Gali Ramamoorthy Thanuja, Begum Ghazala, Harno Erika, White Anne
Faculty of Life Sciences, University of Manchester Manchester, UK.
School of Clinical and Experimental Medicine, University of Birmingham Birmingham, UK.
Front Neurosci. 2015 Apr 21;9:126. doi: 10.3389/fnins.2015.00126. eCollection 2015.
The prevalence of obesity in adults and children has increased globally at an alarming rate. Mounting evidence from both epidemiological studies and animal models indicates that adult obesity and associated metabolic disorders can be programmed by intrauterine and early postnatal environment- a phenomenon known as "fetal programming of adult disease." Data from nutritional intervention studies in animals including maternal under- and over-nutrition support the developmental origins of obesity and metabolic syndrome. The hypothalamic neuronal circuits located in the arcuate nucleus controlling appetite and energy expenditure are set early in life and are perturbed by maternal nutritional insults. In this review, we focus on the effects of maternal nutrition in programming permanent changes in these hypothalamic circuits, with experimental evidence from animal models of maternal under- and over-nutrition. We discuss the epigenetic modifications which regulate hypothalamic gene expression as potential molecular mechanisms linking maternal diet during pregnancy to the offspring's risk of obesity at a later age. Understanding these mechanisms in key metabolic genes may provide insights into the development of preventative intervention strategies.
全球范围内,成人和儿童肥胖症的患病率正以惊人的速度上升。来自流行病学研究和动物模型的越来越多的证据表明,成人肥胖症及相关代谢紊乱可能由子宫内和出生后早期环境所编程——这一现象被称为“成人疾病的胎儿编程”。来自动物营养干预研究的数据,包括母体营养不足和营养过剩,支持了肥胖症和代谢综合征的发育起源。位于弓状核控制食欲和能量消耗的下丘脑神经回路在生命早期就已设定,并会因母体营养损伤而受到干扰。在这篇综述中,我们聚焦于母体营养对这些下丘脑回路永久性变化编程的影响,并给出母体营养不足和营养过剩动物模型的实验证据。我们讨论了调节下丘脑基因表达的表观遗传修饰,将其作为将孕期母体饮食与后代晚年肥胖风险联系起来的潜在分子机制。了解关键代谢基因中的这些机制,可能为预防性干预策略的制定提供思路。