Potential mechanism of hepatic lipid accumulation during a long-term rest phase restricted feeding in mice

被引:4
作者
Tsurudome, Yuya [1 ]
Akamine, Takahiro [2 ]
Horiguchi, Michiko [1 ]
Wada, Yukiyo [1 ]
Fujimura, Akio [1 ,3 ]
Ushijima, Kentaro [1 ,3 ]
机构
[1] Sanyo Onoda City Univ, Fac Pharmaceut Sci, Div Pharmaceut, Yamaguchi 7560884, Japan
[2] Oita Univ, Fac Med, Dept Pharmacol, Oita, Japan
[3] Jichi Med Univ, Dept Pharmacol, Div Clin Pharmacol, Shimotsuke, Tochigi, Japan
关键词
Restricted feeding; hepatic lipid accumulation; miR-27b-3p; PPAR gamma; CD36; NIGHT-SHIFT WORK; ENERGY-METABOLISM; CIRCADIAN-RHYTHMS; PPAR-GAMMA; EXPRESSION; LIVER; TIME; TRANSCRIPTION; CLOCK; LEVEL;
D O I
10.1080/07420528.2022.2077746
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Eating during a rest phase disrupts the biological clock system and leads to obesity and metabolic diseases. Although a rest phase restricted feeding (RF) is reported to enhance hepatic lipid accumulation, the mechanism(s) of the phenomenon is still unknown. This study evaluated the potential involvement of the CD36-related transport of lipids into the liver in mice with the RF procedure. This study showed that hepatic lipid accumulation was more significant in the RF group compared with mice under an active phase restricted feeding (AF). The RF procedure also elevated the expression of CD36 mRNA and its protein on the cellular membrane throughout the day. The transcription factor profiling array revealed that the RF activated the proliferator-activated receptor-gamma (PPAR gamma), one of the CD36 transcript enhancers. In the liver of RF mice, the expression of miR-27b-3p, which is known to interfere with PPAR gamma gene expression, significantly decreased. These results suggest that the RF procedure inhibits the expression of miR-27b-3p in the liver and subsequently elevates PPAR gamma activity. Activated PPAR gamma might lead to CD36 upregulation, which, in turn, stimulates the transport of lipids into the liver.
引用
收藏
页码:1132 / 1143
页数:12
相关论文
共 34 条
[1]   Circadian Timing of Food Intake Contributes to Weight Gain [J].
Arble, Deanna M. ;
Bass, Joseph ;
Laposky, Aaron D. ;
Vitaterna, Martha H. ;
Turek, Fred W. .
OBESITY, 2009, 17 (11) :2100-2102
[2]   Crosstalk between Components of Circadian and Metabolic Cycles in Mammals [J].
Asher, Gad ;
Schibler, Ueli .
CELL METABOLISM, 2011, 13 (02) :125-137
[3]   CIRCADIAN-RHYTHM IN HEPATIC LOW-DENSITY-LIPOPROTEIN (LDL)-RECEPTOR EXPRESSION AND PLASMA LDL LEVELS [J].
BALASUBRAMANIAM, S ;
SZANTO, A ;
ROACH, PD .
BIOCHEMICAL JOURNAL, 1994, 298 :39-43
[4]   Circadian Integration of Metabolism and Energetics [J].
Bass, Joseph ;
Takahashi, Joseph S. .
SCIENCE, 2010, 330 (6009) :1349-1354
[5]   Quantitative analysis of light-phase restricted feeding reveals metabolic dyssynchrony in mice [J].
Bray, M. S. ;
Ratcliffe, W. F. ;
Grenett, M. H. ;
Brewer, R. A. ;
Gamble, K. L. ;
Young, M. E. .
INTERNATIONAL JOURNAL OF OBESITY, 2013, 37 (06) :843-852
[6]   microRNA-155 promotes the proliferation of prostate cancer cells by targeting annexin 7 [J].
Cai, Zhi-Kang ;
Chen, Qi ;
Chen, Yan-Bo ;
Gu, Meng ;
Zheng, Da-Chao ;
Zhou, Juan ;
Wang, Zhong .
MOLECULAR MEDICINE REPORTS, 2015, 11 (01) :533-538
[7]   Omega-3 Fatty Acids and Inflammatory Processes [J].
Calder, Philip C. .
NUTRIENTS, 2010, 2 (03) :355-374
[8]   Predicted MicroRNAs for Mammalian Circadian Rhythms [J].
Figueredo, Diego de Siqueira ;
Barbosa, Mayara Rodrigues ;
Goes Gitai, Daniel Leite ;
de Andrade, Tiago Gomes .
JOURNAL OF BIOLOGICAL RHYTHMS, 2013, 28 (02) :107-116
[9]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[10]   Metabolism and Circadian Rhythms-Implications for Obesity [J].
Froy, Oren .
ENDOCRINE REVIEWS, 2010, 31 (01) :1-24