Acrylamide Defects the Expression Pattern of the Circadian Clock and Mitochondria! Dynamics in C57BL/6J Mice Liver and HepG2 Cells

被引:22
作者
Tan, Xintong [1 ]
Zhao, Tong [1 ]
Wang, Zihan [1 ]
Wang, Jia [1 ]
Wang, Yijie [1 ]
Liu, Zhigang [1 ]
Liu, Xuebo [1 ]
机构
[1] Northwest A&F Univ, Coll Food Sci & Engn, Lab Funct Chem & Nutr Food, Xinong Rd 2, Yangling 712100, Shaanxi, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
acrylamide; liver; circadian clock; mitochondrial dynamic; redox status; OXIDATIVE STRESS; DIETARY ACRYLAMIDE; REV-ERB; BMAL1; TRANSCRIPTION; EXPOSURE; ARCHITECTURE; PHYSIOLOGY; COMPONENT; APOPTOSIS;
D O I
10.1021/acs.jafc.8b02473
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Circadian rhythm helps organisms adapt to their environment and control a variety of physiological and metabolic processes. Acrylamide is a toxic compound that can be produced during food processing. The aim of this research is to investigate whether the circadian clock is involved in the toxicity mechanisms of acrylamide in mice liver. Our results revealed that acrylamide markedly induced circadian gene oscillation disorder and blocked circadian-related protein in mice liver and HepG2 cells. Simultaneously, the balance of the daily oscillation of the antioxidant enzymes was impeded under acrylamide treatment. Furthermore, acrylamide treatment elevated the mitochondrial dynamic gene expressions and influenced the mitochondrial morphology at the night phase. Acrylamide blocked circadian protein expression via repressing the phosphorylation of AKT or inducing oxidative stress. Taken together, our work reveals acrylamide as a clock-repressing compound generated through the Maillard browning reaction in certain foods that may possess a toxic effect via circadian clock mechanisms.
引用
收藏
页码:10252 / 10266
页数:15
相关论文
共 59 条
[1]  
DEVRIES N, 1993, J CELL BIOCHEM, P270
[2]   Clocks, Metabolism, and the Epigenome [J].
Feng, Dan ;
Lazar, Mitchell A. .
MOLECULAR CELL, 2012, 47 (02) :158-167
[3]   Chronic Ethanol Consumption Disrupts the Core Molecular Clock and Diurnal Rhythms of Metabolic Genes in the Liver without Affecting the Suprachiasmatic Nucleus [J].
Filiano, Ashley N. ;
Millender-Swain, Telisha ;
Johnson, Russell, Jr. ;
Young, Martin E. ;
Gamble, Karen L. ;
Bailey, Shannon M. .
PLOS ONE, 2013, 8 (08)
[4]   Chemistry, biochemistry, and safety of acrylamide. A review [J].
Friedman, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (16) :4504-4526
[5]   The circadian gene Period2 plays an important role in tumor suppression and DNA damage response in vivo [J].
Fu, LN ;
Pelicano, H ;
Liu, JS ;
Huang, P ;
Lee, CC .
CELL, 2002, 111 (01) :41-50
[6]   The circadian PAR-domain basic leucine zipper transcription factors DBP, TEF, and HLF modulate basal and inducible xenobiotic detoxification [J].
Gachon, Federic ;
Olela, Fabienne Fleury ;
Schaad, Olivier ;
Descombes, Patrick ;
Schibler, Ueli .
CELL METABOLISM, 2006, 4 (01) :25-36
[7]  
Gawel Stefan, 2004, Wiad Lek, V57, P453
[8]   Biomarker monitoring of controlled dietary acrylamide exposure indicates consistent human endogenous background [J].
Goempel, Katharina ;
Tedsen, Laura ;
Ruenz, Meike ;
Bakuradze, Tamara ;
Schipp, Dorothea ;
Galan, Jens ;
Eisenbrand, Gerhard ;
Richling, Elke .
ARCHIVES OF TOXICOLOGY, 2017, 91 (11) :3551-3560
[9]   Role of cytochromes P450 in chemical toxicity and oxidative stress: studies with CYP2E1 [J].
Gonzalez, FJ .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 569 (1-2) :101-110
[10]   The circadian clock component BMAL1 is a critical regulator of p21WAF1/CIP1 expression and hepatocyte proliferation [J].
Grechez-Cassiau, Aline ;
Rayet, Beatrice ;
Guillaumond, Fabienne ;
Teboul, Michele ;
Delaunay, Franck .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (08) :4535-4542