 PD 发生了显著变化。与普通大鼠相比,华法林的峰浓度(Cmax)和血浆浓度-时间曲线下面积(AUC)分别显著增加了50.9%和107.46%。同时,高海拔环境明显抑制了肝组织中 PXR、P-gp 和 CYP2C9 的表达。PD研究结果表明,高海拔环境明显延长了PT、APTT和INR值:结论:高海拔环境抑制了华法林在大鼠体内的代谢,增加了大鼠对华法林的吸收,提高了华法林的抗凝效果。
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Effect of High Altitude Environment on Pharmacokinetic and Pharmacodynamic of Warfarin in Rats.

Background: High altitude environment affects the pharmacokinetic (PK) parameters of drugs and the PK parameters are an important theoretical basis for guiding the rational clinical use of drugs. Warfarin is an oral anticoagulant of the coumarin class commonly used in clinical practice, but it has a narrow therapeutic window and wide individual variation. However, the effect of high altitude environment on PK and pharmacodynamic (PD) of warfarin is unclear.

Objective: The objective of this study is to investigate the effect of a high altitude environment on PK and PD of warfarin in rats.

Method: Rats were randomly divided into plain group and high altitude group and blood samples were collected through the orbital venous plexus after administration of 2 mg/kg warfarin. Warfarin concentrations in plasma samples were determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and PK parameters were calculated by the non-compartment model using WinNonlin 8.1 software. Meanwhile, the expression of PXR, P-gp and CYP2C9 in liver tissues was also determined by western blotting. The effect of high altitude environment on PD of warfarin was explored by measuring activated partial thromboplastin time (APTT) and prothrombin time (PT) values and then calculated international normalized ratio (INR) values based on PT.

Results: Significant changes in PK behaviors and PD of warfarin in high altitude-rats were observed. Compared with the plain-rats, the peak concentration (Cmax) and the area under the plasma concentration-time curve (AUC) increased significantly by 50.9% and 107.46%, respectively. At the same time, high altitude environment significantly inhibited the expression of PXR, P-gp and CYP2C9 in liver tissues. The results of the PD study showed that high altitude environments significantly prolonged PT, APTT and INR values.

Conclusion: High altitude environment inhibited the metabolism and increased the absorption of warfarin in rats and increased the effect of anticoagulant effect, suggesting that the optimal dose of warfarin for patients at high altitude should be reassessed.

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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