Department of Pharmacy, 940th Hospital of Joint Logistic Support Force of Chinese People's Liberation Army, Lanzhou, China.
Curr Drug Metab. 2024;25(1):54-62. doi: 10.2174/0113892002277930240201101256.
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.
The objective of this study is to investigate the effect of a high altitude environment on PK and PD of warfarin in rats.
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.
Significant changes in PK behaviors and PD of warfarin in high altitude-rats were observed. Compared with the plain-rats, the peak concentration (C) 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.
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.
高海拔环境会影响药物的药代动力学(PK)参数,而 PK 参数是指导药物合理临床应用的重要理论基础。华法林是一种临床上常用的香豆素类口服抗凝剂,但它的治疗窗较窄,个体差异较大。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华法林在大鼠体内 PK 和 PD 的影响。
将大鼠随机分为平原组和高原组,给予 2mg/kg 华法林后经眶静脉丛采集血样。采用液相色谱-串联质谱法(LC-MS/MS)测定血浆样品中的华法林浓度,采用非房室模型法(WinNonlin 8.1 软件)计算 PK 参数。同时,采用 Western blot 法测定肝组织中 PXR、P-gp 和 CYP2C9 的表达。通过测定激活部分凝血活酶时间(APTT)和凝血酶原时间(PT)值,探索高海拔环境对华法林 PD 的影响,并根据 PT 计算国际标准化比值(INR)值。
高原大鼠的 PK 行为和 PD 发生了显著变化。与平原大鼠相比,高原大鼠的峰浓度(C)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,高海拔环境显著抑制了肝组织中 PXR、P-gp 和 CYP2C9 的表达。PD 研究结果表明,高海拔环境显著延长了 PT、APTT 和 INR 值。
高海拔环境抑制了大鼠对华法林的代谢,增加了其吸收,增强了抗凝效果,提示高海拔地区患者华法林的最佳剂量需要重新评估。