Comparative Circadian Metabolomics Reveal Differential Effects of Nutritional Challenge in the Serum and Liver

被引:51
作者
Abbondante, Serena [1 ,2 ]
Eckel-Mahan, Kristin L. [1 ,2 ]
Ceglia, Nicholas J. [2 ,3 ]
Baldi, Pierre [2 ,3 ]
Sassone-Corsi, Paolo [1 ,2 ]
机构
[1] Univ Calif Irvine, INSERM, Ctr Epigenet & Metab, U904, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Sch Informat & Comp Sci, Inst Genom & Bioinformat, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
CARDIOVASCULAR RISK-FACTORS; BODY-MASS INDEX; SHIFT WORK; ADIPOSE-TISSUE; INSULIN SENSITIVITY; BETA-SITOSTEROL; KEY PATHWAYS; METABOLISM; CLOCK; OBESITY;
D O I
10.1074/jbc.M115.681130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diagnosis and therapeutic interventions in pathological conditions rely upon clinical monitoring of key metabolites in the serum. Recent studies show that a wide range of metabolic pathways are controlled by circadian rhythms whose oscillation is affected by nutritional challenges, underscoring the importance of assessing a temporal window for clinical testing and thereby questioning the accuracy of the reading of critical pathological markers in circulation. We have been interested in studying the communication between peripheral tissues under metabolic homeostasis perturbation. Here we present a comparative circadian metabolomic analysis on serum and liver in mice under high fat diet. Our data reveal that the nutritional challenge induces a loss of serum metabolite rhythmicity compared with liver, indicating a circadian misalignment between the tissues analyzed. Importantly, our results show that the levels of serum metabolites do not reflect the circadian liver metabolic signature or the effect of nutritional challenge. This notion reveals the possibility that misleading reads of metabolites in circulation may result in misdiagnosis and improper treatments. Our findings also demonstrate a tissue-specific and time-dependent disruption of metabolic homeostasis in response to altered nutrition.
引用
收藏
页码:2812 / 2828
页数:17
相关论文
共 106 条
[1]   Circadian Clocks and Feeding Time Regulate the Oscillations and Levels of Hepatic Triglycerides [J].
Adamovich, Yaarit ;
Rousso-Noori, Liat ;
Zwighaft, Ziv ;
Neufeld-Cohen, Adi ;
Golik, Marina ;
Kraut-Cohen, Judith ;
Wang, Miao ;
Han, Xianlin ;
Asher, Gad .
CELL METABOLISM, 2014, 19 (02) :319-330
[2]   Obesity and shift work: chronobiological aspects [J].
Antunes, L. C. ;
Levandovski, R. ;
Dantas, G. ;
Caumo, W. ;
Hidalgo, M. P. .
NUTRITION RESEARCH REVIEWS, 2010, 23 (01) :155-168
[3]   Correlation of shift work and waist circumference, body mass index, chronotype and depressive symptoms [J].
Antunes, Luciana da Conceicao ;
da Jornada, Manoela Neves ;
Ramalho, Leticia ;
Loayza Hidalgo, Maria Paz .
ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA, 2010, 54 (07) :652-656
[4]   Time for Food: The Intimate Interplay between Nutrition, Metabolism, and the Circadian Clock [J].
Asher, Gad ;
Sassone-Corsi, Paolo .
CELL, 2015, 161 (01) :84-92
[5]   Chemopreventive potential of β-Sitosterol in experimental colon cancer model - an In vitro and In vivo study [J].
Baskar, Albert A. ;
Ignacimuthu, Savarimuthu ;
Paulraj, Gabriel M. ;
Al Numair, Khalid S. .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2010, 10
[6]   Circadian topology of metabolism [J].
Bass, Joseph .
NATURE, 2012, 491 (7424) :348-356
[7]   SIRT1 is a circadian deacetylase for core clock components [J].
Belden, William J. ;
Dunlap, Jay C. .
CELL, 2008, 134 (02) :212-214
[8]   Metabolism addiction in pancreatic cancer [J].
Blum, R. ;
Kloog, Y. .
CELL DEATH & DISEASE, 2014, 5 :e1065-e1065
[9]   Purine salvage to adenine nucleotides in different skeletal muscle fiber types [J].
Brault, JJ ;
Terjung, RL .
JOURNAL OF APPLIED PHYSIOLOGY, 2001, 91 (01) :231-238
[10]   Genome-wide expression analysis in Drosophila reveals genes controlling circadian behavior [J].
Ceriani, MF ;
Hogenesch, JB ;
Yanovsky, M ;
Panda, S ;
Straume, M ;
Kay, SA .
JOURNAL OF NEUROSCIENCE, 2002, 22 (21) :9305-9319