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配种前母体间歇性禁食可改变后代肝脏的 DNA 甲基化。

Maternal intermittent fasting before mating alters hepatic DNA methylation in offspring.

机构信息

Department of Physiology & Pathophysiology, Peking University Health Science Center, Beijing 100191, China.

出版信息

Epigenomics. 2021 Mar;13(5):341-356. doi: 10.2217/epi-2020-0403. Epub 2021 Jan 28.

Abstract

Our aim was to explore how maternal intermittent fasting (IF) influences offspring metabolism. A model of female C57BL/6J mice alternate-day feeding before mating was established and alteration of hepatic DNA methylation in offspring analyzed by whole genome bisulfite sequencing. IF dams weighed less (p = 0.03) and had lower random blood glucose levels (p = 0.04). Lower birth weight (p = 0.0031) and impaired glucose metabolism were also observed in the offspring of the IF mice. The hepatic genome-wide DNA methylation maps showed a correlation between maternal IF and decreased hepatic global DNA methylation of adult offspring. In the offspring liver, 2869 differentially methylated DNA regions were altered. Our finding suggests that maternal IF before mating significantly alters hepatic DNA methylation in offspring.

摘要

我们的目的是探讨母体间歇性禁食(IF)如何影响后代的新陈代谢。建立了雌性 C57BL/6J 小鼠在交配前隔日喂养的模型,并通过全基因组亚硫酸氢盐测序分析了后代肝 DNA 甲基化的改变。IF 组母鼠体重较轻(p=0.03),随机血糖水平较低(p=0.04)。IF 组小鼠的后代出生体重也较低(p=0.0031),葡萄糖代谢受损。肝基因组全范围 DNA 甲基化图谱显示,母体 IF 与成年后代肝内整体 DNA 甲基化减少之间存在相关性。在后代肝脏中,有 2869 个差异甲基化 DNA 区域发生改变。我们的研究结果表明,交配前母体 IF 可显著改变后代肝脏的 DNA 甲基化。

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