Circadian rhythms: influence on physiology, pharmacology, and therapeutic interventions

被引:88
作者
Ayyar, Vivaswath S. [1 ,2 ]
Sukumaran, Siddharth [1 ,2 ]
机构
[1] SUNY Buffalo, Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Buffalo, NY 14214 USA
[2] Pharmaceut Companies Johnson & Johnson, Janssen, Spring House, PA 19477 USA
关键词
Circadian rhythms; Chronobiology; Molecular clock; Drug disposition; Pharmacodynamics; Chronotherapeutics; Systems pharmacology;
D O I
10.1007/s10928-021-09751-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Circadian rhythms are ubiquitous phenomena that recur daily in a self-sustaining, entrainable, and oscillatory manner, and orchestrate a wide range of molecular, physiological, and behavioral processes. Circadian clocks are comprised of a hierarchical network of central and peripheral clocks that generate, sustain, and synchronize the circadian rhythms. The functioning of the peripheral clock is regulated by signals from autonomic innervation (from the central clock), endocrine networks, feeding, and other external cues. The critical role played by circadian rhythms in maintaining both systemic and tissue-level homeostasis is well established, and disruption of the rhythm has direct consequence for human health, disorders, and diseases. Circadian oscillations in both pharmacokinetics and pharmacodynamic processes are known to affect efficacy and toxicity of several therapeutic agents. A variety of modeling approaches ranging from empirical to more complex systems modeling approaches have been applied to characterize circadian biology and its influence on drug actions, optimize time of dosing, and identify opportunities for pharmacological modulation of the clock mechanisms and their downstream effects. In this review, we summarize current understanding of circadian rhythms and its influence on physiology, pharmacology, and therapeutic interventions, and discuss the role of chronopharmacometrics in gaining new insights into circadian rhythms and its applications in chronopharmacology.
引用
收藏
页码:321 / 338
页数:18
相关论文
共 142 条
[2]   Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus [J].
Akhtar, RA ;
Reddy, AB ;
Maywood, ES ;
Clayton, JD ;
King, VM ;
Smith, AG ;
Gant, TW ;
Hastings, MH ;
Kyriacou, CP .
CURRENT BIOLOGY, 2002, 12 (07) :540-550
[3]   CIRCADIAN METABOLIC PATTERNS IN CULTURED HAMSTER ADRENAL GLANDS [J].
ANDREWS, RV ;
FOLK, GE .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY, 1964, 11 (04) :393-&
[4]  
ANGELI A, 1978, CLIN PHARMACOL THER, V23, P47
[5]  
Antoch Marina P, 2013, Handb Exp Pharmacol, P289, DOI 10.1007/978-3-642-25950-0_12
[6]  
Aulinas A, PHYSL PINEAL GLAND M
[7]   Transitioning from Basic toward Systems Pharmacodynamic Models: Lessons from Corticosteroids [J].
Ayyar, Vivaswath S. ;
Jusko, William J. .
PHARMACOLOGICAL REVIEWS, 2020, 72 (02) :414-438
[8]   Modeling Corticosteroid Pharmacokinetics and Pharmacodynamics, Part III: Estrous Cycle and Estrogen Receptor-Dependent Antagonism of Glucocorticoid-Induced Leucine Zipper (GILZ) Enhancement by Corticosteroids [J].
Ayyar, Vivaswath S. ;
DuBois, Debra C. ;
Almo, Richard R. ;
Jusko, William J. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2019, 370 (02) :337-349
[9]   Indirect pharmacodynamic models for responses with circadian removal [J].
Ayyar, Vivaswath S. ;
Krzyzanski, Wojciech ;
Jusko, William J. .
JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2019, 46 (01) :89-101
[10]   Mechanistic Multi-Tissue Modeling of Glucocorticoid-Induced Leucine Zipper Regulation: Integrating Circadian Gene Expression with Receptor-Mediated Corticosteroid Pharmacodynamics [J].
Ayyar, Vivaswath S. ;
DuBois, Debra C. ;
Almon, Richard R. ;
Jusko, William J. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2017, 363 (01) :45-57