Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York 10461, USA.
Endocrinology. 2012 Mar;153(3):1031-8. doi: 10.1210/en.2011-1805. Epub 2012 Jan 17.
A growing body of evidence suggests that the intrauterine (IU) environment has a significant and lasting effect on the long-term health of the growing fetus and the development of metabolic disease in later life as put forth in the fetal origins of disease hypothesis. Metabolic diseases have been associated with alterations in the epigenome that occur without changes in the DNA sequence, such as cytosine methylation of DNA, histone posttranslational modifications, and micro-RNA. Animal models of epigenetic modifications secondary to an altered IU milieu are an invaluable tool to study the mechanisms that determine the development of metabolic diseases, such as diabetes and obesity. Rodent and nonlitter bearing animals are good models for the study of disease, because they have similar embryology, anatomy, and physiology to humans. Thus, it is feasible to monitor and modify the IU environment of animal models in order to gain insight into the molecular basis of human metabolic disease pathogenesis. In this review, the database of PubMed was searched for articles published between 1999 and 2011. Key words included epigenetic modifications, IU growth retardation, small for gestational age, animal models, metabolic disease, and obesity. The inclusion criteria used to select studies included animal models of epigenetic modifications during fetal and neonatal development associated with adult metabolic syndrome. Experimental manipulations included: changes in the nutritional status of the pregnant female (calorie-restricted, high-fat, or low-protein diets during pregnancy), as well as the father; interference with placenta function, or uterine blood flow, environmental toxin exposure during pregnancy, as well as dietary modifications during the neonatal (lactation) as well as pubertal period. This review article is focused solely on studies in animal models that demonstrate epigenetic changes that are correlated with manifestation of metabolic disease, including diabetes and/or obesity.
越来越多的证据表明,宫内(IU)环境对胎儿的长期健康和成年后代谢性疾病的发展具有重要而持久的影响,这就是疾病起源于胎儿的假说。代谢性疾病与表观基因组的改变有关,这些改变发生在 DNA 序列不变的情况下,例如 DNA 中的胞嘧啶甲基化、组蛋白翻译后修饰和 micro-RNA。由于 IU 环境改变而导致的表观遗传修饰的动物模型是研究决定代谢性疾病(如糖尿病和肥胖症)发展的机制的宝贵工具。啮齿动物和非产仔动物是研究疾病的良好模型,因为它们的胚胎学、解剖学和生理学与人类相似。因此,监测和改变动物模型的 IU 环境以深入了解人类代谢性疾病发病机制是可行的。在这篇综述中,我们在 PubMed 数据库中搜索了 1999 年至 2011 年期间发表的文章。关键词包括表观遗传修饰、宫内生长迟缓、小于胎龄儿、动物模型、代谢性疾病和肥胖。选择研究的纳入标准包括与成年代谢综合征相关的胎儿和新生儿发育过程中表观遗传修饰的动物模型。实验操作包括:改变孕妇的营养状况(怀孕期间限制热量、高脂肪或低蛋白饮食),以及父亲的营养状况;干扰胎盘功能或子宫血流、怀孕期间暴露于环境毒素,以及新生儿(哺乳期)和青春期的饮食改变。这篇综述文章仅关注在动物模型中显示与代谢性疾病(包括糖尿病和/或肥胖)表现相关的表观遗传变化的研究。