Cano Lucía Carolina, Navarrete Erika, Ochoa-Romo Juan Pablo, Díaz Georgina, Díaz-Hernández Verónica, Montúfar-Chaveznava Rodrigo, Caldelas Ivette
Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.
Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.
Biology (Basel). 2025 May 13;14(5):541. doi: 10.3390/biology14050541.
In mammals, the core molecular clock genes and the overall circadian system are established during early development; during this critical period of development, maternal metabolic condition plays a major role in programming temporal metabolic regulation. Therefore, this study aimed to evaluate the effects of the chronic maternal intake of a high-fat and high-carbohydrate diet (HFCD) before and during pregnancy, in addition to a challenge with HFCD during adulthood, on offspring diurnal metabolic profile and on clock gene expression in central and peripheral circadian oscillators. The HFCD offspring and/or those exposed to the metabolic challenge exhibited alterations in the temporal profiles of analytes associated with both the carbohydrate and lipid metabolisms, as well as markers associated with liver and kidney damage, ranging from phase changes in rhythmicity or, in some cases, to the complete loss of 24 h variations. At the molecular level, the expression of clock genes (, , , and ) in the central and peripheral oscillators showed differential susceptibility to undergoing changes in their abundance. Our data indicate that maternal HFCD during pregnancy, a second exposure in adulthood, or both result in the long-term misalignment of the diurnal rhythm's metabolic and damage markers; these changes are possibly associated with alterations in the core molecular circadian clockwork.
在哺乳动物中,核心分子时钟基因和整体昼夜节律系统在早期发育过程中建立;在这个关键的发育时期,母体代谢状况在编程时间代谢调节中起主要作用。因此,本研究旨在评估孕期及孕期前长期摄入高脂高碳水化合物饮食(HFCD),以及成年期接受HFCD刺激,对后代昼夜代谢谱以及中枢和外周昼夜节律振荡器中时钟基因表达的影响。HFCD组后代和/或暴露于代谢刺激的后代,在与碳水化合物和脂质代谢相关的分析物的时间分布上,以及与肝损伤和肾损伤相关的标志物上均表现出改变,范围从节律性的相位变化,在某些情况下,到24小时变化的完全丧失。在分子水平上,中枢和外周振荡器中时钟基因( 、 、 、和 )的表达在丰度变化方面表现出不同的敏感性。我们的数据表明,孕期母体摄入HFCD、成年期再次暴露或两者兼而有之,都会导致昼夜节律的代谢和损伤标志物长期失调;这些变化可能与核心分子昼夜节律机制的改变有关。