Yang Lin, Wang Xi-Zhi, Wang Chen-Zhu, Wang De-Hua, Wang Zhen-Shan, Zhang Xue-Ying
School of Life Sciences, Hebei University, Baoding 071002, China; State Key Laboratory of Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
State Key Laboratory of Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Comp Biochem Physiol C Toxicol Pharmacol. 2025 Jan;287:110038. doi: 10.1016/j.cbpc.2024.110038. Epub 2024 Sep 10.
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.
限时进食(TRF)有调节昼夜节律的潜力,并且在人类和实验室小鼠中得到了广泛研究。然而,对于野生哺乳动物对TRF的生理反应了解较少。在此,我们使用长爪沙鼠(Meriones unguiculatus)来探究6周的TRF对与昼夜节律和炎症相关的基因表达的影响。TRF组沙鼠的累积食物摄入量高于自由进食(AL)组,但两组之间的体重、进食频率/时间和代谢率并无差异。在下丘脑,白天限时进食(DRF)组中与节律相关的基因Per3、Cry1和Dbp表达下调,夜间限时进食(NRF)组中Cry1表达下调。在肝脏中,DRF组中Per1/3、Rev-erbα/β和Dbp的表达较低,而Bmal1的表达高于AL组,而NRF组沙鼠则无变化。在结肠中,DRF组中Bmal1和Cry1的表达较高,但Per3、Rev-erbα/β和Dbp的表达低于AL组。此外,DRF组沙鼠肝脏中炎症相关基因如NF-κB、IL-1β、IL-18和Nlrp3的表达较低,NRF组沙鼠下丘脑和肝脏中的IL-1β均较低。此外,在中枢和外周器官中,NF-κB、Nlrp3、IL-10/18/1β和Tnf-α等与炎症相关的基因与多个节律相关基因呈正相关或负相关。总之,TRF,尤其是DRF,可以调节中枢和外周组织中与节律相关的基因,并降低沙鼠肝脏中炎症相关基因的表达。