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应激和奖励对大鼠前脑阿片肽能和 GABA 能回路的调节相互作用。

Regulatory interactions of stress and reward on rat forebrain opioidergic and GABAergic circuitry.

机构信息

Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati, 2170 E. Galbraith Road, Reading, OH 45237-0506, USA.

出版信息

Stress. 2011 Mar;14(2):205-15. doi: 10.3109/10253890.2010.531331.

Abstract

Palatable food intake reduces stress responses, suggesting that individuals may consume such ?comfort? food as self-medication for stress relief. The mechanism by which palatable foods provide stress relief is not known, but likely lies at the intersection of forebrain reward and stress regulatory circuits. Forebrain opioidergic and gamma-aminobutyric acid ergic signaling is critical for both reward and stress regulation, suggesting that these systems are prime candidates for mediating stress relief by palatable foods. Thus, the present study (1) determines how palatable ?comfort? food alters stress-induced changes in the mRNA expression of inhibitory neurotransmitters in reward and stress neurocircuitry and (2) identifies candidate brain regions that may underlie comfort food-mediated stress reduction. We used a model of palatable ?snacking? in combination with a model of chronic variable stress followed by in situ hybridization to determine forebrain levels of pro-opioid and glutamic acid decarboxylase (GAD) mRNA. The data identify regions within the extended amygdala, striatum, and hypothalamus as potential regions for mediating hypothalamic-pituitary-adrenal axis buffering following palatable snacking. Specifically, palatable snacking alone decreased pro-enkephalin-A (ENK) mRNA expression in the anterior bed nucleus of the stria terminalis (BST) and the nucleus accumbens, and decreased GAD65 mRNA in the posterior BST. Chronic stress alone increased ENK mRNA in the hypothalamus, nucleus accumbens, amygdala, and hippocampus; increased dynorphin mRNA in the nucleus accumbens; increased GAD65 mRNA in the anterior hypothalamus and BST; and decreased GAD65 mRNA in the dorsal hypothalamus. Importantly, palatable food intake prevented stress-induced gene expression changes in subregions of the hypothalamus, BST, and nucleus accumbens. Overall, these data suggest that complex interactions exist between brain reward and stress pathways and that palatable snacking can mitigate many of the neurochemical alterations induced by chronic stress.

摘要

可口的食物摄入可减轻应激反应,表明个体可能会将这种“舒适”食物作为缓解压力的自我治疗方法。目前尚不清楚美味食物缓解压力的机制,但可能存在于大脑前奖励和应激调节回路的交汇处。大脑前阿片和γ-氨基丁酸能信号对于奖励和应激调节都至关重要,这表明这些系统是美味食物缓解压力的主要候选途径。因此,本研究(1)确定美味的“舒适”食物如何改变奖励和应激神经回路中应激诱导的抑制性神经递质的 mRNA 表达变化,以及(2)确定可能是舒适食物介导的应激减轻的潜在脑区。我们使用美味的“小吃”模型与慢性可变应激模型相结合,然后进行原位杂交,以确定前脑的前阿片原和谷氨酸脱羧酶 (GAD) mRNA 水平。这些数据确定了扩展杏仁核、纹状体和下丘脑内的潜在区域,这些区域可能是调节下丘脑-垂体-肾上腺轴缓冲作用的区域,这些区域是在美味小吃后进行的。具体而言,单独食用美味小吃可降低终纹床核前部(BST)和伏隔核中的前脑啡肽-A (ENK) mRNA 表达,并降低 BST 后部的 GAD65 mRNA。单独的慢性应激会增加下丘脑、伏隔核、杏仁核和海马中的 ENK mRNA;增加伏隔核中的强啡肽 mRNA;增加前下丘脑和 BST 中的 GAD65 mRNA;并减少背侧下丘脑的 GAD65 mRNA。重要的是,美味食物的摄入可防止下丘脑、BST 和伏隔核亚区的应激诱导的基因表达变化。总的来说,这些数据表明,大脑奖励和应激途径之间存在复杂的相互作用,美味小吃可以减轻慢性应激引起的许多神经化学变化。

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