Pathways linking the early environment to long-term health and lifespan

被引:103
作者
Barnes, S. K. [1 ]
Ozanne, S. E. [1 ]
机构
[1] Univ Cambridge, Metab Res Labs, Addenbrookes Hosp, Inst Metab Sci, Cambridge CB2 0QQ, England
基金
英国生物技术与生命科学研究理事会;
关键词
Early growth; Maternal diet; Epigenetics; Oxidative stress; Hormesis; Caloric restriction; MATERNAL PROTEIN RESTRICTION; LOW-BIRTH-WEIGHT; INTRAUTERINE GROWTH-RETARDATION; CATCH-UP GROWTH; IMPAIRED OXIDATIVE-PHOSPHORYLATION; BETA-HYDROXYSTEROID DEHYDROGENASE; RENIN-ANGIOTENSIN SYSTEM; SYSTOLIC BLOOD-PRESSURE; CORONARY-HEART-DISEASE; DIET-INDUCED OBESITY;
D O I
10.1016/j.pbiomolbio.2010.12.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The intrauterine environment is a major contributor to normal physiological growth and development of an individual. Disturbances at this critical time can affect the long-term health of the offspring. Low birth weight individuals have strong correlations with increased susceptibility to type 2 diabetes and cardiovascular disease in later-life. These observations led to the Thrifty Phenotype Hypothesis which suggested that these associations arose because of the response of a growing fetus to a suboptimal environment such as poor nutrition. Animal models have shown that environmentally induced intrauterine growth restriction increases the risk of a variety of diseases later in life. These detrimental features are also observed in high birth weight offspring from mothers who were obese or consumed a high fat diet during gestation. Recent advances in our understanding of the mechanisms underlying this phenomenon have elucidated several potential candidates for the long-term effects of the early environment on the function and metabolism of a cell. These include: (1) Epigenetic alterations (e.g. DNA methylation and histone modifications), which regulate specific gene expression and can be influenced by the environment, both during gestation and early postnatal life and (2) Oxidative stress that changes the balance between reactive oxygen species generation (e.g. through mitochondrial dysfunction) and antioxidant defense capacity. This has permanent effects on cellular ageing such as regulation of telomere length. Further understanding of these processes will help in the development of therapeutic strategies to increase healthspan and reduced the burden of age-associated diseases. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:323 / 336
页数:14
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