School of Medicine, Jinan University, 601 Huangpu Avenue West, Guangzhou, China.
Department of Cardiology, the First Affiliated Hospital of Jinan University, Guangzhou, China.
Biochem Pharmacol. 2020 Aug;178:114045. doi: 10.1016/j.bcp.2020.114045. Epub 2020 May 22.
Dosing time accounts for a large variability in efficacy and/or toxicity for many drugs. Therefore, chronotherapy has been shown to effectively improve drug efficacy and to reduce drug toxicity. Circadian changes in pharmacokinetics and pharmacodynamics (drug target) are two essential sources of time-varying drug effects. Pharmacokinetics determines the drug and metabolite concentrations (exposure) in target tissues/organs, thereby impacting drug efficacy and toxicity. Pharmacokinetic processes are generally divided into drug absorption, distribution, metabolism and excretion (so-called "ADME"). Recent years of studies have revealed circadian (~24 h) rhythms in ADME processes, and clarified the underlying mechanisms related to circadian clock regulation. Furthermore, there is accumulating evidence that circadian pharmacokinetics can be translated to chronotoxicity and chronoefficacy. In this article, we review circadian rhythms in pharmacokinetic behaviors along with the underlying mechanisms. We also discuss the correlations of circadian pharmacokinetics with chronotoxicity and chronoefficacy.
许多药物的疗效和/或毒性在很大程度上受给药时间的影响。因此,时间治疗已被证明可以有效地提高药物疗效,降低药物毒性。药代动力学和药效学(药物靶点)的昼夜节律变化是药物时变效应的两个重要来源。药代动力学决定了药物和代谢物在靶组织/器官中的浓度(暴露),从而影响药物的疗效和毒性。药代动力学过程通常分为药物吸收、分布、代谢和排泄(所谓的“ADME”)。近年来的研究揭示了 ADME 过程中的昼夜节律(~24 小时),并阐明了与昼夜节律调节相关的潜在机制。此外,越来越多的证据表明,昼夜药代动力学可以转化为时间毒性和时间疗效。本文综述了药代动力学行为的昼夜节律及其潜在机制。我们还讨论了昼夜药代动力学与时间毒性和时间疗效的相关性。