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妊娠时差会导致晚年骨骼和心脏疾病。

Gestational jet lag predisposes to later-life skeletal and cardiac disease.

机构信息

a Department of Molecular Genetics , University Medical Center Rotterdam , Rotterdam , The Netherlands.

b Department of Internal Medicine , University Medical Center Rotterdam , Rotterdam , The Netherlands.

出版信息

Chronobiol Int. 2019 May;36(5):657-671. doi: 10.1080/07420528.2019.1579734. Epub 2019 Feb 22.

Abstract

Circadian rhythm disturbance (CRD) increases the risk of disease, e.g. metabolic syndrome, cardiovascular disease, and cancer. In the present study, we investigated later life adverse health effects triggered by repeated jet lag during gestation. Pregnant mice were subjected to a regular light-dark cycle (CTRL) or to a repeated delay (DEL) or advance (ADV) jet lag protocol. Both DEL and ADV offspring showed reduced weight gain. ADV offspring had an increased circadian period, and an altered response to a jet lag was observed in both DEL and ADV offspring. Analysis of the bones of adult male ADV offspring revealed reduced cortical bone mass and strength. Strikingly, analysis of the heart identified structural abnormalities and impaired heart function. Finally, DNA methylation analysis revealed hypermethylation of miR17-92 cluster and differential methylation within circadian clock genes, which correlated with altered gene expression. We show that developmental CRD affects the circadian system and predisposes to non-communicable disease in adult life.

摘要

昼夜节律紊乱(CRD)会增加疾病的风险,例如代谢综合征、心血管疾病和癌症。在本研究中,我们研究了妊娠期反复时差导致的晚年不良健康影响。怀孕的老鼠接受了正常的明暗周期(CTRL)或重复的延迟(DEL)或提前(ADV)时差方案。DEL 和 ADV 后代的体重增加均减少。ADV 后代的昼夜节律周期延长,并且在 DEL 和 ADV 后代中均观察到对时差的反应改变。对成年雄性 ADV 后代的骨骼分析显示皮质骨量和强度降低。引人注目的是,对心脏的分析确定了结构异常和心脏功能受损。最后,DNA 甲基化分析显示 miR17-92 簇的过度甲基化和昼夜节律钟基因内的差异甲基化,这与改变的基因表达相关。我们表明,发育性 CRD 会影响昼夜节律系统,并使成年后易患非传染性疾病。

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