Diabetes and Obesity Center of Excellence, Department of Medicine, University of Washington School of Medicine, South Lake Union, 815 Mercer Street, N334, Box 358055, Seattle, Washington 98109, USA.
J Clin Endocrinol Metab. 2012 Mar;97(3):745-55. doi: 10.1210/jc.2011-2525. Epub 2012 Jan 11.
Obesity has emerged as one of the leading medical challenges of the 21st century. The resistance of this disorder to effective, long-term treatment can be traced to the fact that body fat stores are subject to homeostatic regulation in obese individuals, just as in lean individuals. Because the growing obesity epidemic is linked to a substantial increase in daily energy intake, a key priority is to delineate how mechanisms governing food intake and body fat content are altered in an obesogenic environment.
We considered all relevant published research and cited references that represented the highest quality evidence available. Where space permitted, primary references were cited.
The increase of energy intake that has fueled the U.S. obesity epidemic is linked to greater availability of highly rewarding/palatable and energy-dense food. Obesity occurs in genetically susceptible individuals and involves the biological defense of an elevated body fat mass, which may result in part from interactions between brain reward and homeostatic circuits. Inflammatory signaling, accumulation of lipid metabolites, or other mechanisms that impair hypothalamic neurons may also contribute to the development of obesity and offer a plausible mechanism to explain the biological defense of elevated body fat mass.
Despite steady research progress, mechanisms underlying the resistance to fat loss once obesity is established remain incompletely understood. Breakthroughs in this area may be required for the development of effective new obesity prevention and treatment strategies.
肥胖已成为 21 世纪主要的医学挑战之一。这种疾病对有效、长期治疗的抵抗力可以追溯到这样一个事实,即肥胖个体的体脂肪储存受到体内平衡调节,就像瘦个体一样。由于日益严重的肥胖症与每日能量摄入的大量增加有关,因此当务之急是阐明在致肥胖环境中,控制食物摄入和体脂肪含量的机制是如何发生改变的。
我们考虑了所有相关的已发表研究和引用的参考文献,这些参考文献代表了现有最高质量的证据。在有空间的情况下,引用了主要参考文献。
推动美国肥胖流行的能量摄入增加与更大量的高奖励/美味和高能量食物的供应有关。肥胖发生在易患遗传个体中,并涉及升高的体脂肪量的生物学防御,这可能部分是由于大脑奖励和体内平衡回路之间的相互作用所致。炎症信号、脂质代谢物的积累或其他损害下丘脑神经元的机制也可能导致肥胖的发生,并提供了一种合理的机制来解释升高的体脂肪量的生物学防御。
尽管研究进展稳定,但一旦肥胖确立,导致脂肪减少的抵抗机制仍不完全清楚。在这一领域取得突破可能是制定有效新的肥胖预防和治疗策略所必需的。