Circadian Metabolism in the Light of Evolution

被引:129
作者
Gerhart-Hines, Zachary [1 ,4 ]
Lazar, Mitchell A. [2 ,3 ,5 ]
机构
[1] Univ Copenhagen, Novo Nordisk Fdn, Ctr Basic Metab Res, Sect Metab Receptol, DK-2200 Copenhagen N, Denmark
[2] Univ Penn, Dept Genet, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[4] Univ Copenhagen, Blegdamsvej 3b,18-5-52, DK-2200 Copenhagen N, Denmark
[5] Univ Penn, Smilow Ctr Translat Res 12 102, 3400 Civic Ctr Blvd, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院; 欧洲研究理事会;
关键词
REV-ERB-ALPHA; BROWN ADIPOSE-TISSUE; CLOCK TRANSCRIPTION FACTOR; GENE-EXPRESSION; SKELETAL-MUSCLE; BLOOD-PRESSURE; SHIFT WORK; MYOCARDIAL-METABOLISM; MAMMALIAN CLOCK; CONTRACTILE FUNCTION;
D O I
10.1210/er.2015-1007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Circadian rhythm, or daily oscillation, of behaviors and biological processes is a fundamental feature of mammalian physiology that has developed over hundreds of thousands of years under the continuous evolutionary pressure of energy conservation and efficiency. Evolution has fine-tuned the body's clock to anticipate and respond to numerous environmental cues in order to maintain homeostatic balance and promote survival. However, we now live in a society in which these classic circadian entrainment stimuli have been dramatically altered from the conditions under which the clock machinery was originally set. A bombardment of artificial lighting, heating, and cooling systems that maintain constant ambient temperature; sedentary lifestyle; and the availability of inexpensive, high-calorie foods has threatened even the most powerful and ancient circadian programming mechanisms. Such environmental changes have contributed to the recent staggering elevation in lifestyle-influenced pathologies, including cancer, cardiovascular disease, depression, obesity, and diabetes. This review scrutinizes the role of the body's internal clocks in the hard-wiring of circadian networks that have evolved to achieve energetic balance and adaptability, and it discusses potential therapeutic strategies to reset clock metabolic control to modern time for the benefit of human health.
引用
收藏
页码:289 / 304
页数:16
相关论文
共 210 条
[81]   THE CIRCADIAN CHANGE OF GLUCONEOGENESIS IN THE LIVER INVIVO IN FED RATS [J].
KIDA, K ;
NISHIO, T ;
YOKOZAWA, T ;
NAGAI, K ;
MATSUDA, H ;
NAKAGAWA, H .
JOURNAL OF BIOCHEMISTRY, 1980, 88 (04) :1009-1013
[82]   Positional cloning of the mouse circadian Clock gene [J].
King, DP ;
Zhao, YL ;
Sangoram, AM ;
Wilsbacher, LD ;
Tanaka, M ;
Antoch, MP ;
Steeves, TDL ;
Vitaterna, MH ;
Kornhauser, JM ;
Lowrey, PL ;
Turek, FW ;
Takahashi, JS .
CELL, 1997, 89 (04) :641-653
[83]   The Drosophila clock gene double-time encodes a protein closely related to human casein kinase Iε [J].
Kloss, B ;
Price, JL ;
Saez, L ;
Blau, J ;
Rothenfluh, A ;
Wesley, CS ;
Young, MW .
CELL, 1998, 94 (01) :97-107
[84]   Molecular components of the mammalian circadian clock [J].
Ko, Caroline H. ;
Takahashi, Joseph S. .
HUMAN MOLECULAR GENETICS, 2006, 15 :R271-R277
[85]   Characterization of photolyase/blue-light receptor homologs in mouse and human cells [J].
Kobayashi, K ;
Kanno, S ;
Smit, R ;
van der Horst, GTJ ;
Takao, M ;
Yasui, A .
NUCLEIC ACIDS RESEARCH, 1998, 26 (22) :5086-5092
[86]   High-fat diet disrupts behavioral and molecular circadian rhythms in mice [J].
Kohsaka, Akira ;
Laposky, Aaron D. ;
Ramsey, Kathryn Moynihan ;
Estrada, Carmela ;
Joshu, Corinne ;
Kobayashi, Yurniko ;
Turek, Fred W. ;
Bass, Joseph .
CELL METABOLISM, 2007, 6 (05) :414-421
[87]   Transcriptional Architecture and Chromatin Landscape of the Core Circadian Clock in Mammals [J].
Koike, Nobuya ;
Yoo, Seung-Hee ;
Huang, Hung-Chung ;
Kumar, Vivek ;
Lee, Choogon ;
Kim, Tae-Kyung ;
Takahashi, Joseph S. .
SCIENCE, 2012, 338 (6105) :349-354
[88]   CLOCK MUTANTS OF DROSOPHILA-MELANOGASTER [J].
KONOPKA, RJ ;
BENZER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1971, 68 (09) :2112-+
[89]   Work characteristics and incidence of type 2 diabetes in women [J].
Kroenke, Candyce H. ;
Spiegelman, Donna ;
Manson, Joann ;
Schernhammer, Eva S. ;
Colditz, Graham A. ;
Kawachi, Ichiro .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2007, 165 (02) :175-183
[90]   Night-time restricted feeding normalises clock genes and Pai-1 gene expression in the db/db mouse liver [J].
Kudo, T ;
Akiyama, M ;
Kuriyama, K ;
Sudo, M ;
Moriya, T ;
Shibata, S .
DIABETOLOGIA, 2004, 47 (08) :1425-1436