Time-restricted feeding modulates gene expression related with rhythm and inflammation in Mongolian gerbils

IF 3.9 3区 环境科学与生态学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology C-toxicology & Pharmacology Pub Date : 2024-09-10 DOI:10.1016/j.cbpc.2024.110038
Lin Yang , Xi-Zhi Wang , Chen-Zhu Wang , De-Hua Wang , Zhen-Shan Wang , Xue-Ying Zhang
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Abstract

Time-restricted feeding (TRF) has the potential to modulate circadian rhythm and widely studied in humans and laboratory mice. However, less is known about the physiological responses to TRF in wild mammals. Here, we used Mongolian gerbils, Meriones unguiculatus, to explore the effect of 6-week TRF on gene expression related with circadian rhythm and inflammation. The TRF gerbils had higher cumulative food intake than the ad libitum (AL) group, but body mass, feeding frequency/time and metabolic rate did not differ between groups. In the hypothalamus, downregulation of rhythm-related genes Per3, Cry1 and Dbp was detected in the daytime-restricted feeding (DRF) group and Cry1 was downregulated in the nighttime-restricted feeding (NRF) group. In the liver, the expression of Per1/3, Rev-erbα/β and Dbp was lower, and Bmal1 was higher in the DRF than in AL group, while NRF gerbils showed no changes. In the colon, the expression of Bmal1 and Cry1 was higher but Per3, Rev-erbα/β and Dbp were lower in the DRF than in AL group. Further, the expression of inflammation-related genes such as NF-κB, IL-1β, IL-18 and Nlrp3 was lower in the liver of DRF gerbils, and IL-1β was lower both in the hypothalamus and liver of NRF gerbils. Moreover, the genes related with inflammation such as NF-κB, Nlrp3, IL-10/18/1β and Tnf-α were positively or negatively correlated with multiple rhythm-related genes in the central and peripheral organs. In conclusion, TRF, particularly DRF, could modulate rhythm-related genes in the central and peripheral tissues and reduce hepatic expression of inflammation-related genes in gerbils.

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限时喂养可调节蒙古沙鼠体内与节律和炎症有关的基因表达。
限时喂食(TRF)具有调节昼夜节律的潜力,并在人类和实验鼠身上得到广泛研究。然而,人们对野生哺乳动物对TRF的生理反应知之甚少。在这里,我们用蒙古沙鼠(Meriones unguiculatus)来探讨为期6周的TRF对昼夜节律和炎症相关基因表达的影响。与自由采食组相比,TRF组沙鼠的累积食物摄入量更高,但体重、采食频率/时间和代谢率在组间没有差异。在下丘脑中,日间限食(DRF)组发现昼夜节律基因Per3、Cry1和Dbp表达下调,而夜间限食(NRF)组发现Cry1表达下调。在肝脏中,DRF组Per1/3、Rev-erbα/β和Dbp的表达量低于AL组,Bmal1的表达量高于AL组,而NRF组沙鼠的表达量没有变化。在结肠中,DRF组的Bmal1和Cry1表达量高于AL组,但Per3、Rev-erbα/β和Dbp的表达量低于AL组。此外,炎症相关基因如NF-κB、IL-1β、IL-18和Nlrp3在DRF组沙鼠肝脏中的表达量较低,而IL-1β在NRF组沙鼠下丘脑和肝脏中的表达量均较低。此外,NF-κB、Nlrp3、IL-10/18/1β和Tnf-α等炎症相关基因与中枢和外周器官的多个节律相关基因呈正或负相关。总之,TRF(尤其是DRF)可以调节中枢和外周组织中的节律相关基因,减少沙鼠肝脏炎症相关基因的表达。
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来源期刊
CiteScore
7.50
自引率
5.10%
发文量
206
审稿时长
30 days
期刊介绍: Part C: Toxicology and Pharmacology. This journal is concerned with chemical and drug action at different levels of organization, biotransformation of xenobiotics, mechanisms of toxicity, including reactive oxygen species and carcinogenesis, endocrine disruptors, natural products chemistry, and signal transduction with a molecular approach to these fields.
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