Contreras Raian E, Schriever Sonja C, Pfluger Paul T
Research Unit Neurobiology of Diabetes, Helmholtz Zentrum München, Neuherberg, Germany.
Institute for Diabetes and Obesity, Helmholtz Zentrum München, Neuherberg, Germany.
Front Genet. 2019 Dec 11;10:1015. doi: 10.3389/fgene.2019.01015. eCollection 2019.
Obesity and being overweight have become a worldwide epidemic affecting more than 1.9 billion adults and 340 million children. Efforts to curb this global health burden by developing effective long-term non-surgical weight loss interventions continue to fail due to weight regain after weight loss. Weight cycling, often referred to as Yoyo dieting, is driven by physiological counter-regulatory mechanisms that aim at preserving energy, decreased energy expenditure, increased energy intake, and impaired brain-periphery communication. Models based on genetically determined set points explained some of the weight control mechanisms, but exact molecular underpinnings remained elusive. Today, gene-environment interactions begin to emerge as likely drivers for the obesogenic memory effect associated with weight cycling. Here, epigenetic mechanisms, including histone modifications and DNA methylation, appear as likely factors that underpin long-lasting deleterious adaptations or an imprinted obesogenic memory to prevent weight loss maintenance. The first part summarizes our current knowledge on the physiology of weight cycling by discussing human and murine studies on the Yoyo-dieting phenomenon and physiological adaptations associated with weight loss and weight re-gain. The second part provides an overview on known associations between obesity and epigenetic modifications. We further interrogate the roles of epigenetic mechanisms in the CNS control of cognitive functions as well as reward and addictive behaviors, and subsequently discuss whether such mechanisms play a role in weight control. The final two parts describe major opportunities and challenges associated with studying epigenetic mechanisms in the CNS with its highly heterogenous cell populations, and provide a summary of recent technological advances that will help to delineate whether an obese memory is based upon epigenetic mechanisms.
肥胖和超重已成为一种全球性流行病,影响着超过19亿成年人和3.4亿儿童。由于减肥后体重反弹,通过开发有效的长期非手术减肥干预措施来控制这一全球健康负担的努力持续失败。体重循环,通常被称为溜溜球节食,是由旨在保存能量的生理反调节机制驱动的,包括能量消耗减少、能量摄入增加以及大脑与外周之间的通讯受损。基于基因决定的设定点的模型解释了一些体重控制机制,但确切的分子基础仍然难以捉摸。如今,基因-环境相互作用开始成为与体重循环相关的致肥胖记忆效应的可能驱动因素。在这里,表观遗传机制,包括组蛋白修饰和DNA甲基化,似乎是导致长期有害适应或印记致肥胖记忆以阻止体重减轻维持的可能因素。第一部分通过讨论关于溜溜球节食现象以及与体重减轻和体重恢复相关的生理适应的人体和小鼠研究,总结了我们目前对体重循环生理学的认识。第二部分概述了肥胖与表观遗传修饰之间的已知关联。我们进一步探讨了表观遗传机制在中枢神经系统对认知功能以及奖赏和成瘾行为的控制中的作用,随后讨论了这些机制是否在体重控制中发挥作用。最后两部分描述了在具有高度异质细胞群体的中枢神经系统中研究表观遗传机制所面临的主要机遇和挑战,并总结了近期的技术进展,这些进展将有助于确定肥胖记忆是否基于表观遗传机制。