Carr Kenneth D
Departments of Psychiatry, and Biochemistry and Molecular Pharmacology, New York University School of Medicine, 550 First Avenue, New York, New York 10016.
Curr Opin Behav Sci. 2016 Jun;9:32-39. doi: 10.1016/j.cobeha.2015.11.019.
There is a high rate of comorbidity between eating disorders and substance abuse, and specific evidence that weight-loss dieting can increase risk for binge pathology, rebound excessive weight gain, and initiation and relapse to drug abuse. The present overview discusses basic science findings indicating that chronic food restriction induces dopamine conservation, compensatory upregulation of D-1 dopamine receptor signaling, and synaptic incorporation of calcium-permeable glutamatergic AMPA receptors in nucleus accumbens. Evidence is presented which indicates that these neuroadaptations account for increased incentive effects of food, drugs, and associated environments during food restriction. In addition, these same neuroadaptations underlie upregulation of sucrose- and psychostimulant-induced trafficking of AMPA receptors to the nucleus accumbens postsynaptic density, which may be a mechanistic basis of enduring maladaptive behavior.
饮食失调与药物滥用之间存在很高的共病率,并且有具体证据表明,减肥节食会增加暴饮暴食病理、体重过度反弹以及药物滥用起始和复发的风险。本综述讨论了基础科学研究结果,这些结果表明长期食物限制会导致多巴胺保存、D-1多巴胺受体信号的代偿性上调,以及伏隔核中钙通透性谷氨酸能AMPA受体的突触整合。有证据表明,这些神经适应性变化解释了在食物限制期间食物、药物及相关环境的激励作用增强的原因。此外,这些相同的神经适应性变化也是蔗糖和精神兴奋剂诱导的AMPA受体向伏隔核突触后致密区转运上调的基础,这可能是持久适应不良行为的机制基础。