Obesogens, stem cells and the developmental programming of obesity

A. Janesick, B. Blumberg
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引用次数: 124

Abstract

Obesogens are chemicals that directly or indirectly lead to increased fat accumulation and obesity. Obesogens have the potential to disrupt multiple metabolic signalling pathways in the developing organism that can result in permanent changes in adult physiology. Prenatal or perinatal exposure to obesogenic endocrine disrupting chemicals has been shown to predispose an organism to store more fat from the beginning of its life. For example, excess oestrogen or cortisol exposure in the womb or during early life resulted in an increased susceptibility to obesity and metabolic syndrome later in life. This review focuses on the effects of environmental chemicals, such as the model obesogen, tributyltin (TBT), on the development of obesity. We discuss evidence linking the obesogenic effects of TBT with its ability to activate the peroxisome proliferator-activated receptor gamma and stimulate adipogenesis. We also discuss how TBT and other environmental obesogens may lead to epigenetic changes that predispose exposed individuals to subsequent weight gain and obesity. This suggests that humans, who have been exposed to obesogenic chemicals during sensitive windows of development, might be pre-programmed to store increased amounts of fat, resulting in a lifelong struggle to maintain a healthy weight and exacerbating the deleterious effects of poor diet and inadequate exercise.

肥胖原,干细胞和肥胖的发育程序
致肥物质是直接或间接导致脂肪堆积和肥胖的化学物质。肥胖原有可能破坏发育中生物体的多种代谢信号通路,从而导致成人生理的永久性变化。产前或围产期接触致肥性内分泌干扰化学物质已被证明会使生物体从生命开始就倾向于储存更多脂肪。例如,在子宫内或生命早期暴露过多的雌激素或皮质醇会导致以后更容易肥胖和代谢综合征。本文综述了环境化学物质对肥胖发展的影响,如模型致肥源三丁基锡(TBT)。我们讨论了将TBT的致肥作用与其激活过氧化物酶体增殖物激活受体γ和刺激脂肪生成的能力联系起来的证据。我们还讨论了TBT和其他环境致肥源如何导致表观遗传变化,从而使暴露个体易患随后的体重增加和肥胖。这表明,在发育的敏感窗口期暴露于致肥化学物质的人类,可能被预先设定为储存更多的脂肪,导致一生都在努力保持健康的体重,并加剧了不良饮食和运动不足的有害影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
0.00%
发文量
200
审稿时长
6-12 weeks
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