Liggins Institute and Gravida, National Centre for Growth and Development, University of Auckland, 85 Park Road, Grafton, Auckland 1142, New Zealand.
Nutrients. 2014 Jun 2;6(6):2165-78. doi: 10.3390/nu6062165.
The global pandemic of obesity and type 2 diabetes is often causally linked to marked changes in diet and lifestyle; namely marked increases in dietary intakes of high energy diets and concomitant reductions in physical activity levels. However, less attention has been paid to the role of developmental plasticity and alterations in phenotypic outcomes resulting from altered environmental conditions during the early life period. Human and experimental animal studies have highlighted the link between alterations in the early life environment and increased risk of obesity and metabolic disorders in later life. This link is conceptualised as the developmental programming hypothesis whereby environmental influences during critical periods of developmental plasticity can elicit lifelong effects on the health and well-being of the offspring. In particular, the nutritional environment in which the fetus or infant develops influences the risk of metabolic disorders in offspring. The late onset of such diseases in response to earlier transient experiences has led to the suggestion that developmental programming may have an epigenetic component, as epigenetic marks such as DNA methylation or histone tail modifications could provide a persistent memory of earlier nutritional states. Moreover, evidence exists, at least from animal models, that such epigenetic programming should be viewed as a transgenerational phenomenon. However, the mechanisms by which early environmental insults can have long-term effects on offspring are relatively unclear. Thus far, these mechanisms include permanent structural changes to the organ caused by suboptimal levels of an important factor during a critical developmental period, changes in gene expression caused by epigenetic modifications (including DNA methylation, histone modification, and microRNA) and permanent changes in cellular ageing. A better understanding of the epigenetic basis of developmental programming and how these effects may be transmitted across generations is essential for the implementation of initiatives aimed at curbing the current obesity and diabetes crisis.
全球肥胖和 2 型糖尿病的流行通常与饮食和生活方式的显著变化有关;即饮食中高热量食物的摄入量显著增加,同时体力活动水平降低。然而,人们对发育可塑性的作用以及生命早期环境改变导致表型结果改变的关注较少。人类和实验动物研究强调了生命早期环境改变与肥胖和代谢紊乱风险增加之间的联系。这种联系被概念化为发育编程假说,即在发育可塑性的关键时期,环境影响可以对后代的健康和幸福产生终身影响。特别是,胎儿或婴儿发育过程中的营养环境会影响后代患代谢紊乱的风险。由于早期短暂的经历导致这些疾病的晚期发病,因此有人提出发育编程可能具有表观遗传成分,因为表观遗传标记,如 DNA 甲基化或组蛋白尾部修饰,可以提供早期营养状态的持久记忆。此外,至少从动物模型中可以得到证据,这种表观遗传编程应该被视为一种跨代现象。然而,早期环境损伤如何对后代产生长期影响的机制尚不清楚。到目前为止,这些机制包括在关键发育时期重要因素水平不足时对器官造成的永久性结构变化、表观遗传修饰(包括 DNA 甲基化、组蛋白修饰和 microRNA)引起的基因表达变化以及细胞衰老的永久性变化。更好地理解发育编程的表观遗传基础以及这些影响如何在代际之间传递,对于实施旨在遏制当前肥胖和糖尿病危机的举措至关重要。