Effect of high-intensity interval exercise on metformin pharmacokinetics in healthy men, assessed through a population pharmacokinetic model.

IF 7.7 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Stefanos Nikolaidis, Ioannis Kosmidis, Stylianos Papadopoulos, Artemis Lioupi, Marita Gandanidou, Helen Gika, Aristides Dokoumetzidis, Georgios Theodoridis, Vassilis Mougios
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Abstract

Background and purpose: Metformin and exercise are first-line therapies for prediabetes and type 2 diabetes. However, it is unclear whether the combination of metformin and exercise is synergistic or antagonistic. The aim of this study was to investigate the effect of exercise on metformin pharmacokinetics and help clarify the contradictory outcomes regarding the combination of metformin and exercise.

Experimental approach: Nine healthy men completed three 24-h sessions. In all sessions, participants received a single oral dose of 1000 mg metformin. In two of the sessions, they performed a high-intensity interval exercise test, 0.75 h (session A) or 4.65 h (session B), after metformin administration; they performed no exercise in the third session (reference). Venous blood samples were collected pre-dose and at 0.66, 1.4, 2.1, 2.5, 3, 3.5, 4, 4.5, 5.3, 6, 6.5, 7, 8, 10, 12 and 24 h after metformin administration. Non-compartmental pharmacokinetic analysis was performed, and a population pharmacokinetic (PopPK) model was constructed to detect covariates for explaining inter-individual and inter-occasion variability (IOV).

Key results: Significant differences were found between sessions for all pharmacokinetic parameters except t1/2. The PopPK model showed that exercise in session A reduced apparent volume of distribution (V/F) and apparent total plasma clearance (CL/F) by 31% and 25%, respectively; exercise in session B reduced CL/F by 17%.

Conclusions and implications: Exercise affected metformin pharmacokinetics, leading to an increase in plasma metformin concentration and becoming a covariate that explains the IOV of metformin pharmacokinetics. Exercise should be performed during a specific time after metformin intake.

通过人群药代动力学模型评估高强度间歇运动对健康男性二甲双胍药代动力学的影响
背景与目的:二甲双胍和运动是糖尿病前期和2型糖尿病的一线治疗方法。然而,目前尚不清楚二甲双胍与运动联合使用是协同作用还是拮抗作用。本研究的目的是研究运动对二甲双胍药代动力学的影响,并帮助澄清关于二甲双胍与运动结合的矛盾结果。实验方法:9名健康男性完成3个24小时的疗程。在所有的疗程中,参与者接受单次口服剂量1000mg二甲双胍。在两个疗程中,他们在服用二甲双胍后进行高强度间歇运动测试,0.75小时(a疗程)或4.65小时(B疗程);他们在第三期没有做任何运动(参考文献)。分别于给药前和给药后0.66、1.4、2.1、2.5、3、3.5、4、4.5、5.3、6、6.5、7、8、10、12和24 h采集静脉血。进行了非区室药代动力学分析,并构建了群体药代动力学(PopPK)模型,以检测解释个体间和环境间变异(IOV)的协变量。主要结果:各组间除t1/2外,所有药代动力学参数均有显著差异。PopPK模型显示,A期运动使表观分布容积(V/F)和表观总血浆清除率(CL/F)分别降低31%和25%;B阶段的锻炼减少了17%的CL/F。结论和意义:运动影响二甲双胍药代动力学,导致血浆二甲双胍浓度升高,成为解释二甲双胍药代动力学IOV的协变量。运动应在服用二甲双胍后的特定时间内进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
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