Persistent effects of obesity: a neuroplasticity hypothesis

被引:47
作者
Matikainen-Ankney, Bridget A. [1 ]
Kravitz, Alexxai V. [1 ,2 ]
机构
[1] NIDDK, NIH, Bldg 10 CRC,Room 5-5932,10 Ctr Dr, Bethesda, MD 20814 USA
[2] NIAAA, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
obesity; plasticity; synaptic; glutamate; high-fat diet; HIGH-FAT-DIET; VENTRAL TEGMENTAL AREA; LONG-TERM POTENTIATION; DOPAMINE D2 RECEPTOR; MU-OPIOID RECEPTOR; NUCLEUS-ACCUMBENS SHELL; GLUR2-LACKING AMPA RECEPTORS; GASTRIC BYPASS-SURGERY; BODY-MASS INDEX; MESOLIMBIC DOPAMINE;
D O I
10.1111/nyas.13665
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The obesity epidemic is a leading cause of health problems in the United States, increasing the risk of cardiovascular, endocrine, and psychiatric diseases. Although many people lose weight through changes in diet and lifestyle, keeping the weight off remains a challenge. Here, we discuss a hypothesis that seeks to explain why obesity is so persistent. There is a great degree of overlap in the circuits implicated in substance use disorder and obesity, and neural plasticity of these circuits in response to drugs of abuse is well documented. We hypothesize that obesity is also associated with neural plasticity in these circuits, and this may underlie persistent changes in behavior, energy balance, and body weight. Here, we discuss how obesity-associated reductions in motivation and physical activity may be rooted in neurophysiological alterations in these circuits. Such plasticity may alter how humans and animals use, expend, and store energy, even after weight loss.
引用
收藏
页码:221 / 239
页数:19
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