The Effect of Exercise on Pharmacodynamics and Pharmacokinetics of a Single Dose of Unfractionated Heparin—A Randomized, Controlled, Crossover Study

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Cts-Clinical and Translational Science Pub Date : 2025-01-09 DOI:10.1111/cts.70113
Liva K. Stuhr, Joshua B. Feinberg, Thea Christoffersen, Konstantinos Dimopoulos, Mikkel B. Christensen, David P. Sonne, Troels Riis, Peter S. Plomgaard, Jens P. Goetze, Emil L. Larsen, Kristian Karstoft
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Abstract

Exercise increases blood and lymph flow in working muscles, potentially affecting the bioavailability and effect of subcutaneously administered drugs. The aim of this study was to assess the influence of a single exercise session on pharmacokinetics and pharmacodynamics of a single dose of subcutaneously administered unfractionated heparin. In a crossover design, 15 healthy males underwent four experimental days where 15,000 IU of unfractionated heparin was injected subcutaneously into the thigh of the non-dominant leg. Following the injection, one of four interventions was performed in randomized order on four separate occasions, each lasting 1 h: (1) no exercise, (2) double-legged exercise, (3) single-legged exercise with the non-dominant leg (where heparin was injected), and (4) single-legged exercise with the dominant leg. Blood was sampled during and after the interventions and analyzed for activated partial thromboplastin time (aPTT) and plasma heparin via an anti-factor Xa assay. The primary endpoint (maximum aPTT minus baseline aPTT) showed no statistically significant differences between interventions, nor did maximum minus baseline plasma heparin activities. However, after 1 h, change in aPTT was greater, following double-legged exercise compared with no exercise (mean difference 3.5 s, 95% CI 0.8–6.2) and greater after single-legged exercise with the non-dominant leg compared with the dominant (9.7 s, 3.9–15.5). Similar results were observed for plasma heparin activities. In conclusion, exercise does not affect the overall pharmacokinetics and pharmacodynamics of unfractionated heparin but tends to accelerate absorption and hence effect. The study thus underscores that physical exercise affects temporal uptake of subcutaneously administered therapy.

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运动对单剂量未分离肝素a药效学和药代动力学的影响:随机对照交叉研究。
运动增加工作肌肉的血液和淋巴流动,潜在地影响皮下给药的生物利用度和效果。本研究的目的是评估单次运动对单剂量皮下注射未分离肝素的药代动力学和药效学的影响。在交叉设计中,15名健康男性接受了为期4天的实验,在非优势腿的大腿皮下注射15,000 IU的未分离肝素。注射后,四种干预措施中的一种在四个不同的场合随机进行,每次持续1小时:(1)不运动,(2)双腿运动,(3)非优势腿单腿运动(注射肝素),(4)优势腿单腿运动。在干预期间和之后采集血液,并通过抗Xa因子测定分析活化的部分凝血活素时间(aPTT)和血浆肝素。主要终点(最大aPTT减去基线aPTT)在干预之间没有统计学上的显著差异,也没有最大血浆肝素活性减去基线。然而,1小时后,双足运动与不运动相比,aPTT的变化更大(平均差异为3.5秒,95% CI 0.8-6.2),单足运动与非优势腿相比,aPTT的变化更大(9.7秒,3.9-15.5)。血浆肝素活性也观察到类似的结果。综上所述,运动不影响未分离肝素的整体药代动力学和药效学,但倾向于加速吸收,从而加快效果。因此,该研究强调,体育锻炼影响皮下给药治疗的时间摄取。
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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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