Quantifying Heart Rate Changes After Delta-9-Tetrahydrocannabinol Administration Using a PBPK-PD Model in Healthy Adults.

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2025-02-12 DOI:10.3390/pharmaceutics17020237
Lixuan Qian, Zhu Zhou
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Abstract

Background: As cannabis becomes legal in several U.S. states, the risk of THC-induced tachycardia increases. This study aimed to develop and verify a physiologically based pharmacokinetic-pharmacodynamic (PBPK-PD) model to assess the impact of THC and its active metabolite, 11-hydroxy-THC (11-OH-THC), on the heart rate of healthy adults. Methods: A PBPK-PD model for intravenous (IV) 11-OH-THC administration was first developed. Secondly, a PBPK-PD model for IV THC, combined with the metabolized 11-OH-THC, was established, verified, and validated. Direct PD models driven by the plasma, brain, and heart concentrations of THC and 11-OH-THC predicted using our previously verified PBPK model were tested for model development. Finally, the risks of tachycardia at a rest condition from various doses of oral and inhaled THC were simulated for 500 individuals aged 18-65 years, with a sex ratio of 1:1 and a baseline heart rate of 70 beats per minute. Results: The PD model was best described by a direct nonlinear Emax model driven by the sum of the total THC and 11-OH-THC concentrations in their effect compartments linked to their heart compartments. In 42 simulated dosing regimens with THC doses ranging from 2 to 69.4 mg, 97% of the observed heart rates or heart rate changes following THC administration fell within the 5th to 95th percentiles of the model-predicted values. Similarly, for two simulated 11-OH-THC IV doses, 93% of the observations fell within this range. Simulations indicated that half of the simulated population would experience tachycardia at doses of 60 mg and 15 mg of THC for oral and inhaled administration, respectively. The simulated risks of tachycardia based on specific conditions should be interpreted with caution. Conclusions: Our verified PBPK-PD model successfully describes the heart rate changes in healthy adults after IV, oral, and inhaled THC administration. This model provides a tool to predict the effects of THC and its primary metabolite on heart rates, offering valuable insights for assessing the risk of tachycardia in both clinical and recreational cannabis use.

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使用PBPK-PD模型量化健康成人δ -9-四氢大麻酚给药后的心率变化
背景:随着大麻在美国几个州合法化,四氢大麻酚诱发心动过速的风险增加。本研究旨在建立并验证基于生理的药代动力学-药效学(PBPK-PD)模型,以评估四氢大麻酚及其活性代谢物11-羟基四氢大麻酚(11-OH-THC)对健康成人心率的影响。方法:首先建立静脉给药(IV) 11-OH-THC PBPK-PD模型。其次,结合代谢的11-OH-THC,建立了IV THC的PBPK-PD模型,并进行了验证和验证。使用我们先前验证的PBPK模型预测的血浆、大脑和心脏中THC和11-OH-THC浓度驱动的直接PD模型进行了模型开发测试。最后,模拟了500名年龄在18-65岁、性别比例为1:1、基线心率为每分钟70次的个体在休息状态下,口服和吸入不同剂量四氢大麻酚的心动过速风险。结果:PD模型最好用直接非线性Emax模型来描述,该模型由与心脏室相连的效应室中总THC和11-OH-THC浓度的总和驱动。在42个四氢大麻酚剂量范围从2到69.4 mg的模拟给药方案中,97%的观察到的心率或四氢大麻酚给药后的心率变化落在模型预测值的第5到第95个百分位数之内。同样,对于两个模拟的11-OH-THC IV剂量,93%的观察值落在这个范围内。模拟表明,一半的模拟人群分别在口服和吸入THC剂量为60毫克和15毫克时出现心动过速。基于特定条件的模拟心动过速风险应谨慎解释。结论:我们验证的PBPK-PD模型成功地描述了健康成人在静脉、口服和吸入四氢大麻酚后的心率变化。该模型为预测四氢大麻酚及其主要代谢物对心率的影响提供了一种工具,为评估临床和娱乐大麻使用中心动过速的风险提供了有价值的见解。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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