Nuclear Receptors Linking Circadian Rhythms and Cardiometabolic Control

被引:52
作者
Duez, Helene [1 ]
Staels, Bart
机构
[1] Inst Pasteur, INSERM, UR1011, F-59019 Lille, France
关键词
circadian rhythm; cardiometabolic disorders; nuclear receptors; Rev-erb alpha ROR alpha PPAR; PGC1; alpha; biological clock; metabolic syndrome; diabetes mellitus; gene expression; insulin resistance; metabolism; REV-ERB-ALPHA; CLOCK GENE-EXPRESSION; METABOLIC SYNDROME; BLOOD-PRESSURE; TARGET GENE; PERIPHERAL-TISSUES; STAGGERER MOUSE; SHIFT WORK; ROR-ALPHA; OBESITY;
D O I
10.1161/ATVBAHA.110.209098
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Many behavioral and physiological processes, including locomotor activity, blood pressure, body temperature, sleep (fasting)/wake (feeding) cycles, and metabolic regulation display diurnal rhythms. The biological clock ensures proper metabolic alignment of energy substrate availability and processing. Studies in animals and humans highlight a strong link between circadian disorders and altered metabolic responses and cardiovascular events. Shift work, for instance, increases the risk to develop metabolic abnormalities resembling the metabolic syndrome. Nuclear receptors have long been known as metabolic regulators. Several of them (ie, Rev-erb alpha, ROR alpha, and peroxisome proliferation activated receptors) are subjected to circadian variations and are integral components of molecular clock machinery. In turn, these nuclear receptors regulate downstream target genes in a circadian manner, acting to properly gate metabolic events to the appropriate circadian time window. (Arterioscler Thromb Vasc Biol. 2010;30:1529-1534.)
引用
收藏
页码:1529 / 1534
页数:6
相关论文
共 74 条
[1]   Rhythmic messenger ribonucleic acid expression of clock genes and adipocytokines in mouse visceral adipose tissue [J].
Ando, H ;
Yanagihara, H ;
Hayashi, Y ;
Obi, Y ;
Tsuruoka, S ;
Takamura, T ;
Kaneko, S ;
Fujimura, A .
ENDOCRINOLOGY, 2005, 146 (12) :5631-5636
[2]   Vascular Disease in Mice With a Dysfunctional Circadian Clock [J].
Anea, Ciprian B. ;
Zhang, Maoxiang ;
Stepp, David W. ;
Simkins, G. Bryan ;
Reed, Guy ;
Fulton, David J. ;
Rudic, R. Daniel .
CIRCULATION, 2009, 119 (11) :1510-U88
[3]   Elovl3:: a model gene to dissect homeostatic links between the circadian clock and nutritional status [J].
Anzulovich, Ana ;
Mir, Alain ;
Brewer, Michelle ;
Ferreyra, Gabriela ;
Vinson, Charles ;
Baler, Ruben .
JOURNAL OF LIPID RESEARCH, 2006, 47 (12) :2690-2700
[4]   SIRT1 regulates circadian clock gene expression through PER2 deacetylation [J].
Asher, Gad ;
Gatfield, David ;
Stratmann, Markus ;
Reinke, Hans ;
Dibner, Charna ;
Kreppel, Florian ;
Mostoslavsky, Raul ;
Alt, Frederick W. ;
Schibler, Ueli .
CELL, 2008, 134 (02) :317-328
[5]   Resetting of circadian time peripheral tissues by glucocorticoid signaling [J].
Balsalobre, A ;
Brown, SA ;
Marcacci, L ;
Tronche, F ;
Kellendonk, C ;
Reichardt, HM ;
Schütz, G ;
Schibler, U .
SCIENCE, 2000, 289 (5488) :2344-2347
[6]   Smooth muscle dysfunction in resistance arteries of the staggerer mouse, a mutant of the nuclear receptor RORα [J].
Besnard, S ;
Bakouche, J ;
Lemaigre-Dubreuil, Y ;
Mariani, J ;
Tedgui, A ;
Henrion, D .
CIRCULATION RESEARCH, 2002, 90 (07) :820-825
[7]   Disruption of circadian insulin secretion is associated with reduced glucose uptake in first-degree relatives of patients with type 2 diabetes [J].
Boden, G ;
Chen, XH ;
Polansky, M .
DIABETES, 1999, 48 (11) :2182-2188
[8]   Disruption of the circadian clock within the cardiomyocyte influences myocardial contractile function, metabolism, and gene expression [J].
Bray, Molly S. ;
Shaw, Chad A. ;
Moore, Michael W. S. ;
Garcia, Rodrigo A. P. ;
Zanquetta, Melissa M. ;
Durgan, David J. ;
Jeong, William J. ;
Tsai, Ju-Yun ;
Bugger, Heiko ;
Zhang, Dongfang ;
Rohrwasser, Andreas ;
Rennison, Julie H. ;
Dyck, Jason R. B. ;
Litwin, Sheldon E. ;
Hardin, Paul E. ;
Chow, Chi-Wing ;
Chandler, Margaret P. ;
Abel, E. Dale ;
Young, Martin E. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2008, 294 (02) :H1036-H1047
[9]   Restoration of adiponectin pulsatility in severely obese subjects after weight loss [J].
Calvani, M ;
Scarfone, A ;
Granato, L ;
Mora, EV ;
Nanni, G ;
Castagneto, M ;
Greco, AV ;
Manco, M ;
Mingrone, G .
DIABETES, 2004, 53 (04) :939-947
[10]   Hemodynamic effects of fenofibrate and coenzyme Q10 in type 2 diabetic subjects with left ventricular diastolic dysfunction [J].
Chew, Gerard T. ;
Watts, Gerald F. ;
Davis, Timothy M. E. ;
Stuckey, Bronwyn G. A. ;
Beilin, Lawrence J. ;
Thompson, Peter L. ;
Burke, Valerie ;
Currie, Philip J. .
DIABETES CARE, 2008, 31 (08) :1502-1509